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UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

FORM 10-Q

(Mark One)

☒ QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For the quarterly period ended ~~March~~June 3130, 2025

☐ TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For the transition period from to

Commission File Number 001-41245

~~CONDUIT PHARMACEUTICALS~~CDT EQUITY INC.

(Exact name of registrant as specified in its charter)

Delaware		87-3272543
(State or other jurisdiction of incorporation or organization)		(I.R.S. Employer Identification No.)
4581 Tamiami Trail North, Suite 200 Naples, Florida		34103
(Address of Principal Executive Offices)		(Zip Code

(646) 491-9132 (Registrant’s telephone number, including area code) N/A (Former name, former address and former fiscal year, if changed since last report)

4581 Tamiami Trail North, Suite 200 Naples, Florida		34103
(Address of Principal Executive Offices)		(Zip Code)

(646) 491-9132

(Registrant’s telephone number, including area code)

Conduit Pharmaceuticals, Inc.

(Former name, former address and former fiscal year, if changed since last report)

Securities registered pursuant to Section 12(b) of the Act:

Title of each class	Trading Symbol(s)	Name of each exchange on which registered
Common Stock, par value $0.0001 per share	CDT	The Nasdaq Stock Market LLC
Redeemable Warrants, each whole warrant exercisable for one share of Common Stock at an exercise price of $1,150.00	CDTTW	The Nasdaq Stock Market LLC
Redeemable Warrants, each whole warrant exercisable for one share of Common Stock at an exercise price of $17,250.00	CDTTW	The Nasdaq Stock Market LLC

Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days. Yes ☒ No ☐

Indicate by check mark whether the registrant has submitted electronically every Interactive Data File required to be submitted pursuant to Rule 405 of Regulation S-T (§232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit such files). Yes ☒ No ☐

Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, a smaller reporting company, or an emerging growth company. See the definitions of “large accelerated filer,” “accelerated filer,” “smaller reporting company,” and “emerging growth company” in Rule 12b-2 of the Exchange Act.

☐ Large accelerated filer	☐ Accelerated filer
☒ Non-accelerated filer	☒ Smaller reporting company
	☒ Emerging growth company

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐

Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act): Yes ☐ No ☒

As of ~~May~~August 14, 2025, there were 113,~~961~~062,~~460~~ 025 shares of common stock, $0.0001 par value (the “Common Stock”) of the registrant issued and outstanding.

~~CONDUIT PHARMACEUTICALS~~CDT EQUITY INC.

Form 10-Q

Table of Contents

		~~Page~~	Page
Part I-Financial Information.
Item 1.	Financial Statements.		1
	Condensed Consolidated Balance Sheets as of March 31, 2025 (unaudited) and December 31, 2024 (audited).	1
	Condensed Consolidated Balance Sheets as of June 30, 2025 (unaudited) and December 31, 2024 (audited).		1
	Unaudited Condensed Consolidated Statements of Operations and Comprehensive Loss for the three months ended March 31, 2025 and 2024.	2
	Unaudited Condensed Consolidated Statements of Operations and Comprehensive Loss for the three and six months ended June 30, 2025 and 2024.		2
	Unaudited Condensed Consolidated Statements of Changes in Stockholders’ Equity (Deficit) for the three months ended March 31, 2025 and 2024.	3
	Unaudited Condensed Consolidated Statements of Changes in Stockholders’ Deficit for the three and six months ended June 30, 2025 and 2024.		3
	Unaudited Condensed Consolidated Statements of Cash Flows for the three months ended March 31, 2025 and 2024.	4
	Unaudited Condensed Consolidated Statement of Cash Flows for the six months ended June 30, 2025 and 2024.		4
	Notes to Unaudited Condensed Consolidated Financial Statements.	5	5
Item 2.	Management’s Discussion and Analysis of Financial Condition and Results of Operations.	29	31
Item 3.	Quantitative and Qualitative Disclosures About Market Risk.	37	41
Item 4.	Controls and Procedures.	37	41
Part II-Other Information.
Item 1.	Legal Proceedings.	38	42
Item 1A.	Risk Factors.	38	42
Item 2.	Unregistered Sales of Equity Securities and Use of Proceeds.	38	42
Item 3.	Defaults Upon Senior Securities.	38	42
Item 4.	Mine Safety Disclosures.	38	42
Item 5.	Other Information.	38	42
Item 6.	Exhibits.	39	43
Part III-Signatures.		40	44

CAUTIONARY STATEMENT REGARDING FORWARD-LOOKING STATEMENTS

This Quarterly Report on Form 10-Q (this “Quarterly Report”) for the quarterly period ended ~~March~~June 3130, 2025 contains forward-looking statements. Forward-looking statements are neither historical facts nor assurances of future performance. Instead, they are based only on our current beliefs, expectations, and assumptions regarding the future of our business, future plans and strategies, projections, anticipated events and trends, the economy, and other future conditions. This includes, without limitation, statements regarding the financial position and the plans and objectives of management for our future operations. Such statements can be identified by the fact that they do not relate strictly to historical or current facts. When used in this Quarterly Report, words such as “anticipate,” “believe,” “continue,” “could,” “estimate,” “expect,” “intend,” “may,” “might,” “plan,” “possible,” “potential,” “predict,” “project,” “should,” “strive,” “would” and similar expressions may identify forward-looking statements, but the absence of these words does not mean that a statement is not forward-looking. Factors that could materially affect our business operations and financial performance and condition include, but are not limited to, those risks and uncertainties described herein under “Item 1A. Risk Factors,” those described in our Annual Report on Form 10-K for the year ended December 31, 2024, under “Item 1A. Risk Factors,” filed with the U.S. Securities and Exchange Commission (the “SEC”). You are urged to consider these factors carefully in evaluating the forward-looking statements and are cautioned not to place undue reliance on the forward-looking statements. The forward-looking statements are based on information available to us as of the filing date of this Quarterly Report. Unless required by law, we do not intend to publicly update or revise any forward-looking statements to reflect new information or future events or otherwise. You should, however, review the risk factors we describe in the reports we will file from time to time with the SEC after the date of this Quarterly Report.

This Quarterly Report may also contain market data related to our business and industry. These market data include projections that are based on a number of assumptions. If these assumptions turn out to be incorrect, actual results may differ from the projections based on these assumptions. As a result, our markets may not grow at the rates projected by these data, or at all. The failure of these markets to grow at these projected rates may harm our business, results of operations, financial condition, and the market price of our ~~common~~Common ~~stock~~Stock.

PART I-FINANCIAL INFORMATION

Item 1. Financial Statements.

~~CONDUIT PHARMACEUTICALS~~CDT EQUITY INC.

CONDENSED CONSOLIDATED BALANCE SHEETS

(in thousands, except share and per share amounts)

	March 31, 2025 (Unaudited)			December 31, 2024 (Audited)
	June 30, 2025 (Unaudited)			December 31, 2024 (Audited)
ASSETS
Current assets
Cash and cash equivalents	$	23,~~130~~332		$	554
Prepaid R&D services- related party (see Note 7 and Note 12)		1,814			380
Prepaid R&D services- related party (see Note 6 and Note 11)		1,626			380
Prepaid R&D services (see Note 7)		279			-
Prepaid R&D services (see Note 6)		140			-
Prepaid expenses and other current assets		1,~~726~~288			1,781
Total current assets		56,~~949~~386			2,715
Operating lease right-of-use assets. net		234			263
Operating lease right-of-use assets, net		204			263
Property, plant and equipment, net		41			40
Equipment and clinical assets, net		381			40
Prepaid expenses and other long-term assets		1,~~097~~018			1,175
Total assets	$	7,~~321~~989		$	4,193
LIABILITIES AND STOCKHOLDERS’ EQUITY (DEFICIT)
Current liabilities
Accounts payable	$	~~714~~1,253		$	1,428
Accrued expenses and other current liabilities		1,~~045~~140			1,963
Operating lease liability, current portion		~~126~~138			119
Convertible promissory note payable		-			800
Convertible promissory notes payable at fair value		21,~~663~~882			2,985
Convertible promissory notes payable at fair value – related parties		-			2,871
Convertible promissory notes payable at fair value		-			2,871
Notes payable		-			150
Notes payable – related parties		-			425
Notes payable		-			425
Total current liabilities		4,~~548~~413			10,741
Operating lease liability, non-current portion		7846			107
Derivative warrant liability		81			138
Total liabilities		4,~~634~~460			10,986
Commitments and contingencies (see Note 15)		-			-
Commitments and contingencies (see Note 14)		-			-
Stockholders’ equity (deficit)
Common stock, par value $0.0001; 250,000,000 shares authorized at March 31, 2025 and December 31, 2024, respectively, 9,512,058 shares and 1,384,801 shares issued and outstanding at March 31, 2025 and December 31, 2024, respectively		19			14
Common stock, par value $0.0001; 250,000,000 shares authorized at June 30, 2025 and December 31, 2024, respectively, 2,405,129 shares and 92,320 shares issued at June 30, 2025 and December 31, 2024, respectively, and 2,393,416 and 92,320 shares outstanding at June 30, 2025 and December 31, 2024, respectively		-			-
Preferred stock, par value $0.0001; 1,000,000 shares authorized at March 31, 2025 and December 31, 2024, respectively; nil shares issued and outstanding at March 31, 2025 and December 31, 2024		-			-
Preferred stock, par value $0.0001; 1,000,000 shares authorized at June 30, 2025 and December 31, 2024, respectively; nil shares issued and outstanding at June 30, 2025 and December 31, 2024		-			-
Additional paid-in capital		3643,~~569~~248			21,~~880~~894
Accumulated deficit		(34,247	)		(29,101	)
Treasury stock; 11,713 shares and nil shares issued at June 30, 2025 and December 31, 2024, respectively, at cost		(106	)		-
Accumulated other comprehensive income		346			414
Accumulated deficit		(39,882	)		(29,101	)
Total stockholders’ equity (deficit)		2,687			(6,793	)
Accumulated other comprehensive income		269			414
Total liabilities and stockholders’ equity (deficit)	$	7,321		$	4,193
Total stockholders’ equity (deficit)		3,529			(6,793	)
Total liabilities and stockholders’ equity (deficit)	$	7,989		$	4,193

The accompanying notes are an integral part of these condensed consolidated financial statements.

~~CONDUIT PHARMACEUTICALS~~CDT EQUITY INC.

CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS

(unaudited)

(in thousands, except share and per share amounts)

	2025			2024			2025			2024
	Three Months ended March 31,
	Three Months ended June 30,						Six Months ended June 30,
	2025			2024			2025			2024
Operating expenses:
Research and development expenses	$	1,~~309~~860		$	~~128~~25		$	2,776		$	153
General and administrative expenses		23,~~700~~092			23,~~827~~115			5,792			5,942
Total operating expenses		4,~~009~~952			23,~~955~~140			8,568			6,095
Operating loss		(4,~~009~~952	)		(23,~~955~~140	)		(8,568	)		(6,095	)
Other income (expense):
Other income (expense), net		(969	)		(487	)
Other expense, net		(1,023	)		(2,126	)		(1,992	)		(2,613	)
Interest income		84			92			12			11
Interest expense		(~~176~~57	)		(119	)		(233	)		(238	)
Total other (expense) income, net		(1,137	)		(597	)
Total other expense, net		(1,076	)		(2,243	)		(2,213	)		(2,840	)
Net loss	$	(56,~~146~~028	)	$	(35,~~552~~383	)	$	(10,781	)	$	(8,935	)
Basic and diluted net loss per share	$	(15.3246	)	$	(4109.8133	)	$	(15.77	)	$	(181.51	)
Basic weighted-average common shares outstanding		3,885,758			738,295
Basic and diluted weighted-average common shares outstanding		1,103,487			49,234			683,590			49,227
Diluted weighted-average common shares outstanding		3,885,758			738,295
Comprehensive loss:
Comprehensive loss:
Foreign currency translation adjustment		(77	)		(1	)		(145	)		(24	)
Foreign currency translation adjustment		(68	)		(23	)
Total comprehensive loss	$	(6,105	)	$	(5,384	)		(10,926	)	$	(8,959	)
Total comprehensive loss	$	(5,214	)	$	(3,575	)

The accompanying notes are an integral part of these condensed consolidated financial statements.

~~CONDUIT PHARMACEUTICALS~~CDT EQUITY INC.

CONDENSED CONSOLIDATED STATEMENTS OF CHANGES IN STOCKHOLDERS’ EQUITY ~~(DEFICIT)~~

(DEFICIT)

(unaudited)

(in thousands, except share amounts)

	Shares		Amount		~~capital~~Stock			~~deficit~~capital			~~income~~deficit			~~deficit~~income			deficit
	Common stock				~~Additional paid-in~~Treasury			~~Accumulated~~Additional paid-in			Accumulated ~~other comprehensive~~			~~Total~~Accumulated ~~stockholders’~~other ~~Equity~~comprehensive			Total stockholders’ equity
	Shares		Amount		~~capital~~Stock			~~deficit~~capital			~~income~~deficit			~~(deficit)~~income			(deficit)
Balance at January 1, 2025		1,384,801	$	14	$	21,880		$	(29,101	)	$	414		$	(6,793	)
Balance at April 1, 2025		634,137	$	-	$	-		$	36,588		$	(33,854	)	$	346		$	3,080
Issuance of common stock for services		2,450,191		1		2,211			-			-			2,212
Issuance of Common Stock for services		258,096		-		-			740			-			-			740
Issuance of common stock under the ATM program		4,345,866		1		8,167			-			-			8,168
Issuance of Common Stock under the ATM Program		1,183,221		-		-			3,887			-			-			3,887
Issuance of common stock upon exercise of conversion option		1,331,200		3		4,077			-			-			4,080
Issuance of Common Stock upon exercise of conversion option		329,692		-		-			1,873			-			-			1,873
Stock-based compensation		-		-		~~234~~-			-160			-			~~234~~-			160
Foreign currency translation adjustment		-		-		-			-			(68	)		(68	)
Share Repurchases		-		-		(106	)		-			-			-			(106	)
Net loss		-		-		-			(5,146	)		-			(5,146	)
Foreign currency translation adjustment		-		-		-			-			-			(77	)		(77	)
Balance at March 31, 2025		9,512,058		19		36,569			(34,247	)		346			2,687
Net loss		-		-		-			-			(6,028	)		-			(6,028	)
Balance at June 30, 2025		2,405,146	$	-	$	(106	)	$	43,248		$	(39,882	)	$	269		$	3,529

	Common stock				~~Additional paid-in~~Treasury			~~Accumulated~~Additional paid-in			Accumulated ~~other comprehensive~~			~~Total~~Accumulated ~~stockholders’~~other comprehensive			Total stockholders’ equity
	Shares		Amount		~~capital~~Stock			~~deficit~~capital			~~income~~deficit			~~deficit~~income			(deficit)
Balance at January 1, 2024		738,295	$	7	$	10,424		$	(11,299	)	$	411		$	(457	)
Balance at January 1, 2025		92,320	$	-	$	-		$	21,894		$	(29,101	)	$	414		$	(6,793	)
Balance		738,295	$	7	$	10,424		$	(11,299	)	$	411		$	(457	)
Issuance of Common Stock for services		421,442		-		-			2,952			-			-			2,952
Issuance of Warrants for lock-up		-		-		502			-			-			502
Issuance of Common Stock under the ATM Program		1,472,945		-		-			12,055			-			-			12,055
Stock-based compensation		-		-		431			-			-			431
Issuance of Common Stock upon exercise of conversion option		418,439		-		-			5,953			-			-			5,953
Foreign currency translation adjustment		-		-		-			-			(23	)		(23	)
Stock-based compensation		-		-		-			394			-			-			394
Net loss		-		-		-			(3,552	)		-			(3,552	)
Share Repurchases		-		-		(106	)		-			-			-			(106	)
Balance at March 31, 2024		738,295	$	7	$	11,357		$	(14,851	)	$	388		$	(3,099	)
Foreign currency translation adjustment		-		-		-			-			-			(145	)		(145	)
Balance		738,295	$	7	$	11,357		$	(14,851	)	$	388		$	(3,099	)
Net loss		-		-		-			-			(10,781	)		-			(10,781	)
Balance at June 30, 2025		2,405,146	$	-	$	(106	)	$	43,248		$	(39,882	)	$	269		$	3,529

	Shares		Amount		capital		deficit			income			deficit
	Common stock				Additional paid-in		Accumulated			Accumulated other comprehensive			Total stockholders’ equity
	Shares		Amount		capital		deficit			income			(deficit)

Balance at April 1, 2024		49,219	$	-	$	11,365	$	(14,851	)	$	388		$	(3,098	)
Issuance of Common Stock for services		64		-		150		-			-			150
Issuance of Common Stock upon vesting of restricted stock units		49		-		-		-			-			-
Issuance of Warrants		-		-		2,388		-			-			2,388
Stock-based compensation		-		-		482		-			-			482
Foreign currency translation adjustment		-		-		-		-			(1	)		(1	)
Net loss		-		-		-		(5,383	)		-			(5,383	)
Balance at June 30, 2024		49,332	$	-	$	14,385	$	(20,234	)	$	387		$	(5,462	)

	Common stock				Additional paid-in		Accumulated			Accumulated other comprehensive			Total stockholders’ equity
	Shares		Amount		capital		deficit			income			(deficit)

Balance at January 1, 2024		49,219	$	-	$	10,431	$	(11,299	)	$	411		$	(457	)
Balance		49,219	$	-	$	10,431	$	(11,299	)	$	411		$	(457	)
Issuance of Common Stock for services		64		-		150		-			-			150
Issuance of Common Stock upon vesting of restricted stock units		49		-		-		-			-			-
Issuance of Warrants		-		-		2,890		-			-			2,890
Stock-based compensation		-		-		914		-			-			914
Foreign currency translation adjustment		-		-		-		-			(24	)		(24	)
Net loss		-		-		-		(8,935	)		-			(8,935	)
Balance at June 30, 2024		49,332	$	-	$	14,385	$	(20,234	)	$	387		$	(5,462	)
Balance		49,332	$	-	$	14,385	$	(20,234	)	$	387		$	(5,462	)

The accompanying notes are an integral part of these condensed consolidated financial statements.

~~CONDUIT PHARMACEUTICALS~~CDT EQUITY INC.

CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS

(unaudited)

(in thousands)

	2025			2024
	Three Months ended March 31,
	Six Months ended June 30,
	2025			2024
Cash flows used in operating activities:
Net loss	$	(510,~~146~~781	)	$	(38,~~552~~935	)
Adjustments to reconcile net loss to net cash used in operating activities:
Loss on debt extinguishment, net		1,840			-
Gain on debt extinguishment, net		(278	)		-
Unrealized foreign exchange loss (gain)		(26	)		6
Unrealized foreign exchange loss		(27	)		5
Gain on debt extinguishment		(274	)		-
Loss on change in fair value of convertible notes payable		2,875			-
Gain on change in fair value of warrants		(130	)		(19	)
Gain on change in fair value of derivative warrant liability		(137	)		(110	)
Gain on waiver of accrued interest		(371	)		-
Operating lease obligations		29			(25	)
Non-cash lease expense		60			-
Issuance of warrants for lock-up		-			~~502~~2,710
Stock-based compensation expense		~~234~~394			~~431~~914
Non-cash interest expense		~~167~~224			79158
Depreciation expense		5			-
Operating lease obligations		-			(34	)
Amortization of financed Directors and Officers insurance		369			422
Depreciation expense		10			-
Amortization Expense		185			-
Amortization of financed directors and officers insurance		739			863
Issuance of common stock for services		-			150
Amortization expense		1,015			-
Changes in operating assets and liabilities:
Prepaid expenses and other current assets		~~(255~~198	)		(~~153~~306	)
Accounts payable		(~~721~~236	)		~~(97~~811	)
Accrued expenses and other liabilities		(~~207~~136	)		49(96	)
Lease liability		(2858	)		-
Net cash flows used in operating activities		(46,~~329~~509	)		(23,~~357~~870	)
Cash flows used in investing activities:
Purchases if property and equipment		(4	)		-
Purchases of equipment and clinical assets		(405	)		(10	)
Net cash flows used in investing activities		(4	)		-
Purchases of short-term investments		-			(490	)
Proceeds from the sale of short-term investments		-			276
Net cash flows used in investing activities		(405	)		(224	)
Cash flows provided by financing activities:
Proceeds from issuance of common shares related to ATM program		8,061			-
Proceeds from issuance of warrants from lock-up		-			113
Proceeds from issuance of common shares related to the ATM program		11,948			-
Repayment of notes payable – related parties		(425	)		-
Repayment of notes payable		(~~151~~156	)		-
Repayment of convertible notes payable - related parties		(927	)		-
Repayment of convertible notes payable – related parties		(927	)		-
Repayment of convertible notes payable		(~~631~~650	)		-
Net cash flows provided by financing activities		5,927			-
Purchases of treasury stock		(106	)		-
Net change in cash and cash equivalents before effect of exchange rate changes		1,594			(2,357	)
Net cash flows provided by financing activities		9,684			113
Effect of exchange rate changes on cash and cash equivalents		(18	)		(27	)
Net change in cash and cash equivalents before effect of exchange rate changes		2,770			(3,981	)
Net change in cash		1,576			(2,384	)
Effect of exchange rate changes on cash and cash equivalents		8			(28	)
Net change in cash		2,778			(4,009	)
Cash and cash equivalents at beginning of period		554			4,228
Cash and cash equivalents at end of period	$	23,~~130~~332		$	~~1,844~~219
Supplemental cash flow information:
Cash paid for interest	$	-		$	80
Non-cash investing and financing activities
Right of Use Asset obtained in exchange for Operating Lease Liabilities	$	-		$	350
Right-of-use assets obtained in exchange for operating lease liabilities	$	-		$	350
Issuance of Common Stock Upon Exercise of Conversion Option	$	4,077		$	-
Issuance of common stock upon exercise of conversion option		5,950			-
Supplemental Cash Disclosures
Issuance of common stock for services		2,951			-
Cash paid for interest	$	170		$	80
Purchases of PP&E in accounts payable		-			40
Receivables from issuance of warrants for lock-up		-			67

The accompanying notes are an integral part of these condensed consolidated financial statements.

~~CONDUIT PHARMACEUTICALS~~CDT EQUITY INC.

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

1. Nature of the Business, Basis of Presentation and Summary of Significant Accounting Policies

CDT Equity Inc., formerly Conduit Pharmaceuticals Inc., a Delaware corporation (“~~Conduit~~CDT” or the “Company”), is a ~~dynamic, multi~~ data-~~asset~~driven ~~clinical~~pharmaceutical ~~stage,~~development ~~life science~~ company ~~delivering~~ anfocused ~~efficient model for compound development. Conduit both acquires and funds the development of Phase 2-ready assets~~on identifying, ~~building an integrated and advanced platform-driven approach powered by artificial intelligence (AI) and cybernetics~~enhancing, and ~~seeking~~advancing ~~an exit through third~~high-~~party~~potential ~~license~~therapeutic ~~deals following successful clinical trials. Our novel approach addresses unmet medical needs and lengthens the intellectual property for our existing~~ assets through ~~cutting-edge~~scientific ~~solid-form~~innovation ~~technology~~and ~~with~~strategic ~~the expectation of commercializing these products with~~partnerships. ~~life~~The ~~science~~company ~~companies. Led~~has byevolved ainto ~~highly experienced team of executives including Dr. Andrew Regan and Dr. Freda Lewis-Hall, this novel approach is~~ a ~~departure from the traditional pharma/biotech business model of taking assets through regulatory approval. At this time~~broader, wemore doagile ~~not~~platform ~~expect~~ that weleverages ~~will~~artificial ~~commercialize~~intelligence, ~~any~~solid-form ~~clinical~~chemistry, ~~assets or seek marketing approval from the FDA (or similar organizations)~~and asefficient weasset ~~intend~~repositioning to ~~enter~~accelerate ~~into agreements with third parties for each such clinical asset that would provide that such third party would pursue~~ the ~~further~~ development, ~~commercialization, and marketing~~ of ~~such~~novel ~~assets~~treatments.

OnOur ~~September~~strategy ~~22,~~is ~~2023~~centered (on unlocking the ~~“Closing~~untapped ~~Date”),~~value aof ~~merger~~clinical-stage ~~transaction~~compounds, ~~between~~particularly ~~Conduit~~those ~~Pharmaceuticals~~deprioritized ~~Limited~~by ~~(“Old~~larger ~~Conduit”),~~pharmaceutical ~~Murphy~~companies ~~Canyon~~with ~~Acquisition~~strong, ~~Corp~~supporting ~~(“MURF”)~~Phase ~~and~~I ~~Conduit~~safety ~~Merger Sub, Inc~~data., aThrough ~~Cayman~~advanced ~~Islands~~co-crystallization ~~exempted company~~ and asolid-form ~~wholly~~technologies ~~owned subsidiary~~developed ofat ~~MURF (“Merger Sub”), was completed (the “Merger”) pursuant to the initial merger agreement dated~~our ~~November~~Cambridge 8facilities, ~~2022~~we ~~and~~improve ~~subsequent~~drug ~~amendments~~properties ~~to the merger agreement dated January 27, 2023~~ and ~~May~~extend ~~11,~~patent ~~2023~~life ~~(the~~by ~~“Merger~~up ~~Agreement”). Pursuant~~ to ~~the~~20 ~~terms~~years. ofIn ~~the~~partnership ~~Merger Agreement, on the Closing Date, (i) Merger Sub merged~~ with ~~and into Old Conduit~~Sarborg, ~~with~~we ~~Old~~also ~~Conduit~~apply ~~surviving the merger as a wholly~~AI-~~owned~~powered ~~subsidiary~~disease ofmapping ~~MURF, and (ii) MURF changed its name from Murphy Canyon Acquisition Corp.~~ to ~~Conduit Pharmaceuticals~~rapidly ~~Inc.~~identify ~~The~~new ~~common~~therapeutic ~~stock~~applications offor ~~the~~existing Company commenced trading on The Nasdaq Global Market under the symbol “CDT” on September 25, 2023, and the Company’s warrants commenced trading on The Nasdaq Capital Market under the symbol “CDTTW” on September 25, 2023compounds.

Our pipeline includes candidates that target autoimmune disorders, as well as idiopathic male infertility, oncology, dermatology, and animal health. Ongoing in vitro and in vivo studies, guided by AI insights, are designed to support licensing and commercialization partnerships, We will seek an exit through third-party license deals following successful in vitro and in vivo pre-clinical trials, entering into agreements with third-parties to pursue further development, FDA approval, commercialization and marketing of our assets.

Operating with a lean, asset-agnostic model, CDT Equity Inc. prioritizes speed, adaptability, and capital efficiency. We avoid the cost burden of late-stage clinical trials, focusing instead on high-leverage development strategies.

On September 22, 2023 (the “Closing Date”), a merger transaction between Conduit Pharmaceuticals Limited (“Old Conduit”), Murphy Canyon Acquisition Corp (“MURF”) and Conduit Merger Sub, Inc., a Cayman Islands exempted company and a wholly owned subsidiary of MURF (“Merger Sub”), was completed (the “Merger”) pursuant to the initial merger agreement dated November 8, 2022 and subsequent amendments to the merger agreement dated January 27, 2023 and May 11, 2023 (the “Merger Agreement”). Pursuant to the terms of the Merger Agreement, on the Closing Date, (i) Merger Sub merged with and into Old Conduit, with Old Conduit surviving the merger as a wholly-owned subsidiary of MURF, and (ii) MURF changed its name from Murphy Canyon Acquisition Corp. to Conduit Pharmaceuticals Inc. On September 25, 2023, the Company’s Common Stock commenced trading on The Nasdaq Capital Market under the symbol “CDT” and the Company’s warrants commenced trading on The Nasdaq Capital Market under the symbol “CDTTW”. Effective August 5, 2025, the Company changed its name from Conduit Pharmaceuticals Inc. to CDT Equity Inc. Our change to CDT Equity Inc. reflects the evolution of our strategy as a data-driven biotech development company focused on identifying, enhancing, and advancing high-potential therapeutic assets through scientific innovation and strategic partnerships.

Basis of Presentation

The accompanying unaudited condensed consolidated financial statements have been prepared by the Company in accordance with U.S. GAAP as set forth by the Financial Accounting Standards Board (“FASB”) and pursuant to the rules and regulations of the United States Securities and Exchange Commission (“SEC”). References to U.S. GAAP issued by the FASB in these notes to the accompanying unaudited condensed consolidated financial statements are to the FASB Accounting Standards Codifications (“ASC”) and Accounting Standards Update (“ASUs”).

The accompanying unaudited condensed consolidated financial statements and related notes have been prepared in accordance with U.S. GAAP for interim financial information, and with the rules and regulations of the SEC set forth in Article 8 of Regulation S-X. Accordingly, they do not include all of the information and footnotes required by U.S. GAAP for complete financial statements. The unaudited interim financial statements furnished reflect all adjustments (consisting of normal recurring accruals) which are, in the opinion of management, necessary to a fair statement of the results for the interim periods presented. Unaudited interim results are not necessarily indicative of the results for the full fiscal year. These condensed consolidated financial statements should be read along with our Annual Report on Form 10-K for the year ended December 31, 2024, filed with the SEC on March 28, 2025. The consolidated balance sheet as of December 31, 2024 was derived from the audited consolidated financial statements as of and for the year then ended.

The accompanying interim unaudited condensed consolidated financial statements included in this quarterly report have been prepared in accordance with U.S. GAAP and, in the opinion of the Company, contain all adjustments, consisting of only normal recurring adjustments, necessary for a fair statement of its financial position as of March 31, 2025, and its results of operations for the three months ended March 31, 2025 and 2024, and cash flows for the three months ended March 31, 2025 and March 31, 2024. The condensed consolidated balance sheet at December 31, 2024, was derived from the audited annual financial statements but does not contain all of the footnote disclosures from the annual financial statements.

Reclassifications

In certain instances, amounts reported in prior years’ consolidated financial statements have been reclassified to conform to the current presentation. Such reclassifications had no effect on previously reported stockholders’ equity (deficit) or net loss.

Principles of Consolidation

The accompanying unaudited condensed consolidated financial statements include the accounts of the Company and its wholly owned ~~subsidiaries~~ subsidiaries Conduit UK Management Ltd. (United Kingdom) and Conduit Pharmaceuticals, Ltd. (Cayman Islands). As used herein, references to the “Company” or “CDT” include references to ~~Conduit~~CDT ~~Pharmaceuticals~~Equity Inc. and its subsidiaries. All intercompany balances and transactions have been eliminated in consolidation.

Liquidity and Going Concern

In accordance with ~~Accounting Standards Codification (“~~ASC”) 205-40, Going Concern, the Company has evaluated whether there are conditions and events, considered in the aggregate, that raise substantial doubt about the Company’s ability to continue as a going concern within one year after the date the financial statements are issued. Since its inception, the Company has generated significant losses and as of ~~March~~June 3130, 2025, the Company had an accumulated deficit of $3439.2 9 million. As of ~~March~~June 3130, 2025 and December 31, 2024, the Company had cash and cash equivalents of $23.13 million and $0.6 million, respectively. For the ~~three~~six months ended ~~March~~June 3130, 2025 and 2024, the Company had net losses of $510.1 8 million and $38.6 9 million, respectively, and cash used in operating ~~activities~~ activities of $46.3 5 million and $23.4 9 million, respectively.

Management has determined that it does not have sufficient cash and other sources of liquidity to fund its current business plan. These factors raise substantial doubt regarding the Company’s ability to continue as a going concern for at least the next 12 months from the financial statement filing date.

The Company’s expectation is to generate operating losses and negative operating cash flows in the future and will need additional funding to support its current business plan in addition to the remaining at the market offering program (the “Sales Agreement”) of approximately $128.0 2 million (see Note 109), as of the financial statement issuance date. Management’s plans to alleviate the conditions that raise substantial doubt through the pursuit of additional cash resources through public or private equity or debt financings. However, there is no assurance that such funding will be available when needed or on acceptable terms. If additional funding is not available when required, the Company would need to delay or curtail its operations and its research and development activities until such ~~funding~~ funding is received, all of which could have a material adverse effect on the Company and its financial condition.

These financial statements have been prepared assuming the Company will continue as a going concern and do not include adjustments to reflect the possible effects on the recoverability and classification of assets or the amounts and classification of liabilities that may result from the outcome of this uncertainty.

Reverse Stock Split

On January 24, 2025, the Company amended its Second Amended and Restated Certificate of Incorporation with the Secretary of State of the State of Delaware in order to effect a 1-for-100 reverse stock split of its outstanding shares of ~~common~~Common ~~stock~~Stock (the “~~Reverse~~January ~~Stock~~Reverse Stock Split”). As a result of the reverse stock split, every 100 shares of the Company’s ~~common~~Common ~~stock~~Stock issued or outstanding ~~were~~ were automatically reclassified into one new share of ~~common~~Common ~~stock~~Stock, subject to the treatment of fractional shares as described below, ~~without~~ without any action on the part of the holders. ~~All~~The ~~historical~~January share and per-share amounts reflected throughout the accompanying consolidated financial statements and other financial information in this Quarterly Report on Form 10-Q have been retroactively adjusted to reflect the 2025 Reverse Stock Split ~~as if the split occurred as of the earliest period presented. The Reverse Stock Split~~ did not affect the number of authorized shares of ~~common~~Common ~~stock~~Stock or the par value of the ~~common~~Common ~~stock~~Stock. No fractional shares were issued in connection with the January Reverse Stock Split. Stockholders who would otherwise have been entitled to receive fractional shares as a result of the January Reverse Stock Split were entitled to a cash payment in lieu thereof at a price equal to the fraction to which the stockholder would otherwise be entitled multiplied by the closing price per share of the ~~common~~Common ~~stock~~Stock (as adjusted to give effect to the January Reverse Stock Split) on The Nasdaq Global Market on January 24, 2025.

Other Risks and Uncertainties

The Company is subject to risks common to companies in the development stage and pharmaceutical industry including, but not limited to, uncertainties related to pre-clinical and clinical outcomes competitor products, regulatory approvals, dependence on key products, dependence on key suppliers and protection of intellectual property rights (see Note 15 for details on a claim against our AZD 1656 co-crystal patent). Clinical assets currently under development will require significant additional research and development efforts, including extensive preclinical and clinical testing and regulatory approval prior to commercialization. These efforts will require significant amounts of additional capital, adequate personnel, infrastructure, and extensive compliance and reporting capabilities. Even if the Company’s efforts are successful, it is uncertain when, if ever, the Company will realize significant revenue and cash flow from royalties or product sales.

The Company licenses clinical assets from AstraZeneca. See Note 7. If there is a breach or other termination of such agreements, there could be a material adverse effect on the Company’s business, financial condition, operating results, and prospects.

The Company is also subject to risks associated with the Nasdaq Stock Market (“Nasdaq”) correspondence and subsequent Nasdaq Capital Market Listing application.

In August 2024, the Company received deficiency letters from Nasdaq notifying the Company that it was not in compliance with Listing Rule 5450(a)(1) (the “Bid Price Rule”), Listing Rule 5450(b)(2)(C) (the “MVPHS Rule”) and Listing Rule 5450(b)(2)(A) (the “MVLS Rule”, together with the Bid Price Rule and the MVPHS Rule, the “Rules”). The Company had until February 10, 2025, and February 11, 2025, to regain compliance with the Rules. On December 17, 2024, Nasdaq issued a letter to the Company that as of December 17, 2024, it determined that the Company’s securities had a closing bid price of $0.10 or less for ten consecutive trading days. As a result, Nasdaq had determined to delist the Company’s common stock and redeemable warrants from The Nasdaq Global Market, on December 27, 2024. The Company subsequently requested and received a hearing (the “Nasdaq Hearing”) from the Nasdaq Hearings Panel (the “Panel”). The Company submitted a written plan of compliance to cure its Rule deficiencies to Nasdaq on January 22, 2025, and attended the Nasdaq Hearing for the Company on February 11, 2025. On March 5, 2025, the Company received a written notification (the “Notice”) from the Panel confirming it has granted the Company such an extension for the Company to regain compliance with the MVPHS and MVLS rules, provided that the Company, (i) on or before March 12, 2025, files an application to transfer to the Nasdaq Capital Market, which application was submitted on March 7, 2025, and (ii) on or before March 31, 2025, demonstrates compliance with all Nasdaq listing rules, which the Company believe it has. To date, the Company has not been notified by Nasdaq whether its application to transfer to the Nasdaq Capital has been accepted and the Company continues to trade on the Nasdaq Global Market. Additionally, the Company was also notified in the Notice that as of February 26, 2025, it had regained compliance with the Bid Price Rule. There is no guarantee that the Company can maintain ongoing compliance with the Bid Price Rule.

On May 15, 2025, the Company amended its Second Amended and Restated Certificate of Incorporation with the Secretary of State of the State of Delaware to effectuate a 1-for-15 reverse stock split of the outstanding shares of the Company’s Common Stock (the “May Reverse Stock Split”). At the Company’s Special Meeting of Stockholders on May 5, 2025, stockholders approved the reverse stock split and granted the Company’s Board of Directors (the “Board”) the authority to determine the exact split ratio and when to proceed with the reverse stock split. The May Reverse Stock Split became effective on May 19, 2025, at 5:00 p.m., Eastern Time (the “Effective Time”) and the Common Stock began trading on The Nasdaq Global Market on a May Reverse Stock Split-adjusted basis on May 20, 2025, at market open under the existing ticker symbol, “CDT.” As of the Effective Time, every 15 shares of the Company’s issued and outstanding Common Stock was combined into one share of Common Stock. The May Reverse Stock Split did not affect the number of authorized shares of Common Stock or the par value of the Common Stock. No fractional shares were issued in connection with the May Reverse Stock Split. Stockholders who would otherwise have been entitled to receive fractional shares as a result of the May Reverse Stock Split were entitled to a cash payment in lieu thereof at a price equal to the fraction to which the stockholder would otherwise be entitled multiplied by the closing price per share of the Common Stock (as adjusted to give effect to the May Reverse Stock Split) on The Nasdaq Global Market on May 20, 2025.

All historical share and per-share amounts reflected throughout the accompanying consolidated financial statements and other financial information in this Quarterly Report on Form 10-Q have been retroactively adjusted to reflect the January Reverse Stock Split and May Reverse Stock Split as if the splits occurred as of the earliest period presented.

Other Risks and Uncertainties

The Company is subject to risks common to companies in the development stage and pharmaceutical industry including, but not limited to, uncertainties related to pre-clinical and clinical outcomes competitor products, regulatory approvals, dependence on key products, dependence on key suppliers and protection of intellectual property rights (see Note 14 for details on a claim against our AZD 1656 co-crystal patent). Clinical assets currently under development will require significant additional research and development efforts, including extensive preclinical and clinical testing and regulatory approval prior to commercialization. These efforts will require significant amounts of additional capital, adequate personnel, infrastructure, and extensive compliance and reporting capabilities. Even if the Company’s efforts are successful, it is uncertain when, if ever, the Company will realize significant revenue and cash flow from royalties or product sales.

The Company licenses clinical assets from AstraZeneca (see Note 6 for further detail). If there is a breach or other termination of such agreements, there could be a material adverse effect on the Company’s business, financial condition, operating results, and prospects.

Related party transactions and arrangements, specifically research and development related transactions, the Company enters into subject the Company to certain risks. Related party transactions in general are regarded as increasing the risk of omissions or misstatements in financial reporting, the risk of transactions being done on other than arm’s length terms due to the close ties between the parties involved and the risk of regulatory non-compliance. In addition, related-party transactions present potential conflicts of interest that could result in decisions that prioritize the economic interests of certain individuals over those of the primary purpose of the research and development, our company and its stockholders. In the instance of a dispute under any related-party agreement, the interests of affiliated parties may not align with the Company’s interest, and the resolution of such disputes may be less favorable than what the Company might achieve in a transaction with an unaffiliated third party.

The Company is also subject to risks associated with the Nasdaq Stock Market (“Nasdaq”) correspondence.

In August 2024, the Company received deficiency letters from Nasdaq notifying the Company that it was not in compliance with Listing Rule 5450(a)(1) (the “Bid Price Rule”), Listing Rule 5450(b)(2)(C) (the “MVPHS Rule”) and Listing Rule 5450(b)(2)(A) (the “MVLS Rule”, together with the Bid Price Rule and the MVPHS Rule, the “Rules”). The Company had until February 10, 2025, and February 11, 2025, to regain compliance with the Rules. On December 17, 2024, Nasdaq issued a letter to the Company that as of December 17, 2024, it determined that the Company’s securities had a closing bid price of $0.10 or less for ten consecutive trading days. As a result, Nasdaq had determined to delist the Company’s Common Stock and redeemable warrants from The Nasdaq Global Market, on December 27, 2024. The Company subsequently requested and received a hearing (the “Nasdaq Hearing”) from the Nasdaq Hearings Panel (the “Panel”). The Company submitted a written plan of compliance to cure its Rule deficiencies to Nasdaq on January 22, 2025, and attended the Nasdaq Hearing for the Company on February 11, 2025. On March 5, 2025, the Company received a written notification (the “Notice”) from the Panel confirming it had granted the Company an extension to regain compliance with the MVPHS and MVLS rules, provided that the Company, (i) on or before March 12, 2025, files an application to transfer to The Nasdaq Capital Market, which application was submitted on March 7, 2025, and (ii) on or before March 31, 2025, demonstrates compliance with all Nasdaq listing rules. The Company was notified in the Notice that as of February 26, 2025, it had regained compliance with the Bid Price Rule. There is no guarantee that the Company can maintain ongoing compliance with the Bid Price Rule. On May 15, 2025, the Company received formal notice from Nasdaq that the Company has regained compliance with Nasdaq’s minimum bid price requirement (the “Bid Price Requirement”) set forth in Nasdaq Listing Rule 5550(a)(2), as well as Nasdaq’s stockholders’ equity requirement (“Equity Requirement”) set forth in Nasdaq Listing Rule 5550(b)(1). On May 21, 2025, the Company received formal notice from Nasdaq that the Company’s application to transfer the listing of its Common Stock to The Nasdaq Capital Market had been approved and the Company’s securities were transferred to The Nasdaq Capital Market at the opening of business on May 23, 2025.

Summary of Significant Accounting Policies

Use of Estimates

The preparation of financial statements in conformity with U.S. GAAP requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities and related disclosures of contingent assets and liabilities at the date of the financial statements as well as the reported amounts of revenues and expenses during the reporting period. Estimates are based on several factors including the facts and circumstances available at the time the estimates are made, historical experience, risk of loss, general economic conditions and trends, and the assessment of the probable future outcome. Actual results could differ materially from such estimates. Estimates and assumptions are reviewed periodically by management and changes in estimates are made as management becomes aware of changes in circumstances surrounding the estimates. The effects of changes are reflected in the financial statements in the period that they are determined.

Cash and Cash Equivalents

Cash and cash equivalents are primarily maintained with major financial institutions in the United States and the United Kingdom. The Company considers cash equivalents to be short-term, highly liquid investments that (a) are readily convertible into known amounts of cash, (b) are traded and held for cash management purposes, and (c) have original maturities of three months or less at the time of purchase. The UK bank account, with a ~~year-end~~ balance at June 30, 2025 of approximately £~~206~~270,000 (or approximately $~~266~~370,000) exceeds the country’s deposit limit of £85,000 (approximately $110,000). The Company’s US depository bank participates in the Demand Deposit Marketplace program, insuring deposits up to $10 million by sweeping amounts in excess of the $250,000 deposit insurance limit among participating banks. The Company has not experienced any losses on any accounts through the ~~three~~ six months ended ~~March~~June 3130, 2025.

The Company had $23.13 million and $0.6 million in cash and cash equivalents on hand as of ~~March~~June 3130, 2025 and December 31, 2024, respectively. As of ~~March~~June 3130, 2025, $~~4,000~~ 0.3 million of the Company’s $23.13 million cash and cash equivalents balance was invested in money market funds. The money market funds do not have significant liquidity restrictions that would require the exclusion from cash and cash equivalents .

Fair Value Measurements

ASC Topic 820, Fair Value Measurements and Disclosures, defines fair value, establishes a framework for measuring fair value, and expands disclosures about fair value measurements. Fair value is to be determined based on the exchange price that would be received for an asset or paid to transfer a liability (an exit price) in the principal or most advantageous market for the asset or liability in an orderly transaction between market participants. In determining fair value, the Company used various valuation approaches. A fair value hierarchy has been established for inputs used in measuring fair value that maximizes the use of observable inputs and minimizes the use of unobservable inputs by requiring that the most observable inputs be used when available. Observable inputs are those that market participants would use in pricing the asset or liability based on market data obtained from sources independent of the Company.

Unobservable inputs reflect the Company’s assumption about the inputs that market participants would use in pricing the asset or liability developed based on the best information available in the circumstances. The fair value hierarchy is categorized into three levels, based on the inputs, as follows:

7● Level 1-Valuations based on quoted prices for identical instruments in active markets. Since valuations are based on quoted prices that are readily and regularly available in an active market, valuation of these instruments does not entail a significant degree of judgment. ● Level 2-Valuations based on observable inputs other than quoted prices included in Level 1, such as quoted prices for either similar instruments in active markets, identical or similar instruments in markets that are not active, or model-derived valuations whose inputs or significant value drivers are observable or can be corroborated by observable market data. ● Level 3-Valuations based on inputs that are unobservable. These valuations require significant judgment.

● Level 1-Valuations based on quoted prices for identical instruments in active markets. Since valuations are based on quoted prices that are readily and regularly available in an active market, valuation of these instruments does not entail a significant degree of judgment. ● Level 2- Valuations based on observable inputs other than quoted prices included in Level 1, such as quoted prices for either similar instruments in active markets, identical or similar instruments in markets that are not active, or model-derived valuations whose inputs or significant value drivers are observable or can be corroborated by observable market data. ● Level 3-Valuations based on inputs that are unobservable. These valuations require significant judgment.8

The Company’s Level 1 assets consist of cash and cash equivalents in the accompanying balance sheets, convertible notes payable and the value of accrued expenses and other current liabilities approximate fair value due to the short-term nature of these assets and liabilities.

As of ~~March~~June 3130, 2025, the Company has two financial liabilities, warrant liabilities for which the fair value is determined based on Level 2 and Level 3 inputs, and convertible debt carried at fair value for which the fair value is determined based on Level 3 input. The Level 2 inputs are valued based on observable inputs other than quoted prices included in Level 1, such as quoted prices for similar instruments in active markets. The ~~level~~Level 3 inputs as such inputs are based on unobservable inputs and require significant judgement.

Fair Value Option

The Company has elected the fair value measurement option for convertible debt with embedded derivatives that would otherwise require bifurcation and has recorded the entire hybrid financial instrument at fair value under the guidance in ASC 825, Financial Instruments. As a result, the August 2024 Nirland Note was recorded at fair value subsequent to the Second Amendment and the A.G.P. Convertible Note was recorded at fair value upon issuance. The notes will subsequently be remeasured at fair value each reporting date until settled or converted. The Company reports interest expense, including accrued interest, related to the convertible debt under the fair value option, separately from within the change in fair value of the convertible debt in the accompanying condensed consolidated statement of operations and comprehensive loss. Any changes in fair value caused by instrument-specific credit risk are presented separately in other comprehensive income.

Research and Development

Research and development expenses consist primarily of costs incurred in connection with the research and development of our clinical assets and programs, see Note 76 for further discussion of research and development expense. ~~Conduit~~CDT ~~holds~~licenses ~~all~~its ~~licenses~~assets tofrom ~~conduct~~a large pharmaceutical company and conducts clinical research ~~through~~ awith third-party ~~pharmaceutical~~contract research ~~company~~organizations. The Company expenses research and development costs and intangible assets acquired that have no alternative future use as incurred. These expenses include:

	●	expenses incurred under agreements with organizations that support the Company’s drug discovery and development activities;
	●	expenses incurred in connection with the preclinical and clinical development of the Company’s clinical assets and programs, including under agreements with contract research organizations, or CROs;
	●	costs related to contract manufacturing organizations, or CMOs, that are primarily engaged to provide drug substance and product for our clinical trials, research and development programs, as well as investigative sites and consultants that conduct the Company’s clinical trials, nonclinical studies and other scientific development services;
	●	the costs of acquiring and manufacturing nonclinical and clinical trial materials, including manufacturing registration and validation batches;
	●	employee-related expenses, including salaries, related benefits and equity-based compensation expense, for employees engaged in research and development functions;
	●	acquisition costs related to the purchase of licensed intellectual property;
	●	costs related to compliance with quality and regulatory requirements;
	●	payments made under third-party licensing agreements; and
	●	direct and allocated costs related to facilities, information technology, personnel and other overhead.

Advance payments that we make for goods or services to be received in the future for use in research and development activities are recorded as prepaid expenses. Such amounts are recognized as an expense as the goods are delivered or consumed or the related services are performed, or until it is no longer expected that the goods will be delivered, or the services rendered.

8Purchased Research and Development Assets

The Company accounts for its research and development costs in accordance with ASC 730, Research and Development. ASC 730 requires that research and development are generally recognized as an expense as incurred. However, some costs associated with research and development activities that have an alternative future use may be capitalizable. Purchases of assets related to research and development activities are evaluated based on the usefulness to the Company currently and for alternative future uses. Purchased research and development assets with alternative future use are recorded at cost and subsequently amortized using the straight-line method over their estimated useful lives. To date, the Company has one purchased asset, a diagnostic tool used to monitor clinical trials, aggregate data on an ongoing basis and tracking intellectual property patent status. The Company determined that the diagnostic tool also has the alternative future use of utilizing the predictive modeling capability to track and evaluate delisted patents in the marketplace to potentially facilitate strategic entry into de-prioritized asset markets that might be otherwise overlooked by other market participants. The asset is depreciated on a straight-line basis over its useful life of two years.

Income Taxes

ASC Topic 740, Income Taxes, sets forth standards for financial presentation and disclosure of income tax liabilities and expense. Interest and penalties recognized have been classified in the unaudited condensed consolidated statements of operations and comprehensive loss as income taxes. Deferred tax assets and liabilities are recognized for future tax consequences attributable to temporary differences between the financial statement carrying amount of existing assets and liabilities and their respective tax bases and operating losses carried forward. Deferred tax assets and liabilities are measured using enacted tax rates expected to apply to taxable income in the years in which those temporary differences are expected to be recovered or settled. The effect on deferred tax assets and liabilities of a change in tax rates is recognized in the unaudited condensed consolidated statements of operations and comprehensive loss in the period that includes the enactment date. The measurement of deferred tax assets is reduced, if necessary, by a valuation allowance for any tax benefits of which future realization is uncertain.

~~Earnings/(~~Net Loss) per Share Attributable to Common Stockholders

The Company calculates basic and diluted ~~earnings/(~~net loss) per share under ASC Topic 260, Earnings Per Share. Basic ~~earnings/(~~net loss) per share is computed by dividing the net ~~income/(~~loss) by the number of weighted-average common shares outstanding for the period. Diluted ~~earnings/(~~net loss) is computed by adjusting net ~~income/(~~loss) based on the impact of any dilutive instruments. Diluted ~~earnings/(~~net loss) per share is computed by dividing the diluted net ~~income/(~~loss) by the number of weighted-average common shares outstanding for the period including the effect, if dilutive, of any instruments that can be settled in common shares. When computing diluted net ~~income/(~~loss) per share, the numerator is adjusted to eliminate the effects that have been recorded in net ~~income/(~~loss) (net of tax, if any) attributable to any liability-classified dilutive instruments.

Warrants

The Company determines the accounting classification of Warrants as either liability or equity by first assessing whether the Warrants meet liability classification in accordance with ASC Topic 480, Distinguishing Liabilities from Equity (“ASC 480”). Under ASC 480, a financial instrument that embodies an unconditional obligation, or a financial instrument other than an outstanding share that embodies a conditional obligation, that the issuer must or may settle by issuing a variable number of its equity shares must be classified as a liability (or an asset in some circumstances) if, at inception, the monetary value of the obligation is based solely or predominantly on any one of the following: (a) a fixed monetary amount known at inception; (b) variations in something other than the fair value of the issuer’s equity shares; or (c) variations inversely related to changes in the fair value of the issuer’s equity shares.

If financial instruments, such as the Warrants, are not required to be classified as liabilities under ASC 480, the Company assesses whether such instruments are indexed to the Company’s own stock under ASC 815-40. In order for an instrument to be considered indexed to an entity’s own stock, its settlement amount must always equal the difference between the following: (a) the fair value of a fixed number of the Company’s equity shares, and (b) a fixed monetary amount or a fixed amount of a debt instrument issued by the Company. The Company determined that the settlement amount of the Equity Classified Warrants would equal the difference between the fair value of a fixed number of shares and a fixed monetary amount (or a fixed amount of a debt instrument) and must be classified as equity, while the settlement amount of the Liability Classified Warrants would not equal the difference between the fair value of a fixed number of shares and a fixed monetary amount (or a fixed amount of a debt instrument) and must be classified as a liability.

The Equity Classified Warrants are recorded in stockholders’ equity (deficit) and the Liability Classified Warrants are recorded as liabilities in the Condensed Consolidated Balance Sheet. The Liability Classified Warrants are remeasured each period with changes in fair value recorded in the Condensed Consolidated Statements of Operations and Comprehensive Loss.

910

Foreign Currency Translation

The Company translated the assets and liabilities of foreign subsidiaries from their respective functional currency, the British pound, to United States dollars at the appropriate spot rates as of the balance sheet date. Income and expenses of operations are translated to United States dollars using weighted average exchange rates during the year. The foreign subsidiaries use the local currency as their functional currency. The effects of foreign currency translation adjustments are included as a component of accumulated other comprehensive income in the accompanying consolidated statements of changes in stockholders’ equity (deficit). Non-monetary items in the subsidiaries’ functional currency are re-measured into the reporting currency at the historical exchange rate (i.e., the rate of exchange at the date of the transaction).

Recently Issued Accounting Standards Not Yet Adopted

In December 2023, the FASB issued ASU 2023-09, Income Taxes (Topic 740): Improvements to Income Tax Disclosures (“ASU 2023-09”). ASU 2023-09 modifies the reporting requirements for income tax disclosures related to effective tax rates and cash income taxes paid. Pursuant to ASU 2023-09, public business entities are required to disclose certain categories in the income tax rate reconciliation, as well as additional information for reconciling items that meet a specific quantitative threshold. Additionally, ASU 2023-09 requires annual disclosures of income taxes paid for all entities, including the amount of income taxes paid, net of refunds received, disaggregated by federal, state, and foreign jurisdictions. ASU 2023-09 is effective for the Company in its annual reporting for fiscal 2025 on a prospective basis. Early adoption and retrospective reporting are permitted. The Company does not plan to adopt this standard early. The Company is currently evaluating the impact of ASU 2023-09 on its consolidated financial statements.

In November 2024, the FASB issued ASU 2024-03, Income Statement-Reporting Comprehensive Income-Expense Disaggregation Disclosures (Subtopic 220-40): Disaggregation of Income Statement Expenses, which is intended to provide more detailed information about specified categories of expenses (purchases of inventory, employee compensation, depreciation and amortization) included in certain expense captions presented on the consolidated statements of operations and comprehensive income (loss). The guidance in this ASU is effective for fiscal years beginning after December 15, 2026, and interim periods within fiscal years beginning after December 15, 2027. Early adoption is permitted. The amendments may be applied either (1) prospectively to financial statements issued for periods after the effective date of this ASU or (2) retrospectively to all prior periods presented in the consolidated financial statements. The Company is currently evaluating the impact that the adoption of ASU 2024-03 will have on its consolidated financial statements and disclosures.

2. Fair Value

~~During the period ended March 31, 2025, there were no transfers between Level 1 and Level 2, nor into or out of Level 3.~~ The following table presents as of ~~March~~June 3130, 2025 the Company’s assets and liabilities subject to measurement at fair value on a recurring basis (in thousands):

	Fair Value Measurements as of March 31, 2025
	Fair Value Measurements as of June 30, 2025
	Level 1		Level 2		Level 3		Total
Assets:
Cash equivalents	$	4331	$	-	$	-	$	4331
Total Assets	$	4331	$	-	$	-	$	4331
Liabilities:
Convertible note payable, at fair value	$	-	$	-	$	2,663	$	2,663
Convertible notes payable, at fair value	$	-	$	-	$	1,882	$	1,882
Liability Classified Warrants		-		-		81		81
Total Liabilities	$	-	$	-	$	21,~~671~~883	$	21,~~671~~883

~~The following table presents as of December 31, 2024 the Company’s liabilities subject to measurement at fair value on a recurring basis (in thousands):~~11

The following table presents as of December 31, 2024 the Company’s assets and liabilities subject to measurement at fair value on a recurring basis (in thousands):

	Fair Value Measurements as of December 31, 2024
	Level 1		Level 2		Level 3		Total
Assets:
Cash equivalents	$	192	$	-	$	-	$	192
Total Assets	$	192	$	-	$	-	$	192

Liabilities:
Convertible notes payable, at fair value	$	-	$	-	$	5,856	$	5,856
Liability Classified Warrants		-		-		138		138
Total Liabilities	$	-	$	-	$	5,994	$	5,994

Cash equivalents consist of highly liquid money market funds with maturities of three months or less and are reflected in the Condensed consolidated balance sheets at carrying value, which approximates fair value due to their short-term nature.

The following table presents additional information about the Convertible Notes Payable subject to measurement at fair value on a recurring basis and warrant liabilities, for which the Company used significant unobservable inputs (Level 3) (in thousands):

	Convertible Notes Payable			Liability Classified Warrants
Balance as of December 31, 2024	$	5,856		$	138
Repayment of convertible note		(1,054	)		-
Repayment of convertible notes		(1,054	)		-
Change in fair value		(2,139	)		(131	)
Balance as of March 31, 2025	$	2,663		$	7
Beginning balance	$	2,663		$	7
Conversion of convertible notes		(1,872	)		-
Interest expense		57			-
Change in fair value		1,034			(6	)
Balance as of June 30, 2025	$	1,882		$	1
Ending balance	$	1,882		$	1

10During the three and six months ended June 30, 2025, there were no transfers between Level 1 and Level 2, nor into or out of Level 3.

Convertible Notes Payable

As discussed in Note 4, on October 31, 2024, the Company and Nirland agreed to amend the Senior Secured Promissory Note entered into by the Company and Nirland on August 6, 2024 (the “August 2024 Nirland Note”), whereby the August 2024 Nirland Note was amended to provide for the conversion of the August 2024 Nirland Note into shares of ~~common~~Common ~~stock~~Stock, at Nirland’s discretion, in a multiple of any unpaid amounts, if not otherwise previously paid, pursuant to the conversion rate contained therein. The August 2024 Nirland Note was then amended for a second time on November 22, 2024. On February 12, 2025, the August 2024 Nirland Note was repaid in full.

Additionally, as discussed in Note 4, during November 2024, the Company issued to A.G.P./Alliance Global Partners (“A.G.P.”) a convertible promissory note (the “A.G.P. Convertible Note”) in the principal amount of $5.7 million to evidence the A.G.P.’s currently owed deferred commission payable.

The Company elected to account for the August 2024 Nirland Note and A.G.P. Convertible Note (collectively the “Convertible Notes Payable”) at fair value. The fair value of the Convertible Notes Payable is estimated each period using a binomial lattice model. Significant estimates in the binomial lattice model include the Company’s stock price, volatility, risk-free rate, corporate bond yield, credit spread, probability of default, and recovery upon default.

As of ~~March~~June 3130, 2025, no obligations remain under the August 2024 Nirland Note (refer to Note 4 for details) and therefore only the fair value of the A.G.P. Convertible Note was estimated using a binomial lattice model.

~~The following table outlines the range of significant unobservable inputs used in calculating the fair value of the A.G.P. Convertible Note as of March 31, 2025, and December 31, 2024:~~12

The following table outlines the range of significant unobservable inputs used in calculating the fair value of the A.G.P. Convertible Note as of June 30, 2025, and December 31, 2024:

Schedule of Fair Value of Assumptions

	March 31, 2025			December 31, 2024
	June 30, 2025			December 31, 2024
Stock Price	$	02.7876		$	6103.9050
Term (years)		0.6541			0.9
Corporate bond yield		1116.13	%		9.0	%
Credit Spread		26.2	%		26.2	%
Probability of Default		40	%		40	%
Recovery upon default		0	%		0	%
Volatility		~~167~~194.03	%		101.6	%

Liability Classified Warrants

The A.G.P. 2024 Warrants, as defined in Note 1413, are accounted for as liabilities in accordance with ASC 815-40 and are presented within Warrant liabilities in the condensed consolidated balance sheets. Warrant liabilities are measured at fair value at inception and on a recurring basis, with changes in fair value presented within other income (expense), net in the condensed consolidated statements of operations and comprehensive loss.

11The measurement of the A.G.P. 2024 Warrants is classified as Level 3 due to the use of an option-pricing model that utilizes unobservable inputs and requires significant judgement. The Company estimated the fair value of the A.G.P. 2024 Warrants as of June 30, 2025 and December 31, 2024, utilizing a Black-Scholes option-pricing model with the following assumptions:

The measurement of the A.G.P. 2024 Warrants is classified as Level 3 due to the use of an option-pricing model that utilizes unobservable inputs and requires significant judgement. The Company estimated the fair value of the A.G.P. 2024 Warrants as of March 31, 2025 and December 31, 2024, utilizing a Black-Scholes option-pricing model with the following assumptions:

Schedule of Fair Value of Assumptions

	March 31, 2025			December 31, 2024
	June 30, 2025			December 31, 2024
Closing stock price	$	02.7876		$	6103.9050
Contractual exercise price	$	10157.4820		$	10157.4820
Risk-free rate		43.7879	%		4.38	%
Estimated volatility		9795.05	%		98.6	%
Time period to expiration (in years)		4.7853			5.0

3. Balance Sheet Details

Prepaid expenses and other current assets consisted of the following as of ~~March~~June 3130, 2025 and December 31, 2024 (in thousands):

Schedule of Balance Sheet Details

	As of		As of
	As of June 30, 2025		As of December 31, 2024
	March 31, 2025		December 31, 2024
Prepaid directors’ and officers’ insurance	$	606	$	1,187
Prepaid directors’ and officers’ insurance	$	897	$	1,187
Prepaid expenses		437		85
Prepaid expenses		341		85
Prepaid expenses – related parties		-		20
Prepaid expenses		-		20
Other receivables		~~488~~245		489
Total prepaid expenses and other current assets	$	1,~~726~~288	$	1,781

~~Accrued Expenses and other current liabilities consisted of the following as of March 31, 2025 and December 31, 2024 (in thousands):~~13

Accrued expenses and other current liabilities consisted of the following as of June 30, 2025 and December 31, 2024 (in thousands):

	As of		As of
	As of June 30, 2025		As of December 31, 2024
	March 31, 2025		December 31, 2024
Accrued professional fees	$	334	$	242
Accrued professional fees	$	546	$	242
Accrued board of director fees		-		101
Accrued research & development costs		16248		280
Accrued payroll		89		51
Accrued legal contingency		~~402~~426		389
Accrued interest		-		383
Accrued commission payable		-		107
HMRC payable		5863		396
Other		1560		14
Total accrued expenses and other current liabilities	$	1,~~045~~140	$	1,963

4. Convertible Notes Payable

Convertible Promissory ~~Notes~~Note Payable

During March 2023, the Company issued a convertible promissory note payable (the “Convertible Promissory ~~Notes~~Note Payable”) with an aggregate principal amount of $0.8 million to a non-related third party. The Convertible Promissory Note Payable had a maturity date of 18 months from the date of issuance. ~~The~~and ~~note~~ carries interest at a rate of 20% annually, which is payable every six (6) months from the date of the note until the maturity date.

On March 6, 2025, the Company reached a Settlement Agreement (the “Settlement Agreement”) with the loan holder to pay $0.7 ~~million~~ million in order to settle the ~~March 2023~~ Convertible Promissory Note Payable in full. The Company repaid the loan holder the settlement amount of $0.7 million on March 13, 2025. The Settlement Agreement and subsequent repayment was treated as a debt extinguishment under ASC 470-50. During the three and six months ended ~~March~~June 3130, 2025, the Company recorded a gain on debt extinguishment of $0.1 million, calculated as the difference between (i) the $0.8 million carrying value of the Convertible Promissory Note Payable immediately prior to the amendment, and (ii) the $0.7 million repayment of the ~~March 2023~~ Convertible Promissory Note Payable. The $0.1 million gain on debt extinguishment was recorded within other income (expense) in the condensed consolidated statement of operations and comprehensive loss for the ~~three~~six months ended ~~March~~June 3130, 2025.

In connection with the Settlement Agreement, the Company entered into a consulting agreement with a third party to negotiate the settlement of the ~~convertible~~Convertible ~~note~~Promissory Note Payable with the loan holder on behalf of the Company. In exchange for negotiating the Settlement Agreement, the Company agreed to pay $0.1 million through the issuance of shares of Common Stock or cash. On March 31, 2025, the Company issued 734,~~074~~872 shares of Common Stock. The number of shares issued was determined based on the agreement amount of $0.1 million, divided by the closing share price on March 28, 2025 (prior trading date) of $013.8935. The $0.1 million was recorded as interest expense in the condensed consolidated statement of operations and comprehensive income loss for the ~~three~~six months ended ~~March~~June 3130, 2025.

For the three months ended ~~March~~June 3130, 2025 and 2024, the Company incurred interest expense on the Convertible Promissory Note Payable of zero and ~~March~~$40,000, 31respectively. For the six months ended June 30, 2025 and 2024, the Company incurred interest expense on the Convertible Promissory Note Payable of $0.1 million and $400.1 million,~~000,~~ respectively.

August 2024 Nirland Note

On August 6, 2024, the Company entered into August 2024 Nirland Note with Nirland Limited (“Nirland”), a related party of the Company, pursuant to which the Company issued and sold to Nirland the August 2024 Note in the original principal amount of $2.7 million, inclusive of a $0.5 million original issuance discount. See Note 1110 for further reference to the relationship between the Company and Nirland. Of the total amount of the August 2024 Nirland Note, $1.7 million was issued upon execution of the August 2024 Nirland Note. The balance of $0.5 million was provided to the Company when the shares were registered for resale in September 2024. In the event the Company completes any public or private equity or debt financing, the Company shall be required to mandatorily prepay (“Mandatory Prepayment Right”), any amounts that may be then outstanding under the August 2024 Nirland Note, within two business days following the closing of such financing, in an amount of no less than 75% of the net proceeds received. Per the terms of the August 2024 Nirland Note, the Company was prohibited from entering into a ~~variable~~ variable rate transaction without prior written consent from Nirland. The August 2024 Nirland Note bore interest at a rate of 12% per annum, accruing daily on a 365-day basis, payable monthly in arrears as cash, or accrued at Nirland’s discretion. ~~The~~ The August 2024 Nirland Note was scheduled to mature 12 months from August 6, 2024.

On October 31, 2024, the Company and Nirland amended the August 2024 Nirland Note (the “First Amendment”), whereby the August 2024 Nirland Note was amended to (i) provide for the conversion of the August 2024 Nirland Note into shares of Common Stock, at Nirland’s discretion, in a multiple of any unpaid amounts, if not otherwise previously paid, pursuant to the conversion rate contained therein, (ii) remove Nirland’s Mandatory Prepayment Right, and (iii) remove Nirland’s right of first refusal to participate in any future equity or debt offerings of the Company. The number of shares of Common Stock issuable upon conversion of any Conversion Amount would be determined by dividing (x) such conversion amount by (y) the conversion price. Conversion amount means two and one quarter times the sum of (x) portion of the principal to be converted, redeemed or otherwise with respect to which this determination is being made and (y) all accrued and unpaid interest with respect to such portion of the principal amount, if any. Conversion price means, as of any conversion date or other date of determination, $10.00, subject to adjustment as provided within the amended agreement.

The Company evaluated the conversion feature of this note offering for embedded derivatives in accordance with ASC Topic 815, Derivatives and Hedging, and the substantial premium model in accordance with ASC Topic 470, Debt. Based on our assessment, ~~separate~~ separate accounting for the conversion feature of this note offering is not required and will be accounted for under the substantial ~~premium~~ premium model. Under the substantial premium model, the excess above the fair value of the August 2024 Nirland Note will be recorded in in additional paid-in-capital. The August 2024 Nirland Note was carried at amortized cost using the effective interest method. The Company accounted for the First Amendment as a debt extinguishment, as the First Amendment added a substantive conversion option.

On November 22, 2024, the Company and Nirland entered into a Second Amendment to the August 2024 Nirland Note (the “Second Amendment”). Pursuant to the Second Amendment, the August 2024 Nirland Note may not be converted (other than partial conversions that may be permitted ~~pursuant~~ pursuant to the rules and regulations of Nasdaq (or any successor entity)) prior to receipt of stockholder approval to provide for such ~~conversion~~ conversion of the August 2024 Nirland Note, and subsequent issuance of the Company’s Common Stock, pursuant to the stockholder approval rules under the rules and regulations of The Nasdaq Stock Market. If the Company had not held a special meeting of the stockholders to approve the full conversion of the August 2024 Nirland Note on or before January 9, 2025, then the Company was obligated to pay Nirland a penalty of $0.1 million per day until the special meeting was held. In addition, the existing conversion rate was amended to be two and one half times the sum of (x) the portion of the principal to be converted, redeemed or otherwise with respect to which this determination is being made and (y) all accrued and unpaid interest (including default interest) with respect to such portion of the principal amount, if any divided by $0.10, prior to the Reverse Stock Split, (or following any reverse splits that may occur in a ratio greater than 10 to 1, the lower of such reverse split price and the market price per share at the time of the Conversion Date, but in no event less than $1.00), subject to adjustment as provided therein and to take into account any future share splits or reverse splits to maintain the ~~economic~~ economic equivalence of the conversion rights as at the amendment effective date. The Company notes that the reverse split provision in the preceding sentence was tripped, ~~effective January 25, 2025,~~ following the ~~1-for-100~~January ~~reverse~~Reverse ~~stock~~Stock ~~split that occurred on that date~~Split.

As of the Second Amendment, the Company elected to account for the August 2024 Nirland Note at fair value under ASC 825. The Company determined that the amendment to the conversion features present in the Second Amendment fall under the guidance within ASC 825 that notes that if a significant modification of debt occurs an entity is able to make an accounting election on that date to account for that debt under the fair value option. At the end of each reporting period, the Company calculates the fair value of the August 2024 Nirland Note, and any changes in fair value are reported in the current period’s condensed consolidated statements of operations and comprehensive loss.

The Company remeasured the fair value of the August 2024 Nirland Note as of the Second Amendment date and calculated a fair value of $4.5 million using a binomial lattice model. On December 9, 2024, and prior to obtaining shareholder approval, Nirland exercised their conversion option and converted $0.1 million of principal for 23,000 shares of common stock pursuant to the rules and regulations of the Nasdaq. As of December 31, 2024, $2.6 million of principal and accrued interest remained outstanding and the August 2024 Nirland Note had a fair value of $2.8 million.15

14The Company remeasured the fair value of the August 2024 Nirland Note as of the Second Amendment date and calculated a fair value of $4.5 million using a binomial lattice model. On December 9, 2024, and prior to obtaining shareholder approval, Nirland exercised their conversion option and converted $0.1 million of principal for 1,533 shares of Common Stock pursuant to the rules and regulations of the Nasdaq. As of December 31, 2024, $2.6 million of principal and accrued interest remained outstanding and the August 2024 Nirland Note had a fair value of $2.8 million.

During January and February 2025, Nirland exercised their conversion option and converted $1.8 million of principal in exchange for ~~901~~60,~~200~~080 shares of ~~common~~Common ~~stock~~Stock. In total the Company issued ~~common~~Common ~~stock~~Stock with a fair value of $3.7 million based on the closing stock price on each conversion date and recorded a loss on the change in fair value of $1.9 million, calculated as the difference between the fair value of the shares issued and the portion of principal and interest settled. On February 12, 2025, the Company repaid the remaining unpaid principal and interest of $0.9 million in cash and recorded a gain on extinguishment of $0.1 million, calculated as the difference between the remaining fair value of August 2024 Nirland Note, less the amount of cash paid. As of ~~March~~June 3130, 2025, no obligations remained under the August 2024 Nirland Note.

For the three and six months ended ~~March~~June 3130, 2025, the Company recorded $24,000 of interest expense, presented within Interest expense, net, in the condensed consolidated statement of operations and comprehensive loss.

A.G.P. Convertible Note

OnA.G.P was a financial advisor ~~November~~to ~~25,~~both ~~2024,~~MURF ~~the~~and ~~Company~~Old ~~issued~~Conduit toin Aconnection with the Merger transaction.~~G.P.~~ Upon the “completion of the Merger, A.G.P.: ~~Convertible~~(i) ~~Note~~received a cash fee of $6.5 million, 867 shares of Common Stock, and warrants to purchase 36 shares of Common Stock at an exercise price of $16,500 per share pursuant to its engagement agreement with Old Conduit entered into on August 2, 2022, and (ii) agreed to defer payment, to be paid in the ~~principal amount~~future under certain circumstances by a date no later than March 21, 2025, of $5.7 million toof ~~evidence A.G.P.’s~~fees ~~currently~~plus ~~owed~~annual ~~deferred~~interest ~~commission~~of ~~payable~~5.5% (the ~~Refer~~“Deferred ~~to Note~~Commission 6Payable”) as a result of its engagement for ~~additional information~~MURF’s IPO. ~~Unless~~Accrued ~~earlier~~interest ~~converted~~was recorded as ~~specified~~a liability inon the ~~Convertible~~Company’s ~~Note,~~consolidated ~~the~~balance ~~principal~~sheet ~~amount,~~under ~~plus~~accrued ~~all~~expenses ~~accrued~~and ~~but~~other ~~unpaid~~current ~~interest,~~liabilities and totaled $0.4 million isas ~~due~~of onDecember ~~November~~31, 252024. During the six months ended June 30, 2025, (the ~~“Maturity~~Company ~~Date”)~~reached an agreement with A.G.P. ~~The~~to ~~convertible~~waive ~~promissory~~all ~~note~~previously accrued ~~accrues~~interest. As such, the Company removed accrued interest atof 5$0.5%4 ~~per~~million ~~annum~~and recorded other income of $0.4 million for the six months ended June 30, 2025.

~~At any~~For ~~time prior to~~ the ~~full~~three ~~payment~~and ofsix ~~the~~months ~~convertible promissory note, provided that the A.G.P. has given at least three business~~ended ~~days~~June ~~written notice to the Company~~30, ~~A.G.P.~~2025, ~~in its sole discretion, may elect to have all or any portion of~~ the ~~outstanding principal amount and all interest accrued converted into shares of the~~ Company’s ~~common~~recorded ~~stock, at a fixed price of~~ $100.~~00 (or following any reverse splits that may occur in a ratio greater than 10 to~~ 1, ~~the~~million ~~lower of such reverse split price~~ and ~~the market price per share at the time of the conversion date, but in no event less than~~ $10.~~00 (the~~2 ~~“Conversion~~million ~~Price~~of ~~Floor”),~~interest ~~subject~~expense torelated ~~adjustment as provided therein and~~ to ~~take~~the ~~into~~deferred ~~account~~commission ~~any~~payable ~~future share splits or reverse splits. The~~balance ~~Company~~in ~~notes that~~ the ~~reverse~~condensed ~~split~~consolidated ~~provision~~statement inof ~~the~~operations ~~preceding~~and ~~sentence~~comprehensive ~~was~~income ~~tripped~~loss, ~~effective January 25, 2025, following the 1-for-100 reverse stock split that occurred on that date~~respectively.

~~Per~~On ~~the~~November ~~terms of the A.G.P. Convertible Note~~25, ~~conversion could not occur prior to the Company having sufficiently authorized shares of common stock to permit the entire conversion of the convertible promissory note. In addition~~2024, ~~the conversion of the convertible promissory note~~ ~~could also not occur prior to receipt of stockholder approval to provide for such conversion of~~ the ~~convertible promissory note, and subsequent issuance of the~~ Company’s ~~common~~issued ~~stock, pursuant~~ to ~~the~~A.G.P. ~~stockholder approval rules under~~ the ~~rules and regulations of The Nasdaq Stock Market. Further,~~ “A.G.P. ~~will~~Convertible ~~not~~Note bein ~~entitled to receive~~ the ~~Company’s~~principal ~~common~~amount ~~stock~~of ~~upon~~$5.7 ~~conversion,~~million ~~if such~~to ~~conversion~~evidence ~~would result in~~ A.G.P.’s ~~owning greater than 9.99%~~currently ofowed ~~the~~Deferred ~~Company’s~~Commission ~~then~~Payable, ~~currently~~at ~~outstanding~~which ~~common~~time ~~stock.~~the ~~A.G.P.~~Deferred isCommission ~~also~~Payable ~~entitled~~balance towas ~~resale~~removed. ~~registration~~Unless ~~rights~~earlier converted as ~~identified~~specified in the ~~convertible~~Convertible ~~promissory~~Note, ~~note.~~the Asprincipal ofamount, ~~January~~plus ~~25,~~all ~~2025,~~accrued ~~the~~but ~~Company~~unpaid ~~had~~interest, ~~sufficient~~is ~~authorized~~due ~~shares~~on ofNovember ~~common~~25, ~~stock~~2025 to(the ~~permit~~“Maturity ~~the~~Date”). ~~entire~~The ~~conversion of the~~ convertible promissory note ~~and~~accrues ~~the~~interest ~~Company~~at ~~has~~5.5% ~~also~~per ~~received shareholder approval to allow for the entire conversion of the convertible promissory note~~annum.

~~The~~Per ~~Company~~the ~~may~~terms ~~prepay~~of the ~~convertible~~A.G.P. ~~promissory~~Convertible ~~note~~Note, inconversion ~~whole~~could ornot inoccur ~~part.~~prior Into the ~~event~~Company ofhaving ~~certain~~sufficiently ~~Events~~authorized shares of ~~Default~~Common ~~(as~~Stock ~~defined~~to inpermit the entire conversion of the convertible promissory note). In addition, ~~all~~the ~~outstanding~~conversion ~~principal~~of the A.G.P. Convertible Note could also not occur prior to receipt of stockholder approval to provide for such conversion, and subsequent ~~accrued~~issuance ~~interest~~of the Company’s Common Stock, pursuant to the stockholder approval rules under the ~~Convertible~~rules ~~Note~~and ~~will~~regulations ~~become~~of The Nasdaq Stock Market. Further, orA.G.P. ~~may~~will ~~become~~not atbe entitled to receive the Company’s Common Stock upon conversion, if such conversion would result in A.G.P. owning greater than 9.99% of the Company’s ~~election~~then currently outstanding Common Stock. A.G.P. is also entitled to resale registration rights as identified in the A.G.P. Convertible Note. As of January 25, ~~immediately~~2025, ~~due~~the ~~and~~Company ~~payable~~had sufficient authorized shares of Common Stock to permit the entire conversion of the A.G.P. Convertible Note and the Company had also received shareholder approval to allow for the entire conversion of the convertible promissory note.

The Company may prepay the A.G.P. Convertible Note in whole or in part. In the event of certain Events of Default (as defined in the A.G.P. Convertible Note), all outstanding principal and accrued interest under the A.G.P. Convertible Note will become, or may become at A.G.P.’s election, immediately due and payable to the A.G.P.

The Company elected to account for the A.G.P. Convertible Note at fair value under ASC 825. The Company determined that the substantive conversion option within the A.G.P. Convertible Note falls under the guidance within ASC 825 that notes that if a significant modification of debt occurs an entity is able to make an accounting election on that date to account for that debt under the fair value option. At the end of each reporting period, the Company calculates the fair value of the A.G.P. Convertible Note, and any changes in fair value are reported in the current period’s condensed consolidated statements of operations and comprehensive loss. The change in fair value attributable to instrument-specific credit risk, if any, will be recognize within other comprehensive income each reporting period. As an accounting policy, the Company elected to present interest expense separately from other changes in the A.G.P. Convertible Note’s fair value. Interest expense will be presented within Interest expense, net, while the other changes in the fair value with be presented within other income (expense), net in the condensed consolidated statements of operations and comprehensive loss.

15The Company determined the fair value of the A.G.P. Convertible Note to be $3.4 million as of November 25, 2024 through the use of a binomial lattice model. See Note 2 for additional information regarding the fair value measurement of the A.G.P Convertible Note. As of December 31, 2024, $6.1 million of principal and accrued interest remained outstanding and the A.G.P. Convertible Note had a fair value of $3.0 million.

~~The~~On ~~Company~~March ~~determined~~31, ~~the~~2025, ~~fair value of the~~ A.G.P. ~~Convertible~~exercised ~~Note~~their toconversion beoption and converted $30.4 million as of ~~November~~principal 25and interest in exchange for 28,667 shares ~~2024~~of ~~through~~Common ~~the~~Stock. ~~use~~As of aMarch ~~binomial~~31, ~~lattice~~2025, ~~model.~~the ~~See~~Company’s ~~Note~~Common 2Stock ~~for~~price ~~additional~~was ~~information~~trading ~~regarding~~below the ~~fair~~Conversion ~~value~~Price Floor. For ~~measurement~~the purpose of the March 31, 2025 conversion, the Company waived the Conversion Price Floor and allowed A.G.P. ~~Convertible~~to ~~Promissory~~convert ~~Note.~~at Asthe ofprior trading ~~December~~days ~~31,~~closing ~~2024~~stock price. Upon conversion, the Company recorded a $60.12 million loss on the change in fair value based on the difference between (i) the fair value of ~~principal~~the Common Stock issued and ~~accrued~~(ii) ~~interest~~the ~~remained~~percentage ~~outstanding~~of total principal and ~~the~~interest Aconverted (6.~~G.P.~~54%), multiplied ~~Convertible~~by ~~Note~~the ~~had~~December a31, ~~fair~~2024 ~~value~~valuation of $3.0 million.

On ~~March~~April 3111, 2025, April 16, 2025, June 2, 2025, June 17, 2025, and June 26, 2025, the holder of the A.G.P. ~~exercised~~Convertible ~~their~~Note ~~conversion~~converted ~~option~~$0.5 million, ~~and~~$0.8 ~~converted~~million, $0.4 1 million, $0.2 million, and $0.2 million of principal and interest ininto ~~exchange~~28,666, ~~for~~71,026, ~~430~~40,000, 90,000, and 100,000 shares of ~~common~~the ~~stock~~Company’s Common Stock, respectively. As of ~~March~~April 3116, 2025, the Company’s ~~common~~Common ~~stock~~Stock price was trading below the Conversion Price Floor. For the purpose of the ~~March~~April 3116, 2025 conversion, the Company waived the Conversion Price Floor and allowed A.G.P. to convert at ~~a price~~the ofApril ~~$0.89/share~~16, ~~(prior~~2025 ~~trading day~~ closing stock price). Upon conversion, the Company recorded a $0.2 million loss on the change in fair value based on the difference between (i) the fair value of the common stock issued and (ii) the percentage of total principal and interest converted (6.54%), multiplied by the December 31, 2024 valuation of $3.0 million.

~~Additionally,~~On onJune ~~March 31~~30, 2025, the Company remeasured the fair value of the A.G.P. Convertible Note through the use of a binomial lattice model and ~~calculated~~ calculated a fair value of approximately $21.7 9 million. For the three months ended ~~March~~June 3130, 2025, the Company recorded a $0.2 1 million loss in the change in fair value of the A.G.P. Convertible Note and interest expense of approximately $0.1 million. For the six months ended June 30, 2025, the Company recorded a $0.1 million gain in the change in fair value of the A.G.P. Convertible Note and interest expense of approximately $0.1 million. As of ~~March~~June 3130, 2025, there was approximately $53.56 million in outstanding principal and interest remaining.

5. Loans Payable

Loans

On May 1, 2022, the Company entered into Loan Agreements (the “Loans”) with two lenders, totaling $0.2 million. The Loans mature two years from the date of the agreement and bear no interest. Each loan was made available to the Company by the lenders in three tranches of (i) $33,000 (£30,000); (ii) $33,000 (£30,000) ; and (iii) $28,000 (£25,000)~~, totaling $0~~.~~2 million.~~ The Loans provided for events of default, including, among others, failure to make payment, bankruptcy and non-compliance with the terms of the Loans. As of December 31, 2024, the Company utilized all three tranches of the first loan and two out of three tranches of the second loan, with loans payable totaling $0.2 million.

On October 9, 2024, the Company and holders of the Loans amended the loan agreements (the “Loans Amendment”) to extend the maturity date for the Loans to December 19, 2024. The Loans Amendment also modified the payment terms for the Loans from a cash payment of £85,000 per loan to (1) a cash payment of £60,000, (2) £25,000 worth of shares of Common Stock converted into USD at the prevailing exchange rate, to be issued at the closing market price on the date prior to issuance, and in consideration for the extension, and (3) ~~2,500~~ 167 additional shares of Common stock. On October 11, 2024, the Company issued each of the Loan holders ~~5,690~~ 379 shares (~~11,380~~ 758 shares in total).

The Company repaid the lenders the outstanding principal balance of $0.1 million in February 2025, in which no obligations remain under the terms of the Loans. No interest expense was recorded for each of the three months ended March 31, 2025 and March 31, 2024.17

October 2024 Nirland Note

On October 28, 2024, the Company issued a promissory note (the “October 2024 Nirland Note”) to Nirland, a related party, in the original principal amount of $0.6 million in exchange for funds in such amount. See Note 1615 for further reference to the relationship between the Company and Nirland. The October 2024 Nirland Note bore interest at a rate of 12% per annum, was due and payable semi-annually in arrears, and was scheduled to mature on October 31, 2025. If an event of default under and as defined in the October 2024 Nirland Note occurs, the interest rate would ~~have been~~ be increased to 18% per annum or to the maximum rate permitted by law. In connection with the October 2024 Nirland Note, the Company has agreed to pay Nirland a 1% arrangement fee, which was included with the principal and interest owed under the October 2024 Nirland Note. The 1% arrangement fee is accounted for as a debt discount and was amortized to interest expense, net in the consolidated statement of operations and comprehensive income (loss) using the effective interest method over the life of the October 2024 Nirland Note.

On December 11, 2024, the Company reduced the exercise price of the PIPE Warrants held by Nirland to $8.83, at which time all PIPE Warrants were exercised. The Company received approximately $0.2 million of proceeds from the exercise of the Warrants, all of which were used to pay down the October 2024 Nirland Note.

The Company repaid principal and interest of $0.1 million, $0.2 million, and $0.1 million on January 14, 2025, January, 31, 2025, and February 7, 2025, respectively. As of ~~March~~June 3130, 2025, no obligations remain under the October 2024 Nirland Note.

During the three and six months ended ~~March~~June 3130, 2025, the Company recorded zero and approximately $8,000 of interest expense, respectively.

~~6. Deferred Commission Payable~~18

~~A.G.P was a financial advisor to both MURF and Old Conduit in connection with the Merger transaction. Upon the completion of the Merger, A.G.P.: (i) received a cash fee of $~~6.~~5 million, 13,000 shares of Common Stock, and warrants to purchase 540 shares of Common Stock at an exercise~~ ~~price~~Research ~~of $1,100 per share pursuant to its engagement agreement with Old Conduit entered into on August 2, 2022,~~ and ~~(ii)~~Development agreed to defer payment, to be paid in the future under certain circumstances by a date no later than March 21, 2025, of $5.7 million of fees plus annual interest of 5.5% as a result of its engagement for MURF’s IPO. Accrued interest was recorded as a liability on the Company’s consolidated balance sheet under accrued expenses and other current liabilities and totaled $0.4 million as of December 31, 2024. During the three months ended March 31, 2025, the Company reached an agreement with A.G.P. to waive all previously accrued interest. As such, the Company removed accrued interest of $0.4 million and recorded other income of $0.4 million for the three months ended March 31, 2025.Expense

On November 25, 2024, the Company issued the A.G.P. Convertible Note in the principal amount of $5.7 million to evidence the currently owed deferred commission payable, at which time the deferred commission payable balance was removed. Refer to Note 4 for additional information.

For the three months ended March 31, 2024, the Company recorded $0.1 million of interest expense related to the deferred commission payable balance in the condensed consolidated statement of operations and comprehensive income loss.

7. Research and Development Expense

August 2024 License Agreement

On August 7, 2024, the Company and AstraZeneca AB (PUBL) (“AstraZeneca”) entered into a License Agreement, dated August 7, 2024 (the “August 2024 License Agreement”). Pursuant to the August 2024 License Agreement, AstraZeneca agreed to grant a license to the Company under certain intellectual property rights controlled by AstraZeneca related to HK-4 Glucokinase activators AZD1656 and AZD5658 in all indications and myeloperoxidase inhibitor AZD5904 for the treatment, prevention, and prophylaxis of idiopathic male infertility. The Company will be responsible for the development and commercialization of the Licensed Products under the August 2024 License Agreement.

As consideration for the grant of the license, the Company (i) granted AstraZeneca Common Stock pursuant to a stock issuance agreement (the “Issuance Agreement”), (ii) paid AstraZeneca an up-front payment of $1.5 million, and (iii) is obligated to pay AstraZeneca a percentage (on a tiered basis) of any amounts it may receive in connection with a grant of a sublicense (subject to various customary exceptions). The Issuance Agreement called for the Company to issue AstraZeneca 956,~~044~~ 336 shares of the Company’s Common Stock. The Issuance Agreement provides AstraZeneca with resale registration rights for such shares.

17AstraZeneca has been granted a right of first negotiation to develop, manufacture, and commercialize a Licensed Product (as defined in the August 2024 License Agreement) if the Company receives an offer for, or solicits, a transaction where a third party would obtain the right to develop, manufacture, or commercialize a Licensed Product. If AstraZeneca exercises such right, the parties will negotiate in good faith for an agreed period of time on an exclusive basis.

AstraZeneca has been granted a right of first negotiation to develop, manufacture, and commercialize a Licensed Product if the Company receives an offer for, or solicits, a transaction where a third party would obtain the right to develop, manufacture, or commercialize a Licensed Product. If AstraZeneca exercises such right, the parties will negotiate in good faith for an agreed period of time on an exclusive basis.

Either party may terminate the August 2024 License Agreement for material breach (subject to a cure period) or insolvency of the other party. The Company may terminate the August 2024 License Agreement for convenience (in its entirety or on a Licensed Product-by-Licensed Product basis). In addition, AstraZeneca may terminate the August 2024 License Agreement in certain circumstances, including (but not limited to) the Company ceasing development of all Licensed Products (subject to certain exceptions for normal pauses or gaps between clinical studies).

As a result of the above, the Company is no longer funding the development of AZD1656 or AZD5904 under the terms of the Exclusive Funding Agreement, dated March 26, 2021 with St George Street Capital (the “Funding Agreement”). In this regard, the Company previously entered into a deed of amendment amending such Funding Agreement. The parties agreed that the project funding provisions of such Funding Agreement whereby the Company had the right to fund a project or refer other parties to St George Street Capital, were amended to provide that St George Street Capital must still include the Company in any project funding opportunities and requests but may now seek other third-parties to fund projects in addition to the Company. In November and December 2024, the Company received a letter from St George Street Capital and formal complaints filed with the Intellectual Property Office claiming the Company was not the sole owner of the AZD 1656 co-crystal patent. See Note 1514 for additional details on the claim.

SARBORG Service Agreement – Related Party

On December 12, 2024, the Company entered into a Services Agreement (the “Sarborg Service Agreement”) with SARBORG Limited (“Sarborg”), a Cayman Islands company and related party of the Company. See Note 1211 for further reference to the relationship between the Company and Sarborg. Under the terms of the Sarborg Service Agreement, Sarborg will provide algorithmic and cybernetic technology services to ~~Conduit~~CDT, including the development of decision-support tools and advanced cybernetic systems tailored to enhance ~~Conduit~~CDT’s decision-making processes and maximize the value of its pharmaceutical asset portfolio.

Sarborg will perform the services to ~~Conduit~~CDT comprised of three phases: the Initial Phase (0-24 weeks) focuses on establishing a foundation for collaboration and aligning Sarborg’s services with ~~Conduit~~CDT’s strategic goals; the Development Phase (24-36 weeks) involves building technological infrastructure, including dashboards and predictive models; and the Ongoing Services Phase (36-52 weeks) ensures the sustained functionality and relevance of Sarborg’s deliverables while supporting ~~Conduit~~CDT’s growth through iterative improvements and updates. Sarborg will create specific deliverables, including reports, computer programs, software applications, APIs, mobile applications, source code, written technical specifications and designs, operating and maintenance manuals, and other recorded data and information arising from or relating to the services. Sarborg will provide all necessary resources to perform the services and deliver the deliverables in accordance with the Sarborg Service Agreement.

The Sarborg Service Agreement has an initial term of 12 months, which commenced in December 2024, and may be renewed or extended upon mutual written agreement of the parties. Either party may terminate the Sarborg Service Agreement for any reason upon 90 days’ written notice or immediately upon written notice if the other party breaches any material term of the Sarborg Service Agreement and fails to cure such breach within thirty days or becomes insolvent, files for bankruptcy, or is placed under the control of a receiver, trustee, or similar authority.

The Sarborg Service Agreement includes provisions for the ownership and use of intellectual property. Sarborg will own its pre-existing intellectual property rights, including proprietary tools and methodologies used in the performance of the services. ~~Conduit~~CDT will own all deliverables resulting from the services performed by Sarborg under the Sarborg Service Agreement.

18The Sarborg Service Agreement provides Sarborg with registration rights for any Common Stock of CDT that Sarborg receives as consideration under the Sarborg Service Agreement. In such event, CDT will use commercially reasonable efforts to (i) file a registration statement covering the resale of the Common Stock within 60 days after the issuance; and (ii) ensure that such registration statement becomes effective within 90 days after filing. This Agreement also includes confidentiality obligations, representations and warranties, indemnification, limitation of liability, and insurance requirements.

~~The~~In ~~Sarborg~~consideration ~~Service~~of ~~Agreement~~the ~~provides~~services, CDT agreed to pay Sarborg ~~with~~an ~~registration~~initial ~~rights~~cash ~~for~~payment ~~any~~of $0.2 million and $0.2 million payable through the issuance of 1,515 shares of Common Stock, ofdetermined ~~Conduit~~by ~~that~~the ~~Sarborg~~closing ~~receives~~price ason ~~consideration under~~the day preceding the execution of the Sarborg Service Agreement. InThe initial ~~such~~cash ~~event,~~payment ~~Conduit~~of ~~will~~$0.2 million ~~use~~was ~~commercially~~made ~~reasonable~~on ~~efforts~~December to20, ~~(i)~~2024, ~~file~~and athe ~~registration statement~~1,515 ~~covering~~shares ~~the resale~~ of ~~the~~ Common Stock ~~within~~were 60issued ~~days~~on ~~after~~January ~~the~~17, ~~issuance;~~2025. ~~and~~Further ~~(ii)~~milestone ~~ensure~~payments ~~that~~payable ~~such~~in ~~registration~~conjunction ~~statement~~with ~~becomes~~the ~~effective~~achievement of ~~within~~certain 90milestones ~~days~~over ~~after~~the ~~filing.~~term ~~This~~of the Sarborg Service Agreement, ~~also~~totaling ~~includes~~up ~~confidentiality~~to ~~obligations~~$1.8 million, ~~representations~~are ~~and~~payable ~~warranties,~~in ~~indemnification~~cash or stock, ~~limitation~~ at the discretion of ~~liability~~CDT. Sarborg will be reimbursed for pre-approved, necessary, and reasonable ~~insurance~~out-of-pocket ~~requirements~~expenses directly incurred in connection with the performance of the services.

~~In consideration~~The ~~of the services, Conduit agreed to pay Sarborg an~~ initial cash payment of $0.2 ~~million~~ million and ~~$0.2 million payable through the~~ issuance of 221,~~727 shares~~515 shares of ~~common~~ ~~stock,~~Common ~~determined~~Stock bywere ~~the~~recorded ~~closing~~to ~~price~~prepaid onexpense ~~the~~and ~~day~~will ~~preceding~~be amortized over the ~~execution~~initial term of the Sarborg Service Agreement. to ~~The~~research ~~initial~~and ~~cash~~development ~~payment~~expense. ofFor ~~$0.2~~the ~~million~~three ~~was~~and ~~made~~six onmonths ~~December~~ended 20June 30, ~~2024~~2025, ~~and~~ the ~~22,727~~Company ~~shares~~recorded ofamortization ~~common~~expense ~~stock~~of $0.1 ~~were~~million and ~~issued~~$0.2 ~~on January~~million, 17respectively, ~~2025.~~with ~~Further~~research ~~milestone~~and ~~payments~~development ~~payable~~expense in ~~conjunction~~the ~~with~~condensed ~~the~~consolidated ~~achievement~~statement of ~~certain~~operations ~~milestones~~and ~~over~~comprehensive ~~the term of the Sarborg~~income ~~Service Agreement~~loss, ~~totaling up to $1~~respectively.~~8 million,~~ ~~are~~As ~~payable in cash or shares, at the discretion~~ of ~~Conduit.~~June ~~Sarborg will be reimbursed for pre-approved~~30, ~~necessary~~2025, ~~and~~$0.2 ~~reasonable~~million ~~out-~~of~~-pocket~~ ~~expenses~~the ~~directly~~prepaid ~~incurred~~balance inremains ~~connection~~within ~~with~~ the ~~performance~~condensed ofconsolidated ~~the~~balance ~~services~~sheets.

~~Management determined~~Under ~~that~~ the ~~cost~~Sarborg ~~incurred~~Service ~~under~~Agreement, the Company ~~Sarborg~~will ~~Service~~be ~~Agreement~~provided ~~should~~with a dashboard that will be ~~recorded~~utilized tofor ~~research~~both the Company’s existing and ~~development~~future ~~expense~~asset inportfolio. Specifically, the ~~condensed consolidated~~dashboard ~~statement~~includes ofa ~~operations~~clinical trial monitoring functionality and ~~comprehensive~~a dynamic ~~income~~pharmaceutical ~~loss,~~patent aslandscape module to assess both the ~~Sarborg~~Company’s ~~Service~~current ~~Agreement~~assets isundergoing ~~designed~~clinical totrials ~~provide~~and delisted patents in the ~~Company with~~marketplace ~~software/dashboard~~that may be overlooked by other market participants. These features will be used by management to ~~aid~~monitor inprogress, assess ~~research~~trial status, identify new opportunities, and support decision-making across all current and future development ~~activities~~programs. The ~~initial~~Company assessed ~~cash~~the ~~payment~~guidance ofin ASC 730 and determined that $0.24 million ~~and~~of ~~issuance~~total cost of ~~22,727 shares~~the ofacquired ~~Common~~asset ~~Stock~~should ~~were~~be ~~recorded~~capitalized toas ~~prepaid~~the ~~expense~~dashboard is ~~and~~considered ~~will~~a bepurchased ~~amortized~~diagnostic ~~over~~asset ~~the~~with ~~initial~~alternative ~~term~~future ofuse. Management determined that the ~~Sarborg~~dashboard ~~Service~~has ~~Agreement~~a useful life of totwo ~~research~~years. ~~and~~The ~~development~~dashboard ~~expense~~was placed in service on March 18, 2025. ~~For~~During the three and six months ended ~~March~~June 3130, 2025, the Company recorded ~~amortization expense of~~ $~~0.1~~50 ~~million with~~thousand ~~research~~ and ~~development~~$57 ~~expense~~thousand in ~~the~~amortization ~~condensed~~expense, ~~consolidated statement of operations and comprehensive income loss~~respectively.

~~During~~All ~~the~~other ~~three~~costs ~~months ended March 31, 2025, Sarborg was paid $1.1 million for completed milestones~~ under the Sarborg Service Agreement. ~~The Company~~shall ~~recorded~~be ~~the~~expensed ~~$1.1~~as ~~million~~incurred inand ~~expense~~recorded within research and development expense in the condensed consolidated statement of operations and comprehensive income loss, ~~for~~as the ~~three~~services ~~months~~are ~~ended~~designed ~~March~~to ~~31,~~aid ~~2025~~in the Company’s research and development activities.

~~Master~~During the three and six months ended June 30, 2025, Sarborg was paid $0.5 million and $1.2 million, respectively, for completed milestones under the Sarborg Service Agreement –and ~~Conduit~~had an outstanding payable balance of $0.2 million as of June 30, 2025. The Company recorded $0.7 million and ~~Charles~~$1.5 ~~River~~million ~~Laboratories~~in expense within research and development expense in the condensed consolidated statement of operations and comprehensive income loss for the three and six months ended June 30, 2025, respectively. The remaining $0.4 million was related to the delivery of the dashboard, which was recorded as a diagnostic asset on the condensed consolidated balance sheet as of March 31, 2025.

OnMaster ~~February~~Service ~~7, 2025, the Company and Charles River Laboratories (“Charles River”) entered into a Master Services~~ Agreement ~~(the~~ ~~“Charles~~– ~~River~~CDT ~~MSA”).~~Equity ~~Under the Charles River MSA, Charles River agreed to provide preclinical testing and research services to Conduit, including the evaluation of compounds in animal models and other related services~~Inc. ~~The services are defined in individual Statements of Work (“SOWs”) or Protocols, which outline the specific scope, design,~~ and ~~timelines for each study. To date, one SOW, dated February 11, 2025, has been entered into with a total commitment of $0.2 million.~~ Charles River will conduct the studies in compliance with applicable laws and industry standards, and Conduit will provide necessary test articles and materials. The Charles River MSA includes provisions for confidentiality, intellectual property ownership, indemnification, and dispute resolution. The Charles River MSA has a term of five years and can be terminated by either party under specified conditions. For the three months ended March 31, 2025, the Company recognized $0.1 million in research and development expense in the condensed consolidated statement of operations and comprehensive loss related to the Charles River MSA.Laboratories

On February 7, 2025, the Company and Charles River Laboratories (“Charles River”) entered into a Master Services Agreement (the “Charles River MSA”). Under the Charles River MSA, Charles River agreed to provide preclinical testing and research services to CDT, including the evaluation of compounds in animal models and other related services. The services are defined in individual Statements of Work (“SOWs”) or Protocols, which outline the specific scope, design, and timelines for each study. To date, one SOW, dated February 11, 2025, has been entered into with a total commitment of $0.2 million. Charles River will conduct the studies in compliance with applicable laws and industry standards, and CDT will provide necessary test articles and materials. The Charles River MSA includes provisions for confidentiality, intellectual property ownership, indemnification, and dispute resolution. The Charles River MSA has a term of five years and can be terminated by either party under specified conditions. For the three and six months ended June 30, 2025, the Company recognized $0.1 million in research and development expense in the condensed consolidated statement of operations and comprehensive loss related to the Charles River MSA.

SARBORG Additional Agreement

Effective March 31, 2025, the Company entered into an additional license and use agreement (the “Sarborg Additional Agreement”) with Sarborg, a related party, covering certain additional deliverables and incorporating a new scope of work focused on analysis of the Company’s acquired AstraZeneca assets. The term of the Sarborg Additional Agreement is for six months and provides for the payment, in aggregate, of $2.0 million, which includes an up-front license fee for the term of such agreement, in cash or stock at the Company’s election at the closing price on the day preceding the effective date of such agreement. On March 31, 2025, the Company prepaid $1.65 million of the Sarborg Additional Agreement through the issuance of 1123,~~853,933~~595 fully vested unregistered shares of Common Stock. The Company recorded the shares issued under the Sarborg Additional Agreement at their fair value, as determined by the closing price of the Company’s Common Stock on March 30, 2025, $013.8935, and adjusted for an 7% discount for lack of marketability, as determined by a third-party valuation expert. Effective May 2, 2025, the term was extended to be 12 months from the effective date of the Sarborg Additional Agreement at no additional cost to the Company. The Company recorded the fair value of $1.5 million as a prepaid within the condensed consolidated balance sheets. During the three and six months ended June 30, as2025, nothe Company ~~services~~recorded ~~had~~research ~~been~~and ~~provided~~development asexpense of ~~March~~$0.5 million ~~31,~~within the condensed consolidated statements of operations and comprehensive loss related to the amortization of the prepaid. As of June 30, 2025, $1.0 million of the prepaid balance remains within the condensed consolidated balance sheets.

19During the three and six months ended June 30, 2025, Sarborg was paid $0.3 million for deliverables under the Sarborg Additional Agreement and had an outstanding payable balance of $0.1 million as of June 30, 2025. The Company recorded $0.4 million in expense within research and development expense in the condensed consolidated statement of operations and comprehensive income loss for the three and six months ended June 30, 2025.

Consulting Agreement

Effective March 25, 2025, the Company entered into a Consulting Agreement (the “Consulting Agreement”) with Thesprogen PC (“Thesprogen”), an expert in advising clients on strategies for pharmaceutical and biotech development. Total fees under the Consulting Agreement total to $0.3 million and was settled through the issuance of ~~337~~22,~~079~~472 fully vested unregistered shares of Common Stock on March 31, 2025. The Company recorded the shares issued under the Consulting Agreement at their fair value, as determined by the closing price of the Company’s Common Stock on March 30, 2025, $013.8935, and adjusted for a 7% discount for lack of marketability, as determined by a third-party valuation expert. The Company recorded the fair value of $0.3 million as a prepaid within the condensed consolidated balance sheets,. asDuring ~~no services~~the ~~had~~three ~~been~~and ~~provided~~six asmonths ofended ~~March~~June 3130, 2025, the Company recorded research and development expense of $0.1 million within the condensed consolidated statements of operations and comprehensive loss related to the amortization of the prepaid.

~~8. Share~~Manoira ~~Based~~Joint ~~Compensation~~Development Agreement

On ~~September~~June 223, ~~2023~~2025, inthe ~~connection~~Company ~~with~~entered ~~the~~into ~~Merger,~~a ~~the~~joint ~~Company~~development ~~adopted~~agreement (the ~~Conduit~~“Joint ~~Pharmaceuticals~~Development ~~Inc.~~Agreement”) ~~2023~~with ~~Stock~~Manoira Corporation ~~Incentive Plan~~ (~~the~~ “~~2023 Plan~~Manoira”). ~~The~~for ~~2023~~a ~~Plan~~term ~~became effective upon the closing~~ of ~~the~~one ~~Merger.~~year, ~~The~~which ~~2023~~will ~~Plan~~be ~~initially~~automatically ~~provided~~renewed for ~~the~~successive ~~issuance of~~one-year upterms ~~to 114,976 shares of Common Stock. Pursuant to the 2023 Plan’s “evergreen” provision, on February 6,~~unless ~~2025~~advance ~~and~~termination ~~January~~notice ~~10,~~is ~~2024,~~provided ~~the~~in ~~Company~~accordance ~~increased~~with the ~~number~~terms of ~~shares of Common Stock available for issuance under~~ the ~~2023~~Joint ~~Plan~~Development ~~by 69,240 and 36,914 shares, respectively~~Agreement. ~~The~~Manoira ~~number~~is ofan ~~authorized shares will automatically increase on January 1, 2026 and continuing annually~~entity oncontrolled ~~each~~by ~~anniversary~~Dr. ~~thereof~~Andrew ~~through (and including) January 1~~Regan, ~~2033, equal to the lesser~~ of ~~(i) 5%~~which ofhe ~~the~~is ~~shares~~sole ofdirector, ~~common stock outstanding on the last day of the immediately preceding fiscal year~~ and ~~(ii)~~is ~~such~~therefore ~~smaller~~considered ~~number~~a ofrelated ~~shares~~party of ~~common stock as determined by~~ the ~~Board or the applicable committee of the Board~~Company. ~~The~~Refer ~~2023 Plan allows for awards~~ to ~~be issued to employees and non-employee directors~~ inNote ~~the~~11 form of options, stock appreciation rights, restricted stock, restricted stock units (“RSUs”), performance stock units, dividend equivalents, other stock-based, or other cash-based awards. As of March 31, 2025, there were 154,544 shares of Common Stock available for ~~issuance~~additional ~~under the 2023 Plan~~details.

OnPursuant ~~March 30, 2025, certain non-employee directors elected~~ to ~~receive~~the ~~their~~Joint ~~unpaid~~Development ~~cash retainers due as of March 31~~Agreement, ~~2025,~~CDT ~~and~~granted ~~cash retainers~~Manoira ~~owed~~a ~~for the period from April 1~~non-exclusive, ~~2025 to June 30~~non-transferable, ~~2025~~non-sublicensable, ~~under~~fully ~~the Director Compensation Program~~paid-up, ~~in the form of fully~~royalty-free ~~vested~~license ~~shares~~to ofthe ~~Common~~intellectual ~~Stock.~~property Inrights ~~total,~~related ~~$0.1 million of~~to ~~unpaid~~the ~~retainers~~pharmaceutical ~~was~~compounds ~~settled~~known ~~through~~individually ~~the~~and ~~issuance 155,257~~together ~~unregistered shares of~~as ~~Common~~AZD1656 ~~Stock~~and AZD5658 (the “~~Retainer~~CDT ~~Shares~~Assets”). ~~The~~Manoira ~~Company~~will ~~recorded~~evaluate the ~~Retainer~~CDT ~~Shares at their fair value, as determined by intraday share prices of the Company~~Assets’s ~~Common~~applicability ~~Stock~~in onanimal ~~March 31~~health, ~~2025.~~explore ~~The fair value of the shares issued for cash~~veterinary ~~retainers~~market ~~due as of March 31~~opportunities, ~~2025,~~and ~~$78,000,~~provide ~~was~~data ~~recorded~~from ~~within general & administration expense in~~ the ~~condensed~~evaluations ~~consolidated statement~~to ofinform ~~operations~~CDT’s ~~and~~human ~~comprehensive~~clinical ~~loss~~programs. The ~~fair~~license ~~value~~does ofnot ~~the~~grant Manoira ~~shares issued for cash retainers owed for~~ the ~~period~~right ~~from April~~to 1distribute, ~~2025~~market, topromote ~~June~~or ~~30,~~sell ~~2025,~~the ~~$58,000,~~products ~~was~~or ~~recorded~~services asthat aare ~~prepaid~~related ~~expense~~to inor incorporate the ~~condensed~~CDT ~~consolidated balance sheets~~Assets.

Effective June 3, 2025, in exchange for the approximate $0.5 million of consideration to be paid by CDT under the Joint Development Agreement, CDT issued to Manoira 154,799 shares of its Common Stock, (the “Consideration Shares”) valued at the closing price of the Common Stock immediately preceding execution of the Joint Development Agreement. The Company recorded the shares issued under the Joint Development Agreement at their fair value, as determined by the closing price of the Company’s Common Stock on June 2, 2025, $3.94, and adjusted for a 20% discount for lack of marketability, as determined by a third-party valuation expert. The Company recorded the fair value of $0.4 million as a prepaid within the condensed consolidated balance sheets. During the three and six months ended June 30, 2025, the Company did not record amortization expense, as no research and development activities had taken place.

7. Share Based Compensation

On September 22, 2023, in connection with the Merger, the Company adopted the CDT Equity Inc. 2023 Stock Incentive Plan (the “2023 Plan”). The 2023 Plan became effective upon the closing of the Merger. The 2023 Plan initially provided for the issuance of up to 7,665 shares of Common Stock. Pursuant to the 2023 Plan’s “evergreen” provision, on February 6, 2025 and January 10, 2024, the Company increased the number of shares of Common Stock available for issuance under the 2023 Plan by 4,616 and 2,461 shares, respectively. The number of authorized shares will automatically increase on January 1, 2026 and continuing annually on each anniversary thereof through (and including) January 1, 2033, equal to the lesser of (i) 5% of the shares of Common Stock outstanding on the last day of the immediately preceding fiscal year and (ii) such smaller number of shares of Common Stock as determined by the Board or the applicable committee of the Board. The 2023 Plan allows for awards to be issued to employees and non-employee directors in the form of options, stock appreciation rights, restricted stock, restricted stock units (“RSUs”), performance stock units, dividend equivalents, other stock-based, or other cash-based awards. As of June 30, 2025, there were 10,712 shares of Common Stock available for issuance under the 2023 Plan.

Board of Directors Shares

On March 30, 2025, certain non-employee directors elected to receive their unpaid cash retainers due through the period ended June 30, 2025, under the Director Compensation Program, in the form of fully vested shares of Common Stock. In total, $0.1 million of unpaid retainers was settled through the issuance 10,350 unregistered shares of Common Stock (the “Retainer Shares”). The Company recorded the Retainer Shares at their fair value, as determined by intraday share prices of the Company’s Common Stock on March 31, 2025. In relation to the Retainer Shares, the Company recorded $58,000 and $0.1 million of expense within general & administration expense in the condensed consolidated statement of operations and comprehensive loss during the three and six months ended June 30, 2025, respectively.

On April 15, 2025, 7,679 shares of the Company’s Common Stock were issued to a non-employee director. The shares were approved by the Board as a one-time award for services provided to the Company. The Company recorded the shares at their fair value, as determined by the Company’s closing share price on the prior trading day, April 14, 2025. The Company recorded $0.1 million within general & administration expense in the condensed consolidated statement of operations and comprehensive loss during the three and six months ended June 30, 2025 in relation to the shares.

Cryptocurrency Consulting

Effective June 27, 2025, the Company entered into an agreement (the “Crypto Consulting Agreement”) for a third-party consultant to evaluate and advise on the potential adoption of a part cryptocurrency treasury reserve strategy. The Crypto Consulting Agreement contains a term of 12 months and required compensation of $0.2 million in the form of shares of the Company’s Common Stock. On June 27, 2025, the Company issued 95,618 shares of Common Stock valued at the closing price for the previous day, $2.51. The $0.2 million of compensation was recorded as a prepaid expense in the condensed consolidated balance sheets. For the three and six months ended June 30, 2025, the Company recorded $3,000 of general and administrative expense within the condensed consolidated statements of operations and comprehensive loss related to the amortization of the prepaid.

Restricted Stock

No RSU’s or shares of restricted ~~common~~Common ~~stock~~Stock were granted during the three or six months ended ~~March~~June 3130, 2025 ~~and March 31, 2024~~. There were ~~745 shares~~ 50 shares of restricted ~~common~~Common ~~stock~~Stock vested as of ~~March~~June 3130, 2025 and ~~no RSUs~~ ~~vested~~June ~~as of March 31~~30, 2024.

Stock Options

The Company estimates the fair value of each option award on the date of grant using the Black-Scholes option-pricing model. The Company then recognizes the grant date fair value of each option as compensation expense ratably using the straight-line attribution method over the service period (generally the vesting period). The Black-Scholes model incorporates the following assumptions:

	●	Expected volatility – the Company estimates the volatility of the share price of their peer companies at the date of grant using a “look-back” period which coincides with the expected term, defined below. The Company believes using a “look-back” period which coincides with the expected term is the most appropriate measure for determining expected volatility.
	●	Expected term – the Company estimates the expected term using the “simplified” method outlined in SEC Staff Accounting Bulletin No. 107, “Share-Based Payment.”
	●	Risk-free interest rate – the Company estimates the risk- free interest rate using the U.S. Treasury Yield curve for periods equal to the expected term of the options in effect at the time of grant.
	●	Dividends – the Company uses an expected dividend yield of zero because the Company has not declared nor paid a cash dividend, nor are there any plans to declare a dividend.

The Company did not grant stock options during the three and six months ended ~~March~~June 3130, 2025 or ~~March~~June 3130, 2024.

The Company accounts for forfeitures as they occur, which may result in the reversal of compensation costs in subsequent periods as the forfeitures arise.

The following table summarizes stock option activity for the 2023 Plan:

Schedule of Stock Option Activity

	Number of Options			Weighted Average Exercise Price		Weighted Average Remaining Contractual Term (years)		Aggregate Intrinsic Value (in thousands)
Outstanding at December 31, 2024		654,~~509~~367		$	~~81.52~~1,223		9.72	$	-
Granted		-		$	-		-	$	-
Cancelled/forfeited		(~~419~~337	)	$	~~551~~1,484		-	$	-
Exercised		-		$	-		-	$	-
Outstanding at March 31, 2025		65,090		$	78.49		9.24	$	-
Outstanding at June 30, 2025		4,030		$	1,201		8.96	$	-
Exercisable		221,~~735~~516		$	~~75.57~~1,134		9.4823	$	-
Unvested		422,~~355~~514		$	~~84.68~~1,270		98.1085	$	-

The aggregate intrinsic value of options is calculated as the difference between the exercise price of the underlying options and the fair value of the Company’s ~~common~~Common ~~stock~~Stock for those options that had exercise prices lower than the fair value of the Company’s ~~common~~Common ~~stock~~Stock. As of ~~March~~June 3130, 2025, the total compensation cost related to non-vested option awards not yet recognized was $21.06 million with a weighted average remaining vesting period of 1.6441 years.

For the three months ended ~~March 31~~June 30, 2025 and ~~March~~June 3130, 2024, there was a total of $0.2 million and $0.45 million, respectively in stock-based compensation expense recognized within General and Administrative expenses on the condensed consolidated statements of operations and comprehensive loss, respectively.

9For the six months ended June 30, 2025 and June 30, 2024, there was a total of $0.4 million and $0.9 million, respectively in stock-based ~~Income~~compensation ~~Taxes~~expense recognized within General and Administrative expenses on the condensed consolidated statements of operations and comprehensive loss, respectively.

~~For the three months ended March 31, 2025, and 2024, the Company’s effective tax rate was 0~~8.~~0% and 0.0%, respectively, due to the current~~ ~~year~~Income ~~tax loss and valuation allowance established against the Company’s net deferred tax assets, and due to operating in a no tax jurisdiction, respectively.~~Taxes

21For the six months ended June 30, 2025, and 2024, the Company’s effective tax rate was 0.0% due to the current year tax loss and valuation allowance established against the Company’s net deferred tax assets, and due to operating in a zero tax jurisdiction, respectively.

109. Common Stock and Preferred Stock

At-the-Market Offering

On October 23, 2024, the Company entered into the Sales Agreement with A.G.P. (the “Sales Agreement”) relating to shares of the Company’s Common Stock. In accordance with the terms of the Sales Agreement, the Company may offer and sell shares of our Common Stock having an aggregate offering price of up to $23.9 million from time to time through A.G.P., acting as our sales agent or principal.

The compensation to A.G.P. for sales of ~~common~~Common ~~stock~~Stock sold pursuant to the Sales Agreement will be equal to 3.0% of the gross proceeds of any shares of ~~common~~Common ~~stock~~Stock sold under the sales agreement.

During the three and six months ended ~~March~~June 3130, 2025, the Company sold 41,~~345~~183,~~913~~ 221 and 1,472,945 shares of the Company’s Common Stock through the Sales Agreement, respectively. The Company received proceeds of $811.1 9 million, net of commissions payable to A.G.P. of $0.2 4 million. As of the date of this Quarterly Report on Form 10-Q, the Company has approximately $128.0 million available under the Sales Agreement.

~~11. Net Loss Per Share Attributable to Common Stockholders~~23

Share Repurchase Program

On April 10, 2025, the Company’s Board of Directors authorized a share repurchase program under which the Company may purchase up to $1.0 million of its outstanding Common Stock. Under the program, CDT may repurchase shares from time to time through open market transactions or other methods in compliance with SEC Rule 10b-18. Purchases will be executed by The Benchmark Company, the Company’s appointed broker, and will be subject to market conditions, corporate liquidity requirements, regulatory considerations, and other factors. As of June 30, 2025, the Company has repurchased an aggregate of 11,713 shares of its outstanding Common Stock at an average price of $8.85/share and paid approximately $2,000 in commission to the broker. The repurchased shares are recorded as treasury stock within the condensed consolidated balance sheets.

10. Net Loss Per Share Attributable to Common Stockholders

Potentially dilutive securities (upon conversion) that were not included in the diluted per share calculations because they would have been anti-dilutive were as follows:

	As of March 31,		As of March 31,
	As of June 30,		As of June 30,
	2025		2024
Public warrants		~~139~~9,~~790~~319		~~139~~9,~~790~~319
PIPE Warrants		-		~~200~~1,~~000~~333
A.G.P. Warrants		~~540~~36		~~540~~36
Convertible Promissory Notes Payable		-		~~805~~54
Stock Options		654,~~090~~030		~~10,717~~714
Restricted stock Units		-		1,470
A.G.P. Convertible Note		144,016		-
A.G.P. Convertible Note		1,816,695		-
March 2024 Warrants		173		173
March 2024 Warrants		2,600		2,600
April 2024 Warrants		965		965
April 2024 Warrants		14,477		-
A.G.P. 2024 Warrants		1,908		-
A.G.P. 2024 Warrants		28,626		-
Antidilutive Securities		160,447		12,594
Antidilutive Securities		2,067,818		355,922

2211. Related Party Transactions

12. Related Party Transactions

Corvus Capital Limited

Corvus Capital Limited (“Corvus”) is a significant investor in the Company through subscribing to 1,000 common shares prior to the closing of the Merger on September 22, 2023. Shares held by Corvus on the closing date of the Merger were exchanged for shares of the Company’s Common Stock. The Chief Executive Officer and principal owner of Corvus, Dr. Andrew Regan, is a member of ~~Conduit’s~~the ~~board~~Board ~~of directors~~ and was appointed as the Chief Executive Officer of the Company on April 15, 2025. Dr. Regan has not entered into any compensation plans and will continue to waive all compensation fees in connection with his service as Chief Executive Officer of the Company, and is entitled to reimbursement of expenses incurred in connection with his role as Chief Executive Officer.

For the three months ended ~~March~~June 3130, 2025 and 2024, the Company incurred director travel expenses payable to Dr. Regan of approximately $0.13 million and $0.2 million, respectively. For the six months ended June 30, 2025 and 2024, the Company incurred director travel expenses payable to Dr. Regan of approximately $0.3 million and $0.3 million, respectively. As of ~~March~~June 3130, 2025, and December 31, 2024, the Company did not owe Dr. Regan any director’s fees, as Dr. Regan and the Company agreed to cease director’s fees effective at the closing of the Merger.

In September 2023, concurrently with the completion of the Merger, pursuant to the PIPE Subscription Agreement (the “PIPE Subscription Agreement “) for an aggregate purchase price of $20.0 million, the Company issued an aggregate of 201,~~000~~333 shares of the Company’s Common Stock and PIPE Warrants (the “PIPE Warrants”) to purchase 201,~~000~~333 shares of Company Common Stock. At the time of the execution of the PIPE Subscription Agreement, Corvus and its affiliates entered into a participation and inducement agreement with Nirland whereby Corvus agreed to provide certain payments and economic benefits to Nirland. In certain circumstances, Nirland may have a right to cause Corvus to transfer ~~300~~20,~~484~~032 shares held by Corvus to Nirland.

Nirland

On August 6, 2024, the Company entered into the August 2024 Nirland Note with Nirland, a related party of the Company. The Company determined that Nirland was a related party due to Nirland’s ownership interest in the Company concurrently with the execution of the August 2024 Nirland Note. Additionally, on October 28, 2024, the Company issued the October 2024 Nirland Note to Nirland, and on October 31, 2024, the Company and Nirland amended the August 2024 Nirland Note, and on November 22, 2024, the Company and Nirland amended the August 2024 Nirland Note for a second time. As of ~~March~~June 3130, 2025, no obligations remained under the terms of the August 2024 Nirland Note and October 2024 Nirland Note, and Nirland did not own or beneficially own shares of the Company’s ~~common~~Common ~~stock~~Stock. Refer to Note 4 and Note 5 for additional information.

SARBORG

On December 12, 2024, and March 31, 2025, the Company entered into the Sarborg Service Agreement and the Sarborg Additional Agreement, respectively. Dr. Andrew Regan, Chief Executive Officer and member of ~~Conduit’s~~the ~~board of directors~~Board, also sits on the board of directors of Sarborg but does not have an equity interest in Sarborg. ~~During~~On ~~the~~January ~~three months ended March 31~~17, 2025, the Company ~~recorded~~issued $1,515 shares of fully vested unregistered Common Stock as an initial fee for the Sarborg Services Agreement.1 The fair value of the shares issued was $0.2 million and was recorded as ~~research~~a prepaid within the condensed consolidated balance sheets. The shares are being amortized over the ~~and~~initial ~~development~~12 ~~expense~~month ~~related~~term toof the Sarborg Service Agreement. ~~Additionally,~~to onresearch and development expense. On March 31, 2025, the Company issued 1123,~~853,933~~ 595 fully vested unregistered shares of Common Stock to prepay the Sarborg Additional Agreement. The fair value of the shares issued was $1.5 million and was recorded as a prepaid within the condensed consolidated balance sheets. During the three and six months ended June 30, 2025, the Company recorded $0.7 million and $1.5 million as research and development expense related to the Sarborg Service Agreement, respectively. During the three and six months ended June 30, 2025, the Company recorded $0.8 million as research and development expense related to the Sarborg Additional Agreement. Refer to Note 76 above for additional information.

Officers and Directors

On April 22, 2024, the Company issued in a private placement ~~common~~Common ~~stock~~Stock purchase warrants (the “April Warrants”) to third parties which also included certain directors, to purchase up to an aggregate of ~~9,077~~ 605 shares of the Company’s ~~common~~Common ~~stock~~Stock, in exchange for entering into a lock-up with respect to the shares of ~~common~~Common ~~stock~~Stock held by such holder and for such directors, an additional $12187.50 per warrant. The April Warrants are not exercisable until one year after their date of issuance. Each April Warrant is exercisable ~~into~~ into one share of the Company’s ~~common~~Common ~~stock~~Stock at a price per share of $~~312~~ 4,680 (as adjusted from time to time in accordance with the terms thereof) for a two-year period after the date of exercisability.

23Manoira

~~13.~~On ~~Other~~June ~~Income~~3, 2025, the Company entered into a joint development agreement (~~expense~~the “Joint Development Agreement”) with Manoira Corporation. Dr. Andrew Regan, ~~net~~Chief Executive Officer and member of the Board, also is a director and controlling member of Manoira. Chele Farley, a member of the Board, is Manoira’s sole director. Through the Joint Development Agreement, the Company and Manoira intend to jointly evaluate AZD1656, and any of its derivatives, as well as AZD5658, in animal health indications and produce transitional data to inform the Company’s human clinical programs while exploring veterinary market opportunities. The Company delivered shares of the Company’s Common Stock worth $0.5 million to Manoira as its contribution to the Joint Development Agreement, with Manoira bearing all subsequent costs incurred during the joint development period. During the three and six months ended June 30, 2025, the Company recorded a $0.4 million prepaid expense related to the Joint Development Agreement. Refer to Note 6 for additional details.

~~The following table presents other income (expense), net, for the three months ended March 31, 2025 and 2024 (in thousands):~~25

12. Other Expense, net

The following table presents other income (expense), net, for the three and six months ended June 30, 2025 and 2024 (in thousands):

Schedule of Other Expense, Net

	2025			2024
	For the three months ended June 30,						For the six months ended June 30,
	For the three months ended March 31,
	2025			2024			2025			2024
	2025			2024
Other income:
Other income:
Unrealized foreign currency transaction gain	$	4		$	-		$	27		$	-
Unrealized foreign currency transaction gain	$	26		$	-
Gain on change in fair value of derivative warrant liability		7			91			137			110
Gain on change in fair value of the warrants		130			19
Interest income		4			2			12			11
Gain on the change in fair value of convertible notes payable		204			-
Gain on debt extinguishment		-						278			-
Interest income		8			9
Gain on waiver of accrued interest		-						371			-
Gain on debt extinguishment		274			-
Gain on the issuance of shares for services		-			-			70			-
Gain on waiver of accrued interest		371			-
Total other income:		15			93			895			121
Gain on the issuance of shares for services		70			-
Other expense:
Total other income:		1,083			28
Loss on the change in fair value of convertible notes payable		1,034			-			2,875			-
Other expense:
Interest expense		57			119			233			238
Loss on the change in fair value of convertible notes payable		2,044			-
Loss on issuance of warrants for lock-up		-			2,208			-			2,710
Interest expense		176			119
Unrealized foreign currency transaction loss		-			7			-			11
Loss on issuance of warrants		-			502
Other		-			2						2
Unrealized foreign currency transaction loss		-			4
Total other expense		1,091			2,336			3,108			2961
Total other expense		2,220			625
Total other expense, net	$	(1,076	)	$	(2,243	)	$	(2,213	)	$	(2,840	)
Total other expense, net	$	(1,137	)	$	(597	)

~~14. Warrants~~26

13. Warrants

Equity Classified Warrants

The Publicly Traded Warrants, Private Placement Warrants, March 2024 Warrants, and the April 2024 Warrants (collectively the “Equity Classified Warrants”), are classified within permanent equity on the condensed consolidated balance sheets, as the settlement amount would equal the difference between the fair value of a fixed number of shares and a fixed monetary amount (or a fixed amount of a debt instrument).

Publicly Traded and Private Placement Warrants

Pursuant to MURF’s initial public offering, the Company sold ~~132~~8,~~250~~817 units at a price of $115,000 per unit. Each unit consisted of one share of MURF Class A common stock and one redeemable warrant “the “Publicly Traded Warrant”). Each whole Publicly Traded Warrant entitled the holder to purchase one share of Class A common stock at a price of $117,~~150~~250 per share, subject to adjustment. The warrants are publicly traded on The Nasdaq Capital Market under the trading symbol “CDTTW”.

Simultaneously with the closing of its initial public offering, MURF consummated the private sale to the Sponsor of ~~7,540~~503 private placement units at a a price of $115,000 per private placement unit. Each private placement unit was comprised of one share of MURF Class A common stock and one warrant (the “Private Placement Warrant”). Each Private Placement Warrant was exercisable to purchase one share of MURF Class A common stock at a price of $117,~~150~~250 per share, subject to adjustment. The private placement units (including the Class A common stock issuable upon exercise of the warrants included in the private placement units) were not transferable, assignable, or saleable until 30 days after the completion of a Merger, subject to certain exceptions.

Upon the closing of the Merger, the Company assumed the Publicly Traded Warrants and Private Placement Warrant. The Publicly Traded Warrant and Private Placement Warrant were amended to entitle each holder to purchase one share of the Company’s Common Stock.

March 2024 Warrants

On March 20, 2024, the Company issued in a private placement equity classified ~~common~~Common ~~stock~~Stock purchase warrants (the “March 2024 Warrants”) to an investor to purchase up to an aggregate ~~2,600~~173 shares of the Company’s Common Stock, in exchange for entering into a lock-up with respect to the shares of ~~common~~Common ~~stock~~Stock held by such holder (the “March Lock-Up Agreement”). The Company recognized at $0.5 million loss on the issuance of the warrants during the ~~three~~six months ended ~~March~~June 3130, 2024. The Company determined that the March 2024 Warrants should be classified within equity and estimated the fair value of the warrants issued as of March 20, 2024, using a Black-Scholes option-pricing model utilizing the following assumptions:

	March 20, 2024
Closing stock price	$	~~347~~5,205
Contractual exercise price	$	~~318~~4,770
Risk-free rate		4.41	%
Estimated volatility		78.5	%
Time period to expiration		3 Years

A fair value of $0.5 million was calculated and recorded within additional paid-in capital on the condensed consolidated balance sheets. The March 2024 Warrants are not exercisable until one year after their date of issuance. Each March 2024 Warrant is exercisable into one share of the Company’s Common Stock at a price per share of $~~318~~4,770 (as adjusted from time to time in accordance with the terms thereof) for a two-year period after the date of exercisability. There is no established public trading market for the March 2024 Warrants. Notwithstanding the foregoing, the March 2024 Warrants shall vest, and not be subject to forfeiture, with respect to 25% of such March 2024 Warrants commencing on the 90th day after the date of the March Lock-Up Agreement and 25% on each subsequent 90-day anniversary, in each case vesting only if the holder agrees to continue to have its shares of ~~common~~Common ~~stock~~Stock remain locked up pursuant to the March Lock-Up Agreement on such date.

April 2024 Warrants

On April 20, 2024, the Company issued in a private placement equity classified ~~common~~Common ~~stock~~Stock purchase warrants (the “April 2024 Warrants”) to shareholders’ of the Company to purchase up to an aggregate ~~14,477~~965 shares of the Company’s Common Stock, in exchange for (1) $12187.50 per warrant, and (2) entering into a lock-up with respect to the shares of ~~common~~Common ~~stock~~Stock held by such holders (the “April Lock-Up Agreement”). ~~9,077~~605 of the total April 2024 Warrants issued were issued to directors, related parties and management of ~~the~~ the Company. The Company determined that the April 2024 Warrants should be classified within equity and estimated the fair value of the ~~warrants~~ warrants as of April 20, 2024, using a Black-Scholes option-pricing model utilizing the following assumptions:

	April 20, 2024
Closing stock price	$	~~308~~4,620
Contractual exercise price	$	~~312~~4,680
Risk-free rate		4.81	%
Estimated volatility		78.3	%
Time period to expiration		3 Years

A fair value of $2.4 million was calculated and recorded within additional paid-in capital on the condensed consolidated balance sheets. The April 2024 Warrants are not exercisable until one year after their date of issuance. Each April 2024 Warrant is exercisable into one share of the Company’s Common Stock at a price per share of $~~312~~4,680 (as adjusted from time to time in accordance with the terms thereof) for a two-year period after the date of exercisability. There is no established public trading market for the April 2024 Warrants. Notwithstanding the foregoing, the April 2024 Warrants shall vest, and not be subject to forfeiture, with respect to 25% of such ~~March~~April 2024 Warrants commencing on the 90th day after the date of the April Lock-Up Agreement and 25% on each subsequent 90-day anniversary, in each case vesting only if the holder agrees to continue to have its shares of ~~common~~Common ~~stock~~Stock remain locked up pursuant to the April Lock-Up Agreement on such date.

Liability Classified Warrants

The PIPE Warrants, A.G.P. Warrants, and the A.G.P 2024 Warrants (collectively the “Liability Classified Warrants”), are classified as derivative liabilities because they do not meet the criteria in ASC 815-40 to be considered indexed to the entity’s own stock as the warrants could be settled for an amount that is not equal to the difference between the fair value of a fixed number of the entity’s shares and a fixed monetary amount. The Liability Classified Warrants are initially measured at fair value and are remeasured at fair value at subsequent financial reporting period end dates and upon exercise (see Note 3 for additional information regarding fair value).

For the three months ended ~~March~~June 3130, 2025 and ~~March 31,~~ 2024, the Company remeasured the fair value of the Liability Classified Warrants and recorded a gain on the change in the fair value of $6,000 and $0.1 million, respectively. For the six months ended June 30, 2025 and ~~$19~~2024,~~000, respectively~~ the Company remeasured the fair value of the Liability Classified Warrants and recorded a gain on the change in the fair value of $0.1 million in each period. The gains were recorded to other income (expense), net, on the condensed consolidated statements of operations and comprehensive loss. As of ~~March~~June 3130, 2025 and December 31, 2024, the condensed consolidated balance sheets contained warrant liabilities of $81,000 and $0.1 million, respectively.

PIPE Warrants and A.G.P. Warrants

Upon closing of the Merger, 201,~~000~~333 PIPE Warrants were issued to the PIPE Investors pursuant to subscription agreements. The warrants provide the PIPE Investors the right to purchase up to 201,~~000~~333 shares of Common Stock at an exercise price of $117,~~150~~250. Additionally, on the Closing Date of the Merger, the Company issued ~~540~~36 A.G.P. Warrants to an advisor for services provided directly related to the Merger. The warrants provide the advisor the right to purchase up to ~~540~~36 shares of Common Stock at an exercise price of $116,~~100~~500 per share.

The warrants issued to the PIPE Investors and the advisor contain materially the same terms and are exercisable for a period of five years, beginning on October 22, 2023.

On December 11, 2024, the Company reduced the exercise price of the PIPE Warrants to be $8132.8345, at which time all PIPE Warrants were exercised. The Company received approximately $0.2 million of proceeds from the exercise of the Warrants, all of which was used to pay down the October 2024 Nirland Note. As of ~~March~~June 3130, 2025, there are no outstanding PIPE Warrants.

A.G.P. 2024 Warrants

As partial consideration for an advance issued to the Company by A.G.P. on October 29, 2024, the Company issued A.G.P. Warrants (the “A.G.P. 2024 Warrants”) to purchase up to 281,~~625~~908 shares of the Company’s Common Stock at an exercise price of $10157.4820 per share. The Company determined that the A.G.P. 2024 Warrants should be classified as a liability and recorded at fair value through use of a Black-Scholes option-pricing model. Refer to Note 3 ~~above~~ for additional information.

2614. Commitments and Contingencies

15. Commitments and Contingencies

Legal Proceedings

The Company is subject to certain claims and contingent liabilities that arise in the normal course of business. While we do not expect that the ultimate resolution of any of these pending actions will have a material effect on our consolidated results of operations, financial position or cash flows, litigation is subject to inherent uncertainties. As such, there can be no assurance that any pending legal action, does not become material in the future. As of June 30, 2025, a contingency of $0.4 million is considered probable and reasonably estimable in relation to the Company’s legal proceedings. As such, the Company accrued an estimated liability in the accompanying financial statements.

In August 2023, prior to the Business Combination, our now wholly-owned subsidiary, Conduit Pharmaceuticals Limited, received a letter from Strand Hanson Limited (“Strand”) claiming it was owed advisory fees pursuant to a previously executed letter. ~~Conduit~~CDT rejected the claim from Strand and disputed the substance of the letter in full. Following such rejection, on September 7, 2023, Strand filed a claim in the Business and Property Courts of England and Wales claiming it is entitled to be paid the sum of $2 million and, as a result of the completion of the Business Combination, to be issued 654,~~000~~ 333 shares of ~~common~~Common ~~stock~~Stock. As of March 31, 2025, a potential contingency of $0.4 million is considered probable and reasonably estimable and as such, the Company accrued an estimated liability in the accompanying financial statements. The trial in this matter remains scheduled for October 20, 2025. We intend to vigorously defend against these claims. Regardless of its outcome, the litigation may impact our business due to, among other things, legal costs and the diversion of the attention of our management.

In November and December 2024, the Company received a letter from St George Street Capital and formal complaints filed with the Intellectual Property Office claiming the Company was assigned the US Application, and was not the sole owner, of the AZD 1656 co-crystal patent. In January 2025, ~~Conduit~~CDT issued a counter statement to the Intellectual Property Office disputing the claim filed by St George Street Capital. As of ~~March~~June 3130, 2025, the range of possible loss cannot be estimated and is not considered probable. As such, the Company has not accrued a loss contingency in the accompanying financial statements. We intend to vigorously defend against these claims. Regardless of its outcome, the litigation may impact our business due to, among other things, legal costs and the diversion of the attention of our management.

Leases

The Company has a lease agreement with respect to approximately 2,100 square feet of space in Cambridge, England, for a lease term ~~commencing in~~from March 2024 ~~and~~to ~~ending in~~ January 2027. As of ~~March~~June 3130, 2025, the Company has a right-of-use asset of $0.2 million and corresponding lease liability of $0.2 million recorded on the condensed consolidated balance sheets. Of the $0.2 million lease liability, $0.1 million is classified as short-term and $~~0.1~~46,000 ~~million~~ is classified as long-term. As of June 30, 2025, the Company has $0.2 million in future minimum lease payments remaining.

~~16. Segments~~29

~~The Company has one operating segment focused on the research and development of clinical assets~~15. ~~The accounting policies of the single operating~~ segment are identical to those described in Note 1. The CODM, which the Company has identified as Andrew Regan, Chief Executive Officer, manages the Company’s operations on a consolidated basis, assesses performance for the operating segment and decides how to allocate resources based on consolidated net loss, which is reported on the condensed consolidated statements of operations and comprehensive loss. Depreciation expense, amortization expense, stock-based compensation expense, and non-cash lease expense are significant noncash items included in consolidated net loss reviewed by the CODM and are reported on the consolidated statements of cash flows. The measure of segment assets is reported on the consolidated balance sheets as total consolidated assets. Expenditures for additions to long-lived assets, which include purchases of property and equipment, are included in total consolidated assets reviewed by the chief operating decision maker and are reported on the consolidated statements of cash flows.Segments

The Company has one operating segment focused on the research and development of clinical assets. The accounting policies of the single operating segment are identical to those described in Note 1. The Chief Operating Decision Maker (“CODM”), which the Company has identified as Dr. Andrew Regan, Chief Executive Officer, manages the Company’s operations on a consolidated basis, assesses performance for the operating segment and decides how to allocate resources based on consolidated net loss, which is reported on the condensed consolidated statements of operations and comprehensive loss. Depreciation expense, amortization expense, stock-based compensation expense, and non-cash lease expense are significant noncash items included in consolidated net loss reviewed by the CODM and are reported on the consolidated statements of cash flows. The measure of segment assets is reported on the consolidated balance sheets as total consolidated assets. Expenditures for additions to long-lived assets, which include purchases of property and equipment, are included in total consolidated assets reviewed by the chief operating decision maker and are reported on the consolidated statements of cash flows.

The CODM uses consolidated net loss and budget-to-actual variances to assess the performance of the operating segment and determine if the Company is progressing towards its goals.

The following table presents certain financial data for the Company’s reportable segment (in thousands):

	2025			2024
	Three Months ended June 30,						Six Months ended June 30,
	March 31,
(Dollar amounts in thousands)	2025			2024			2025			2024
	2025			2024
Operating expenses:
Research & development expense – clinical asset development	$	189		$	128
Research & development expenses-clinical asset development	$	222		$	25		$	411		$	153
Research & development expense – related parties		1,~~120~~638			-			2,365			-
General and administrative expenses – legal & professional fees		~~760~~872			~~245~~711			1,632			956
General and administrative expenses – accounting & audit fees		~~544~~378			~~647~~256			922			903
General and administrative expenses – salaries, payroll and stock-based compensation		693			986
General and administrative expenses – salaries, payroll and SBC		751			1,184			1,444			2,170
General and administrative expenses – other		703			949
General and administrative expenses - other		1,091			964			1,794			1,913
Loss from segment operations	$	4,009		$	2,955
Total operating costs and expenses		4,952			3,140			8,568			6,095
Operating loss		(4,952	)		(3,140	)		(8,568	)		(6,095	)
Other income (expenses):
Other income (expense), net		(1,023	)		(2,126	)		(1,992	)		(2,613	)
Interest Income		4			2			12			11
Interest expense, net		(57	)		(119	)		(233	)		(238	)
Total other (expense) income, net		(1,076	)		(2,243	)		(2,213	)		(2,840	)
Net loss	$	(6,028	)	$	(5,383	)	$	(10,781	)		(8,935	)

Other segment items consist of the items within Note 1312 to the condensed consolidated financial statements.

1716. Subsequent Events

~~Share~~Sarborg ~~Repurchase~~- ~~Program~~Additional Agreement Addendum

On ~~April~~July 101, 2025, the Company’s ~~Board~~entered ofinto ~~Directors~~an ~~authorized~~Addendum ato ~~share~~the ~~repurchase~~Additional ~~program~~Agreement ~~under~~with ~~which~~Sarborg ~~the~~Limited, ~~Company~~a ~~may~~related ~~purchase~~party. ~~up to~~Under ~~$1.0~~the ~~million~~terms of ~~its~~the ~~outstanding~~Addendum, ~~common~~Sarborg ~~stock.~~will ~~Under~~expand the ~~program,~~scope ~~Conduit~~of ~~may~~the ~~repurchase~~Additional ~~shares~~Agreement ~~from time~~ to ~~time~~provide ~~through~~external ~~open~~analysis ~~market~~of ~~transactions~~third-party pharma orcompanies ~~other~~assets ~~methods~~suitable infor ~~compliance~~drug ~~with SEC Rule 10b~~re-~~18.~~purposing ~~Purchases~~and ~~will~~evaluate bethe ~~executed~~efficacy byof ~~The~~the ~~Benchmark~~assets ~~Company,~~utilizing ~~the Company~~Conduit’s ~~appointed~~license to ~~broker,~~Sarborg’s ~~and~~machine ~~will~~learning beplatform. ~~subject~~The toscope ~~market~~of ~~conditions,~~work ~~corporate~~is ~~liquidity~~expected ~~requirements,~~to ~~regulatory~~be ~~considerations~~completed in 4 weeks, ~~and~~which ~~other~~may ~~factors.~~be Asrenewed or ofextended upon the ~~date~~mutual written agreement of ~~this~~the ~~Quarterly~~Parties. ~~Report~~The ontotal ~~Form~~consideration ~~10-Q,~~for the ~~Company~~additional ~~has~~services, ~~repurchased~~payable anin ~~aggregate~~cash ofin two ~~175~~tranches,~~694~~ ~~shares~~was of$0.3 ~~its outstanding common~~million. ~~stock~~The atCompany anpaid ~~average~~the ~~price~~full of $0.~~59/share~~3 ~~and~~million as ~~paid~~of ~~approximately~~the ~~$2,000~~date inof ~~commission~~this ~~to the broker~~filing.

~~Resignation~~Appointment of ~~David~~Permanent ~~Tapolczay~~Chief Financial Officer

OnEffective ~~April~~August 124, 2025 ~~(the “Effective Date”)~~, ~~Dr. David Tapolczay notified~~ the ~~Board of Directors (the “Board”) of~~ Company ofappointed ~~his~~James ~~resignation~~Bligh, ~~from~~co-founder, ~~both~~director ~~the Board~~ and ~~his~~Interim ~~position as~~ Chief ~~Executive~~Financial Officer ~~effective~~as ~~immediately. Dr. Tapolczay’s decision to resign was not~~ the ~~result~~permanent of any disagreement with the Company on any matter relating to the Company’s operations, policies, or practices. In connection with Dr. Tapolczay’s resignation, Dr. Tapolczay’s existing employment contract as Chief ~~Executive~~ Financial Officer ~~was terminated and Conduit UK Management LTD, a wholly owned subsidiary~~ of ~~the~~ ~~Company, entered into an Employment Agreement (~~the ~~“Employment Agreement”) with Dr~~Company. ~~Tapolczay pursuant to which Dr~~Mr. ~~Tapolczay~~ ~~will provide strategic advisory services as Head of Licensing & Strategy, reporting to the Chief Executive Officer. In exchange for Dr. Tapolczay~~Bligh’s ~~services,~~compensation he will ~~receive~~remain aunchanged ~~sign-on bonus of $129,000 (£100,000) base salary of $311,000 (£240,000). Consistent with the terms of the Company’s 2023 Stock Incentive Plan~~ and ~~subject to Dr. Tapolczay’s continued service pursuant to his Employment Agreement, his outstanding equity awards~~ he ~~has previously received~~ will ~~remain outstanding and~~ continue to ~~vest~~serve ~~based~~as ~~on the vesting dates thereof. Dr. Tapolczay will provide the Company with~~ a ~~release~~member of ~~claims~~the ~~and will be subject to certain non-competition, non-solicitation, non-disparagement, and confidentiality covenants~~Board.

~~Appointment~~Name ofChange ~~Andrew~~to ~~Regan~~CDT Equity Inc.

On ~~April~~August 155, 2025, the Company ~~appointed~~filed ~~Andrew~~a ~~Regan~~certificate asof ~~Chief~~amendment ~~Executive~~to ~~Officer,~~its ~~effective~~Second ~~immediately~~Amended ~~(the~~and ~~“Appointment”). As~~Restated aCertificate ~~result~~ of Incorporation (the ~~Appointment~~“Certificate of Incorporation”), ~~Dr.~~to ~~Regan~~effect ~~will~~a ~~serve~~change ~~as Chief Executive Officer~~ of the Company’s ~~and~~name ~~will~~from ~~continue~~“Conduit toPharmaceuticals ~~serve~~Inc.” asto ~~a director~~“CDT onEquity ~~the Board~~Inc.”, ~~Dr.~~which ~~Regan~~became ~~has~~effective ~~not~~at ~~entered~~5:00 ~~into~~P.M. ~~any~~Eastern ~~compensation~~Time ~~plans~~on ~~and~~August ~~will~~5, ~~continue~~2025. toThe ~~waive~~Company’s ~~all~~Common ~~compensation~~Stock ~~fees~~continues ~~in connection with~~to ~~his service as Chief Executive Officer and will~~ be ~~entitled~~listed toon ~~reimbursement~~The ofNasdaq ~~expenses~~Capital ~~incurred~~Market inunder ~~connection~~the ~~with~~ticker ~~his~~symbol ~~role~~“CDT”. asIn ~~Chief Executive Officer~~addition, ~~although~~ the ~~Board~~CUSIP ~~may~~number ~~assess~~for ~~this~~the ~~determination~~Common ~~from~~Stock remains ~~time~~the ~~to time~~same.

~~Resignation~~CDT ofEquity ~~Faith~~Inc. ~~Charles~~Amended and Restated 2023 Stock Incentive Plan

On August ~~April 16~~5, 2025, ~~Ms.~~at ~~Faith Charles~~the ~~notified~~Company’s ~~the~~2025 ~~Board~~Annual Meeting of ~~her~~Stockholders, ~~resignation~~stockholders ~~due~~approved toan ~~personal~~amendment ~~reasons,~~ and ~~resigned~~restatement asof athe Company’s ~~member~~2023 ofStock ~~the~~Incentive ~~Board~~Plan of(as amended, the ~~Company~~“Amended ~~and~~2023 ~~from~~Stock ~~all committees~~Incentive onPlan”) ~~which~~to ~~she~~authorize ~~served~~an additional 2,000,000 ~~effective~~shares ~~immediately.~~of ~~Ms.~~Common ~~Charles’s~~Stock ~~resignation~~for ~~was~~awards ~~not~~under ~~due~~the toAmended ~~any~~2023 ~~disagreement~~Stock ~~with~~Incentive ~~management~~Plan. The Amended 2023 Stock Incentive Plan was recommended orand approved by the ~~Company’s~~Board ~~operations,~~on ~~policies~~July or8, ~~practices~~2025.

~~Partial~~Sarborg ~~Conversion~~- ofAdditional ~~A.G.P.~~Agreement ~~Convertible~~Addendum ~~Note~~ 2

On ~~April~~August 11, 2025, ~~and April 16, 2025,~~ the ~~holder~~Company ofentered ~~the A.G.P. convertible note converted $0.5 million and $0.8 million of principal and interest~~ into ~~430,000~~Addendum ~~and~~2 ~~1,065,395~~to ~~shares of~~ the ~~Company’s~~Additional ~~common~~Agreement ~~stock,~~with ~~respectively.~~Sarborg ~~As of April 16~~Limited, ~~2025,~~a ~~the~~related ~~Company’s common stock price was trading below the Conversion Price Floor~~party. ~~For~~Under the ~~purpose~~ terms of ~~the~~Addendum ~~April 16~~2, ~~2025~~Sarborg ~~conversion,~~will ~~the~~expand ~~Company waived~~ the ~~Conversion~~scope ~~Price~~of ~~Floor~~work and ~~allowed~~integrate ~~A.G.P. to convert at~~ a ~~price~~Cryptocurrency ofAI ~~$0.78/share (the April 16~~Agent, ~~2025~~developed ~~closing~~specifically ~~stock~~for ~~price). As of the date of this Quarterly Report~~identifying, onforecasting ~~Form~~and ~~10-Q,~~recommending ~~approximately~~digital ~~$4.2~~currencies ~~million~~into inCDT ~~principal~~Equity’s ~~and~~Operations ~~interest~~as ~~remain~~part ~~outstanding~~of ~~under~~its ~~the~~Treasury AStrategy.~~G.P. Convertible Note.~~

28The Term of the Engagement is for a minimum of four (4) months, which may be renewed or extended upon the mutual written agreement of the Parties. The initial consideration for the Proposal for Expanded Scope of Work shall be $150,000, payable on execution of this Agreement. Conduit agrees to pay a further consideration of $150,000 in cash or shares (at CDT Equity’s sole discretion) at such time as CDT Equity invests more than $600,000 in cryptocurrency as part of its Treasury Strategy.

Sarborg is a related party, Dr. Andrew Regan, Chief Executive Officer and member of the Board, also sits on the board of directors of Sarborg but does not have an equity interest in Sarborg.

Item 2. Management’s Discussion and Analysis of Financial Condition and Results of Operations.

The following discussion and analysis of our financial condition and results of operations should be read in conjunction with the financial statements and the related notes included under Part I, Item 1 of this Quarterly Report on Form 10-Q (this “Quarterly Report”) as well as the Company’s audited financial statements and notes thereto included in its Annual Report on Form 10-K for the year ended December 31, 2024 that was filed with the SEC on March 28, 2025. Certain information contained in the discussion and analysis set forth below includes forward-looking statements that involve risks and uncertainties. The following discussion contains forward-looking statements based upon current expectations that involve risks, uncertainties and assumptions. Our actual results may differ materially from those anticipated in these forward-looking statements as a result of various factors, including those set forth under the section titled “Risk Factors” or in other parts of this Quarterly Report. Our historical results are not necessarily indicative of the results that may be expected for any period in the future. All dollar amounts are expressed in thousands of United States dollars (“$”), unless otherwise indicated.

Overview

On September 22, 2023, a merger transaction (the “Business Combination”) between Conduit Pharmaceuticals Limited (“Old Conduit”), Murphy Canyon Acquisition Corp (“MURF”) and Conduit Merger Sub, Inc., a Cayman Islands exempted company and a wholly owned subsidiary of MURF (“Merger Sub”), was completed pursuant to the Agreement and Plan of Merger, dated November 8, 2022, as amended, (the “Merger Agreement”). Pursuant to the terms of the Merger Agreement, at the closing, (i) Merger Sub merged with and into Old Conduit, with Old Conduit surviving the Business Combination as a wholly-owned subsidiary of MURF, and (ii) MURF changed its name from Murphy Canyon Acquisition Corp. to CDT Pharmaceuticals Inc. Effective August 5, 2025, the Company changed its name from Conduit Pharmaceuticals Inc. to CDT Equity Inc. Our change to CDT Equity Inc. reflects the evolution of our strategy as a data-driven biotech development company focused on identifying, enhancing, and advancing high-potential therapeutic assets through scientific innovation and strategic partnerships.

~~Conduit~~CDT ~~has~~Equity ~~developed~~is a ~~unique~~data-driven ~~business~~biotech ~~model~~development ~~that~~company ~~allows~~focused iton toidentifying, ~~act~~enhancing, asand aadvancing ~~conduit~~high-potential totherapeutic ~~bring clinical~~ assets through ~~from~~scientific ~~pharmaceutical~~innovation ~~companies~~ and ~~develop new~~strategic ~~treatments for patients~~partnerships. ~~Our~~The ~~novel~~company ~~approach~~has ~~addresses~~evolved ~~unmet~~into ~~medical~~a ~~needs~~broader, ~~and~~more ~~lengthens~~agile ~~the~~platform ~~intellectual~~that ~~property for our existing~~leverages ~~assets~~artificial ~~through~~intelligence, ~~cutting-edge~~ solid-form ~~technology~~chemistry, and ~~then~~efficient ~~commercializing~~asset ~~these~~repositioning ~~products~~to ~~with~~accelerate ~~life~~the ~~science~~development ~~companies.~~of ~~We continue to evaluate~~ novel ~~artificial~~therapeutic ~~intelligence and cybernetics approaches to drug re-purposing, intellectual property and asset selection to give Conduit a competitive advantage~~treatments.

~~We are led by highly experienced~~CDT ~~executives:~~Equity’s ~~Dr.~~strategy ~~Freda~~is ~~Lewis-Hall,~~centered ~~former~~on ~~Chief~~unlocking ~~Medical~~the ~~Officer~~untapped value of ~~Pfizer~~clinical-stage ~~Inc.~~compounds, ~~the~~particularly ~~Chair~~those ofdeprioritized ~~our~~by larger ~~Board~~pharmaceutical ofcompanies ~~Directors~~with strong, ~~and~~supporting ~~Dr.~~Phase ~~Andrew~~I ~~Regan~~safety data. ~~Our~~ ~~management~~Through ~~team~~advanced ~~includes~~co-crystallization ~~active~~and ~~senior~~solid-form ~~scientists~~technologies developed ~~who~~at ~~have~~our anCambridge ~~extensive understanding of the pharmaceuticals market~~facility, ~~which~~we ~~supports our~~aim ~~strategy~~to ofimprove ~~developing~~drug ~~clinical~~properties ~~assets~~and inhave asuccessfully ~~cost-efficient~~extended ~~manner~~patent ~~while~~life ~~focusing~~of oncertain ~~therapeutic~~drugs ~~efficacy~~by up ~~and~~to ~~patient~~20 ~~safety~~years.

~~Simultaneously,~~Our ~~Conduit~~current ~~leverages~~pipeline ~~the~~includes ~~capabilities~~candidates oftargeting ~~our~~inflammatory ~~Cambridge laboratory facility~~ and ~~highly~~autoimmune ~~experienced~~disorders, ~~team~~as ofwell ~~solid-form~~as ~~experts~~idiopathic tomale ~~extend~~infertility, ordermatology ~~develop proprietary solid-form intellectual property for our existing~~ and ~~future~~animal ~~clinical assets~~health. ~~Our~~The ~~own~~ intellectual property portfolio comprises pending patent applications in several international jurisdictions describing a solid-form compound, including the AZD1656 Cocrystal (a HK-4 Glucokinase Activator)~~, targeting a wide range of autoimmune disorders~~. Our pipeline research includes a number of ~~compounds~~ compounds that serve as promising alternatives to existing clinical assets currently marketed and sold by large pharmaceutical companies, ~~which~~ which we have identified as having an opportunity to develop further intellectual property positions through solid-form technology.

InOur ~~connection~~collaboration with ~~the~~Sarborg ~~funding~~enables ~~and~~us ~~development~~to ofapply ~~clinical~~proprietary ~~assets,~~algorithms weutilizing ~~expect~~AI-powered disease mapping to ~~evaluate~~identify ~~and~~novel ~~select~~re-purposing opportunities ~~the~~against ~~specific~~a ~~molecules~~database toof beover ~~developed~~800 disease signatures. Sarborg’s insights have directly informed two new combination ~~and~~patent ~~collaborate~~filings, ~~with~~strengthening ~~external~~our ~~CROs~~intellectual ~~and~~property ~~Key~~portfolio. ~~Opinion~~In ~~Leaders~~addition, ~~(“KOLs”)~~Equity tohas ~~run~~initiated pre-clinical ~~trials~~in-vitro ~~that~~models ~~are~~to explore ~~managed,~~new ~~funded~~indications, ~~and overseen~~guided by usAI-insights without human intervention. We ~~intend~~will toseek ~~leverage~~an ~~our~~exit ~~comprehensive~~through ~~clinical~~third-party ~~and~~license ~~scientific~~deals ~~expertise~~following successful in ~~order~~vitro toand ~~facilitate~~in ~~development~~vivo of pre-clinical ~~assets~~ ~~through~~trials, ~~Phase~~entering IIinto ~~trials~~agreements inwith anthird-parties ~~efficient~~to ~~manner~~pursue byfurther ~~using~~development, ~~CROs~~FDA approval, commercialization and ~~third-party~~marketing ~~service~~of ~~providers~~our assets . We ~~will~~continue ~~also~~to ~~collaborate~~evaluate ~~closely with~~novel ~~disease~~artificial ~~specific~~intelligence ~~KOLs~~and tocybernetics ~~collectively~~approaches ~~assess~~to ~~and~~drug re-purposing, ~~determine~~intellectual ~~the~~property ~~most~~and ~~appropriate~~asset ~~indications~~selection ~~for~~to ~~all~~give ~~our~~CDT ~~current~~a ~~and~~competitive ~~forthcoming assets~~advantage.

We believe that successful Phase II trials of the clinical assets in our pipeline will increase the value of our assets. There is no assurance that any clinical trials on the assets owned or licensed by us will be successful, however, following a successful Phase II clinical trial, we would look to licensing opportunities with large biotech or pharmaceutical companies, typically for up-front milestone payments and royalty income streams for the life of the asset patent. We anticipate using any future royalty income stream to develop our asset portfolio in combination with other potential sources of financing, including debt or equity financing.31

~~Outside~~The Sarborg ofAgreement, ~~our~~entered ~~proprietary~~into ~~owned~~between ~~patented~~the ~~clinical~~Company ~~assets,~~and ~~AstraZeneca~~Sarborg ~~agreed~~on toDecember ~~grant~~12, a2024 ~~license~~is designed to ~~the~~address ~~Company~~longstanding ~~under~~challenges ~~certain~~in ~~intellectual~~the ~~property~~pharmaceutical ~~rights~~sector, ~~controlled~~in particular by ~~AstraZeneca~~reducing ~~related~~human toerror ~~HK-4~~in ~~Glucokinase~~critical ~~activators~~decision-making ~~AZD1656~~processes ~~and AZD5658~~ in ~~all~~both ~~indications~~clinical development and ~~myeloperoxidase~~asset ~~inhibitor~~identification. ~~AZD5904~~By ~~for~~integrating ~~the~~Sarborg’s ~~treatment,~~algorithmic ~~prevention~~AI/cybernetics technology, ~~and~~CDT ~~prophylaxis~~aims ofto ~~idiopathic~~enhance ~~male~~efficiency, ~~infertility.~~lower ~~The~~costs, ~~Company~~and ~~will~~accelerate ~~be responsible for the development~~timelines ~~and~~by ~~commercialization~~minimizing ofhuman ~~the~~intervention, ~~Licensed~~ultimately ~~Products~~optimizing ~~under~~ the ~~related~~drug ~~License~~development ~~Agreement.~~cycle ~~The~~and ~~Company~~giving isCDT ~~required~~a tocompetitive ~~use~~advantage ~~commercially~~in ~~reasonable efforts to develop and commercialize~~ the ~~Licensed Products~~sector.

29Through this relationship, CDT will gain access to cutting-edge predictive models and dashboards, enabling the Company to evaluate drug candidates, streamline clinical trials, and optimize asset management with real-time data. These tools will drive faster, more accurate decisions, improving efficiency and reducing costs. By leveraging these insights, CDT can differentiate itself in a competitive sector and gain unique data-driven insights that position the Company for success across both its current and future asset portfolio.

~~AstraZeneca~~A further ~~has~~partnership ~~conducted~~with ~~initial~~Manoira ~~pre-clinical~~enables ~~and,~~CDT inEquity ~~some~~to ~~instances,~~expand ~~clinical~~the ~~trials~~scope onof ~~these~~its ~~assets,~~drug ~~but~~portfolio ~~has~~into ~~decided~~the toanimal ~~license~~health ~~them~~market ~~for~~in ~~further~~a cost-efficient ~~development~~manner. AsThis collaboration allows us to accelerate the ~~clinical~~understanding ~~assets~~of ~~have~~the ~~undergone~~mechanism ~~initial~~of ~~pre-clinical~~action, safety, and ~~clinical~~potential ~~testing~~efficacy ~~conducted~~of byits portfolio ~~AstraZeneca~~across multiple species, wewhile ~~are~~retaining ~~able~~100% ~~to use~~ownership ~~the~~of ~~safety~~all data and intellectual property generated inrelating ~~these~~for ~~clinical~~human ~~trials~~applications. This is expected to ~~assess~~enhance ~~which~~the ~~clinical~~core ~~assets~~human totherapeutic ~~further~~pipeline ~~develop~~but ~~and~~also ~~for~~opens ~~which~~potential ~~indications~~new revenue streams in the high-growth veterinary market.

~~Through~~Repositioning ~~this~~CDT ~~relationship,~~Equity ~~there~~enables ~~are~~the ~~considerable~~company ~~APIs~~to ~~that~~explore ~~were~~multiple ~~manufactured~~opportunities byin ~~AstraZeneca~~the ~~(prior~~healthcare, tobiotech ~~conducting~~and ~~its~~broader ~~clinical~~technology ~~trials)~~innovation. ~~available~~The Board continue to ~~Conduit.~~evaluate As a ~~result,~~cryptocurrency ~~Conduit~~treasury ~~may~~reserve ~~not~~strategy, ~~have~~working with consultants to ~~develop~~best ~~the~~advise ~~APIs,~~a ~~which~~novel ismarket ~~often~~which ahas ~~time~~seen significant ~~consuming~~recent activity and ~~expensive~~success ~~process,~~for ~~and~~respective ~~the~~stakeholders. ~~APIs~~Long-term exposure to digital assets can present both strategic and ~~already~~financial ~~produced~~benefits ~~were~~as ~~subject~~part toof ~~rigorous~~a ~~quality~~diversified ~~control~~capital ~~measures~~management approach.

~~In collaboration~~Operating with ~~SARBORG~~a ~~Limited~~lean, ~~(“Sarborg”)~~disease-agnostic model, aCDT ~~related~~Equity ~~party~~prioritizes speed, ~~Conduit~~adaptability, ~~intends~~and tocapital ~~leverage~~efficiency. anWe ~~advanced~~avoid AIthe ~~and~~cost ~~cybernetics~~burden of late-stage clinical trials, focusing ~~platform~~instead toon ~~evaluate~~high-leverage ~~key~~development ~~deliverables~~strategies. ~~across~~Led ~~multiple~~by ~~areas~~highly experienced executives: Dr. Freda Lewis-Hall, former Chief Medical Officer of Pfizer Inc., the ~~Company’s~~Chair ~~operations,~~of ~~including~~the ~~drug~~Board; ~~repurposing~~Dr. Andrew Regan, ~~drug~~CEO ~~discovery~~and James Bligh, CFO. Our management team includes active senior scientists ~~solid-form~~who ~~identification~~have an extensive understanding of the pharmaceuticals market, ~~and~~supporting our strategy of developing clinical ~~trial~~assets ~~monitoring~~in a cost-efficient manner focused on therapeutic efficacy.

~~The~~In ~~Sarborg~~2024, ~~Agreement~~AstraZeneca ~~entered~~granted a ~~into~~license ~~between~~to the Company ~~and~~under ~~Sarborg~~certain onintellectual ~~December~~property ~~12,~~rights ~~2024~~controlled ~~(the~~by ~~“Sarborg~~AstraZeneca ~~Agreement”)~~related ~~is designed~~ to ~~address~~HK-4 ~~longstanding~~Glucokinase ~~challenges~~activators AZD1656 inand ~~the~~AZD5658 ~~pharmaceutical sector,~~ in ~~particular~~all byindications ~~reducing~~and ~~human~~myeloperoxidase ~~error~~inhibitor inAZD5904 ~~critical~~for ~~decision-making~~the ~~processes~~treatment, inprevention, ~~both~~and ~~clinical~~prophylaxis ~~development and~~of ~~asset~~idiopathic ~~identification~~male infertility. ByThe ~~integrating~~Company ~~Sarborg’s~~will ~~algorithmic~~be ~~AI/cybernetics~~responsible ~~technology,~~for ~~Conduit~~development ~~aims~~and tocommercialization ~~enhance~~of ~~efficiency,~~the ~~lower costs,~~Licensed ~~and~~Products ~~accelerate~~under ~~timelines~~the byrelated ~~minimizing~~License Agreement. ~~human~~The ~~intervention,~~Company ~~ultimately~~is ~~optimizing~~required ~~the~~to ~~drug~~use ~~development~~commercially ~~cycle~~reasonable ~~and~~efforts ~~giving~~to ~~Conduit a~~develop ~~competitive~~and ~~advantage~~commercialize in the ~~sector~~Licensed Products.

~~Through this~~AstraZeneca ~~relationship,~~has ~~Conduit~~conducted ~~will gain access to cutting~~initial pre-~~edge~~clinical ~~predictive models~~ and ~~dashboards~~, ~~enabling~~in ~~the~~some ~~Company to evaluate drug candidates~~instances, ~~streamline~~ clinical trials, ~~and~~on ~~optimize~~these ~~asset~~assets, ~~management~~but ~~with~~has ~~real-time~~decided ~~data.~~to ~~These~~license ~~tools~~them ~~will~~for ~~drive~~further ~~faster,~~development. ~~more~~As ~~accurate decisions,~~the ~~improving~~clinical ~~efficiency~~assets ~~and~~have ~~reducing~~undergone ~~costs.~~initial Bypre-clinical ~~leveraging~~and ~~these~~clinical ~~insights,~~testing ~~Conduit~~conducted ~~can~~by ~~differentiate~~AstraZeneca, ~~itself~~we inare aable ~~competitive~~to ~~sector~~use ~~and~~the ~~gain unique~~safety data~~-driven~~ generated ~~insights~~in ~~that~~these ~~position~~clinical ~~the~~trials ~~Company~~to ~~for~~assess ~~success~~which ~~across~~clinical ~~both~~assets ~~its~~to ~~current~~further develop and ~~future asset portfolio~~re-purpose.

~~In addition~~Furthermore, ~~Conduit~~CDT ~~will~~is ~~retain~~well apositioned to ~~perpetual~~pursue, ~~non-exclusive, royalty-free,~~ and ~~assignable~~intends ~~right~~ to ~~use~~pursue, ~~any~~additional ~~platform~~relationships and/or ~~technology~~partnerships ~~developed by~~with ~~Sarborg~~third inparties ~~association~~for ~~with~~ the ~~deliverables.~~licensing ~~Ongoing~~of ~~support~~further ~~from~~assets which ~~Sarborg~~are ~~will~~currently ~~ensure~~deprioritized. ~~these~~We ~~systems~~plan ~~evolve~~to ~~with~~focus ~~Conduit’s~~our ~~needs, driving~~efforts ~~long-term~~on ~~innovation~~developing inclinical ~~areas~~assets ~~like~~to IPaddress ~~creation,~~disorders ~~regulatory~~that ~~strategy,~~impact ~~and~~a ~~clinical trial monitoring. This partnership reinforces~~large ~~Conduit’s~~population ~~commitment~~where tothere ~~leveraging~~is ~~AI-driven~~no ~~solutions~~present totreatment ~~accelerate~~or ~~growth,~~the ~~deliver~~present ~~value to shareholders~~treatment, ~~and~~carries ~~maintain~~significant aunwanted ~~competitive edge~~side ~~in the pharmaceutical sector~~effects.

This strategic move reaffirms Conduit’s commitment to adopting forward-thinking solutions to stay at the forefront of innovation in the pharmaceutical industry. By reducing reliance on traditional, labor-intensive methods and harnessing the power of AI-driven technology, Conduit is well-positioned to lead in areas such as drug repurposing, clinical trial monitoring, and IP creation, ensuring the Company’s long-term growth and market leadership.32

Furthermore, Conduit is well positioned to pursue, and intends to pursue, additional relationships and/or partnerships with third parties for the licensing of further assets which are currently deprioritized. We plan to focus our efforts on developing clinical assets to address disorders that impact a large population where there is no present treatment or the present treatment, carries significant unwanted side effects.

Key Component of Result of Operations

Operating Expenses

Research and Development Expenses

Research and development expenses consist primarily of costs incurred in connection with the research and development of our candidates and programs. We expense research and development costs and intangible assets acquired that have no alternative future use as incurred. These expenses include:

	●	personnel-related expenses, including salaries, bonuses, benefits and stock-based compensation for employees engaged in research and development functions;

	●	expenses incurred in connection with the clinical development and regulatory approval of our clinical assets, including under agreements with third parties, such as consultants, contractors and CROs;

	●	license fees with no alternative use; and

	●	other expenses related to research and development.

We expense research and development costs with no alternative future use as incurred. Advance payments that we make for goods or services to be received in the future for use in research and development activities are recorded as prepaid expenses. The prepaid amounts are expensed as the benefits are consumed.

We incurred approximately $1.38 million and $25,000 on research and development activities during the three months ended June 30, 2025, and June 30, 2024, respectively. We incurred approximately $2.8 million and $0.12 million on research and development activities during the ~~three~~six months ended ~~March~~June 3130, 2025, and ~~March~~June 3130, 2024, respectively. Our research and development activities have been ~~wholly~~ focused on developing co-crystals of AZD1656 to increase patent life as well as purchasing technology to help us determine the feasibility that AZD1656, and potentially other de-prioritized assets, reaches commercialization. Some of this work was completed by third-party CROs but all intellectual property is retained by us. We currently have one pending international patent application and two pending national patent applications. The successful completion of clinical trials increases the value of clinical assets and may lead to the commercialization and/or licensing of such assets to other pharmaceutical companies. There is no assurance that any clinical trials on the assets owned or licensed by us will be successful.

General and Administrative Expenses

General and administrative expenses consist of salaries and other related costs, legal fees relating to intellectual property and corporate matters, professional fees for accounting, auditing, tax and consulting services, insurance costs, travel, and other operating costs.

We anticipate that our general and administrative expenses will increase substantially for the foreseeable future as we increase our administrative headcount to operate as a public company and as we advance clinical assets through clinical development. We also will incur additional expenses as a result of operating as a public company, including expenses related to compliance with the rules and regulations of the SEC and the Nasdaq listing rules, additional insurance expenses, investor relations activities and other administrative and professional services. In addition, if regulatory approval is obtained for clinical assets, we expect to incur expenses associated with building a sales and marketing team.

Other Income (Expenses)

Other income (expenses), net

Other income (~~expense~~expenses), net consists of change in the fair value of options, change in fair value of convertible notes, and expense incurred upon the issuance of warrants during the year.

Interest expense, net

Interest expense, net consists primarily of interest expense on convertible loan notes and promissory notes and interest expense on deferred commissions payable to an advisor for fees related to the merger, as well as a small amount of interest income on cash and cash equivalents held by the Company.

Results of Operations

The following table set forth our results of operations for the periods indicated:

	Three Months ended March 31,
	Three Months ended June 30,						Six Months ended June 30,
(In thousands, except share and per share amounts)	2025			2024
(Dollar amounts in thousands)	2025			2024			2025			2024
Operating expenses:
Research and development expenses	$	1,~~309~~860		$	~~128~~25		$	2,776		$	153
General and administrative expenses		23,~~700~~092			23,~~827~~115			5,792			5,942
Total operating costs and expenses		4,~~009~~952			23,~~955~~140			8,568			6,095
Operating loss		(4,~~009~~952	)		(23,~~955~~140	)		(8,568	)		(6,095	)
Other income (expenses):
Other income (expense), net		(~~969~~1,023	)		(~~487~~2,126	)		(1,992	)		(2,613	)
Interest Income		84			92			12			11
Interest expense, net		(~~176~~57	)		(119	)		(233	)		(238	)
Total other (expense) income, net		(1,~~137~~076	)		(~~597~~2,243	)		(2,213	)		(2,840	)
Net loss	$	(56,~~146~~028	)	$	(35,~~552~~383	)	$	(10,781	)		(8,935	)

Comparison of the Three Months Ended ~~March~~June 3130, 2025 and 2024

Research and Development Expenses

Three Months ended March 31,

Change

Three Months ended June 30,

Change

(Dollar amounts in thousands)

2025

2024

Amount

Research and development expenses

1,~~309~~860

~~128~~25

1,~~181~~835

~~923~~7,340

Research and development expenses increased by $1.28 million, or ~~923~~7,340%, ~~to approximately $1.3 million~~ for the three months ended ~~March~~June 3130, 2025, as compared to $~~0.1~~25 ~~million~~ thousand for the three months ended ~~March~~June 3130, 2024. The increase was primarily due to $1.16 million of expense recorded under the Sarborg Service Agreement and Sarborg Additional Agreement and $0.1 million of expense ~~incurred~~recorded under the ~~Charles~~Thesprogen ~~River~~Agreement, ~~MSA~~and $0.1 million in other research and development related activity.

General and Administrative Expenses

	Three Months ended March 31,				Change
	Three Months ended June 30,				Change
(Dollar amounts in thousands)	2025		2024		Amount			%
General and administrative expenses	$	23,~~700~~092	$	23,~~827~~115	$	(~~127~~23	)		(41	)%

General and administrative expenses decreased by $~~0.1 million~~23,000, or ~~4%,~~approximately toone ~~$2.7~~percent, ~~million~~during ~~for~~ the three months ended ~~March 31~~June 30, 2025, as compared to ~~$2.8 million for~~ the three months ended ~~March~~June 3130, 2024. The decrease was ~~primarily~~ driven by a $0.34 million decrease in payroll ~~salaries~~ and stock-based compensation expense, partially offset by a $0.12 million ~~decrease~~increase in ~~travel~~legal ~~and other general and administrative expenses~~fees, a $0.1 million ~~decrease~~ increase in accounting and audit ~~expenses,~~expense and a $0.1 million ~~decrease~~increase in ~~insurance~~travel expense ~~related to the amortization of prepaid directors and officers insurance, partially offset by a $0~~.~~5 million increase in legal expenses.~~

3134

Other Income (Expense), Net

	Three Months ended March 31,						Change
	Three Months ended June 30,						Change
(Dollar amounts in thousands)	2025			2024			Amount			%
Other income (expense), net	$	(~~969~~1,023	)	$	(~~487~~2,126	)	$	(~~482~~1,103	)		99(52	)%

Other income (expense), net changed by $01.51 million, or 9952%, to $1.0 million of expense for the three months ended ~~March~~June 3130, 2025, as compared to $02.51 million of net expense for the three months ended ~~March~~June 3130, 2024. The ~~$1.0~~decrease ~~million~~was ~~in other income (expense) for the three months ended March 31, 2025 is~~ primarily ~~related~~driven toby a ~~$1.8~~decrease ~~million loss on the change in fair value~~ of ~~convertible notes, partially offset by a~~ $02.12 million ~~gain~~related onto the ~~change~~issuance of warrants in ~~fair~~exchange ~~value~~for ofstockholders’ ~~the~~entering ~~warrant~~into ~~liability,~~lock-up ~~$0.3~~agreements ~~million~~during ~~gain~~the onthree ~~debt~~months ~~extinguishment~~ended June 30, ~~and~~2024 ~~$0.4~~partially ~~million~~offset ~~gain~~by onan ~~the~~increase ~~waiver~~ of ~~accrued interest. The~~ $01.51 million in ~~other~~the ~~income~~loss ~~(expense)~~on ~~for~~ the ~~three~~change ~~months~~in ~~ended~~fair ~~March~~value ~~31,~~of ~~2024~~convertible ~~was~~notes ~~primarily related to a $0~~payable.~~5 million loss on the issuance of warrants.~~

For further details refer to Note 1312, “Other income (expense), net,” in the unaudited financial statements as of ~~March~~June 3130, 2025 and ~~March~~June 3130, 2024 included elsewhere in this ~~Quarterly Report~~document.

Interest Expense, Net

	Three Months ended March 31,						Change
	Three Months ended June 30,						Change
(Dollar amounts in thousands)	2025			2024			Amount			%
Interest expense, net	$	(~~176~~57	)	$	(119	)	$	(5762	)		48(52	)%

Interest expense, ~~was~~net decreased by $~~0.2~~62,000, ~~million~~or 52%, to $57,000 for the three months ended ~~March~~June 3130, 2025, as compared to $0.1 million for the three months ended ~~March~~June 3130, 2024. The change was driven by ~~$77,000~~a decrease of ~~interest expense on the A~~$0.~~G.P.~~1 ~~Convertible Note,~~million ~~$24,000~~ of interest expense on the ~~August~~deferred ~~2024~~commission ~~Nirland~~payable ~~Note,~~to ~~$8,000~~an ofadvisor ~~interest~~for ~~expense~~fees ~~on the October 2025 Nirland Note, and $65,000 of debt issuance cost amortization~~ related to the ~~Convertible Promissory Note Payable~~merger, ~~partially~~ offset by aan ~~$79,000~~increase ~~decrease~~ of ~~interest expense related to the Deferred Commission Payable balance and a~~ $4057,000 of ~~decrease of~~ interest expense on the A.G.P. Convertible ~~Promissory~~ Note ~~Payable~~.

Comparison of the Six Months Ended June 30, 2025 and 2024

Research and Development Expenses

Six Months ended

June 30,

Change

(Dollar amounts in thousands)

2025

2024

Amount

Research and development expenses

2,776

153

2,623

1,714

Research and development expenses increased by $2.6 million, or 1,714%, for the six months ended June 30, 2025, as compared to $0.2 million for the six months ended June 30, 2024. The increase was primarily due $2.4 million of expense recorded under the Sarborg Service Agreement and Sarborg Additional Agreement, $0.1 million of expense incurred under Thesprogen Consulting Agreement, and $0.1 million in other research and development related activities.

General and Administrative Expenses

Six Months ended

June 30,

Change

(Dollar amounts in thousands)

2025

2024

Amount

General and administrative expenses

5,792

5,942

(150

)

General and administrative expenses decreased by $0.15 million, or 3%, to $5.8 million for the six months ended June 30, 2025, as compared to $5.9 million for the six months ended June 30, 2024. The decrease was primarily driven by a $0.7 million decrease in salaries and stock compensation expense, a $0.1 million decrease in other general and administrative expenses and a $0.1 million decrease in insurance expense related to the amortization of prepaid directors and officers insurance, partially offset by a $0.7 million increase in legal expenses and a $0.1 increase in travel expense.

Other Income (Expense), Net

Six Months ended

June 30,

Change

(Dollar amounts in thousands)

2025

2024

Amount

Other income (expense), net

(1,992

)

(2,613

)

621

Other income (expense), net changed by $0.6 million, or 24%, to $2.0 million of expense for the six months ended June 30, 2025, as compared to $2.6 million of net expense for the six months ended June 30, 2024. The change in other income (expense) for the six months ended June 30, 2025 is primarily related to a $2.7 million decrease related to the issuance of warrants in exchange for stockholders’ entering into lock-up agreements during the six months ended June 30, 2024, a $0.4 million decrease related to a waiver of interest on the A.G.P. Convertible Note, and a $0.3 million gain on debt extinguishment, partially offset by a $2.9 million loss on the change in fair value of convertible notes payable.

For further details refer to Note 12, “Other income (expense), net,” in the unaudited financial statements as of June 30, 2025 and June 30, 2024 included elsewhere in this document.

Interest Expense, Net

Six Months ended

June 30,

Change

(Dollar amounts in thousands)

2025

2024

Amount

Interest expense, net

(233

)

(238

)

Interest expense, net increased by $5,000, or 2%, during the three months ended June 30, 2025, as compared to the three months ended June 30, 2024. The change was immaterial for the six months ended June 30, 2025 as compared to June 30, 2024.

Liquidity and Capital Resources

Management assesses liquidity in terms of our ability to generate cash to fund operating, investing and financing activities. Since our inception, and in line with our growth strategy, we have prepared our financial statements assuming we will continue as a going concern. Since our inception, we have incurred net losses and experienced negative cash flows from operations. To date, our primary sources of capital have been through convertible debt, private placements of equity securities and ~~convertible debt and~~ the Sales Agreement with A.G.P. During the ~~three~~six months ended June ~~March 31~~30, 2025 and 2024, we incurred operating losses of $58.16 million and $3.6.1 million, respectively.

Sources and Uses of Liquidity

Our primary ~~uses~~use of cash ~~are~~is to fund our operations as we continue to grow our business. We will require a significant amount of cash for ~~expenditures~~ expenditures as we invest in ongoing research and development and business operations. Until such time we can generate significant revenue from the successful approval and commercialization of a product candidate, we expect to finance our cash needs for ongoing research and ~~development~~ development and business operations through public or private equity or debt financings or other capital sources, including strategic partnerships. However, we may be unable to raise additional funds or enter into such other arrangements, when needed, on favorable terms or at all. To the extent that we raise additional capital through the sale of equity or convertible debt securities, the ownership interest of our stockholders will be, or could be, diluted, and the terms of these securities may include liquidation or other preferences that ~~adversely~~ adversely affect the rights of our common stockholders. Debt financing and equity financing, if available, may involve agreements that ~~include~~ include covenants, limiting or restricting our ability to take specific actions, such as incurring additional debt, making capital expenditures or declaring dividends. If we are unable to raise additional funds through equity or debt ~~financings~~financing when needed, we may be required to to delay, limit, or substantially reduce research and development efforts all of which could have a material adverse effect on the Company and its financial results.

While the Company believes in the viability of its ability to raise additional funds, there can be no assurances to that effect. We have based our estimates on assumptions of operating costs that may prove to be wrong. As a result, we could deplete our capital resources sooner than we currently expect. If, for any reason, our expenses differ materially from our assumptions or we utilize our cash more quickly than anticipated, or if we are unable to obtain funding on a timely basis we may be required to revise our business plan and strategy, which may result in significantly curtailing, delaying or discontinuing one or more of our research or development programs or the commercialization of any product candidates or may result in our being unable to expand our operations or otherwise capitalize on our business opportunities. As a result, our business, financial condition, and results of operations could be materially affected.

Management has concluded that there is substantial doubt regarding our ability to continue as a going concern for a period of at least 12 months from the date of the filing of this Quarterly Report. This is based on our analysis under applicable accounting principles. These financial statements have been prepared assuming the Company will continue as a going concern and do not include adjustments to reflect the possible effects on the recoverability and classification of assets or the amounts and classification of liabilities that may result from the outcome of this uncertainty.

Cash Requirements

Our material cash requirements include the following contractual and other obligations.

A.G.P Convertible Note

On November 25, 2024, the Company issued to A.G.P. a convertible promissory note (the “A.G.P. Convertible Note”) in the principal amount of $5.7 million to evidence A.G.P.’s currently owed deferred commission payable. Unless earlier converted as specified in the A.G.P. Convertible Note, the principal amount plus all accrued but unpaid interest is due on November 25, 2025 (the “Maturity Date”). The A.G.P. Convertible Note accrues interest at 5.5% per annum.

At any time prior to the full payment of the A.G.P. Convertible Note, provided that A.G.P. has given at least three business days written notice to the Company, A.G.P., in its sole discretion, may elect to have all or any portion of the outstanding principal amount and all interest accrued converted into shares of the Company’s ~~common~~Common ~~stock~~Stock, at the lower of the Reverse Split price and the market price per share at the time of the conversion date, but in no event less than $1.00, subject to adjustment as provided therein and to take into account any future share splits or reverse splits. However, the conversion of the A.G.P. Convertible Note may not occur prior to the Company having sufficiently authorized shares of ~~common~~Common ~~stock~~Stock to permit the entire conversion of the convertible promissory note. Refer to Note 4 to our financial statements included elsewhere in this Quarterly Report on Form 10-Q.

On March 31, 2025, April 11, 2025, April 16, 2025, June 2, 2025, June 17, 2025, and June 26, 2025, the holder of the A.G.P. ~~exercised~~convertible note ~~their~~converted ~~conversion~~$0.4 ~~option~~million, ~~and~~$0.5 ~~converted~~million, $0.48 million, $0.1 million, $0.2 million, and $0.2 million of principal and interest ~~for~~into 28,667, ~~430~~28,666, 71,026, 40,000, 90,000, and 100,000 shares of ~~common stock~~the Company’s Common Stock, respectively. As of ~~March~~June 3130, 2025, there was approximately $53.56 million ofin outstanding principal and interest ~~remained outstanding~~remaining.

Working Capital

We currently anticipate that cash required for working capital for the next 12 months is approximately $12.7 million, which includes forecasted research and development costs of $1.3 million, forecasted general and administrative costs of $7.2 million, and a convertible promissory note payable, if not converted prior to maturity of $4.2 million. We do anticipate being able to fund required working capital for the next 12 months with cash and cash equivalents on hand and current borrowings. Management believes that we will be able to fund cash required for the next 12 months through borrowings and equity raises. We have historically been able to access funds through the issuance of debt, and more recently the at the market offering program agreement, and believe we can continue to obtain funding through such debt financing agreements and Sales agreement as needed to meet cash requirements for the next 12 months.

As of ~~March~~June 3130, 2025, we had raised $1115.9 million ~~(net of fees)~~ out of the $23.9 million available to us through the Sales ~~agreement~~Agreement and expect to raise the additional $118.60 million ~~(net of fees)~~ over the next 12 months.

Cash Flows

The following table set forth our cash flows for the period indicated (in thousands):

	Three Months ended March 31,
	Six Months ended June 30,
	2025			2024
Net cash provided by (used in):
Net cash (used in) provided by:
Operating Activities	$	(46,~~329~~509	)	$	(23,~~357~~870	)
Investing Activities		(4405	)		-(224	)
Financing Activities		59,~~927~~684			-113
Effect of exchange rate changes on cash and cash equivalents		~~(18~~8	)		(2728	)
Net increase (decrease) in cash and cash equivalents	$	1,576		$	(2,384	)
Net increase(decrease) in cash and cash equivalents	$	2,778		$	(4,009	)

Cash Flows Used in Operating Activities

Net cash used in operating activities for the ~~three~~six months ended ~~March~~June 3130, 2025, was $46.35 million, resulting primarily from a net loss of $510.18 million, adjusted for non-cash items including a $10.84 million ~~loss~~ gain on ~~the~~waiver ~~change in fair value~~ of ~~convertible~~accrued ~~notes payable~~interest, a $0.3 million gain on debt extinguishment, $0.31 ~~million~~change ~~gain~~in onfair ~~waiver~~value of ~~accrued~~derivative ~~interest~~warrant liability, a $02.19 million ~~gain on~~ change in fair value of ~~warrant~~convertible ~~liability~~notes, $01.2 8 million of ~~stock-based~~amortization ~~compensation~~ expense, $0.24 million of ~~non~~stock-~~cash~~based ~~interest expense~~compensation, $0.2 million of ~~amortization~~non-cash interest expense, ~~$0.4 million of prepaid directors~~ and ~~officers insurance amortization and~~ a $10.62 million cash outflow from operating assets and liabilities. The $10.6 2 million cash outflow from operating assets and liabilities is primarily due to a $0.72 million cash outflow from accounts payable, a $0.2 1 million cash outflow from accrued expenses and other current liabilities, and a $0.31 million cash outflow from operating lease liabilities, partially offset by a $0.2 million cash inflow from prepaid expenses and other current assets.

Net cash used in operating activities for the ~~three~~six months ended ~~March~~June 3130, 2024, was $23.49 million, resulting primarily from a net loss of $8.9 million and a change in the fair value of warrants of $30.61 million, adjusted for non-cash items including $0.49 million of stock-based compensation, a $0.49 million of amortization expense, a $02.57 million expense on the issuance of warrants, ~~and a~~ $0.12 million interest expense of the deferred commission payable, $0.2 million non-cash share issuance and a $0.4 million cash inflow from operating assets and liabilities. The $0.24 million cash ~~outflow~~inflow from operating assets and liabilities is primarily due to a $0.18 million cash inflow from ~~accrued~~accounts payable, ~~expense~~partially ~~and~~offset ~~other~~by ~~current~~a ~~liabilities~~$0.1 ~~due~~million tocash ~~differences~~outflow infrom ~~the~~accrued ~~timing~~expenses ofand ~~disbursements~~other current liabilities and a $0.23 million cash outflow from ~~prepaid~~ prepaid expenses.

Cash Flows (Used) ~~Provided~~in by Investing Activities

Net cash used in investing activities for the ~~three~~six months ended ~~March~~June 3130, 2025, was $0.4 million,~~000,~~ resulting from $0.4 million in diagnostic asset purchases and purchases of property, plant and equipment ~~of $4,000~~.

~~There~~Net ~~was no~~ cash ~~flow~~used ~~from~~in investing activities for the ~~three~~six months ended ~~March~~June 3130, 2024, resulted from net purchases of short term investments of $0.2 million and purchases of PP&E during the year.

Cash Flows Provided by Financing Activities

Net cash provided by financing activities for the ~~three~~six months ended ~~March~~June 3130, 2025, was $5.9.7 million, resulting from proceeds from the issuance of common shares related to the ATM program of $811.19 million., ~~This~~partially ~~was~~ offset by repayments of notes payable of $0.62 million, repayments of notes payable – related parties of $0.4 million, repayment of convertible notes payable – related parties of $0.9 million ~~and~~ , repayment of convertible notes payable of $0.67 million, and treasury stock purchases of $0.1 million.

~~There~~Net ~~was no~~ cash ~~flow~~provided ~~from~~by financing activities for the ~~three~~six months ended ~~March~~June 3130, 2024, was $0.1 million, resulting from the proceeds on the issuance of the April 2024 warrants.

Contractual Obligations and Other Commitments

Laboratory Lease

We are the lessee under a laboratory space lease. The annual rent payments are $0.1 million for the years ending December 31, 2025 and December 31, 2026. The laboratory space lease has a remaining lease term of approximately two years.

Critical Accounting Estimates

The preparation of financial statements in conformity with U.S. GAAP requires us to make estimates, judgments and assumptions that affect the amounts reported in the Consolidated Financial Statements. These estimates, judgments and assumptions are evaluated on an ongoing basis. We base our estimates on historical experience and on various other assumptions that we believe are reasonable at that time, the results of which form the basis for making judgments about the carrying values of assets and liabilities that are not readily apparent from other sources. Actual results may differ materially from those estimates. The accounting policies that reflect our more significant estimates, judgments and assumptions and which we believe are the most critical to aid in fully understanding and evaluating our reported financial results include the following:

Fair Value of Convertible Notes

The Company has elected the fair value measurement option for convertible debt with embedded derivatives that would otherwise require bifurcation, and has recorded the entire hybrid financial instrument at fair value under the guidance in ASC Topic 825, Financial Instruments. To value the convertible debt, the Company utilizes Binomial Lattice Pricing Models. The Binomial Lattice Pricing Models involve the ~~construction~~ construction of various intermediate lattices: stock price tree, conversion value tree, conversion probability tree, and discount rate tree. In doing so, we assume the holders act rationally to maximize return and minimize cost at each decision point. We computed the notes payoff at maturity and at intermediate decision nodes based upon the better of (i) conversion or (ii) repayment of principal and interest.

The significant inputs and assumptions used to estimate the fair value include: (i) the Company’s stock price; (ii) the term of the convertible debt; (iii) the sum of the notes’ principal and unpaid accrued interest; (iv) expected volatility; (v) risk-free interest rate; (vi) the corporate bond yield; (vii) the credit spread; (viii) probability of default; and (ix) the estimated recovery upon default. Any change to the unobservable inputs to estimate fair value could produce significantly higher or lower fair value measurements and result in a material change within the financial statements.

The convertible debt will subsequently be remeasured at fair value each reporting date until settled or converted.

Fair Value of Warrants

The Company has issued warrants to investors in our debt and equity offerings. The Company has also issued warrants to service providers in relation to our financing offerings. We evaluate all warrants issued to determine the appropriate classification under ASC 480 and ASC 815.

For warrants that are determined to be equity-classified, we estimate the fair value at issuance and record the amounts to additional paid in capital. For warrants that are determined to be liability-classified, we estimate the fair value at issuance and each subsequent reporting date.

For the Company’s liability classified warrants, we estimate fair value using the Black-Scholes model. The significant inputs and assumptions used to estimate the fair value include: (i) the Company’s stock price; (ii) the risk-free rate; (iii) the expected volatility; and (iv) the dividend yield. The use of these valuation models requires the input of highly subjective assumptions. Any change to these inputs could produce significantly higher or lower fair value measurements and result in a material change within the financial statements.

Contingencies

In the ordinary course of business, we are involved in various legal proceedings that are complex in nature and have outcomes that are difficult to predict. We describe our legal proceedings and other matters that are significant or that we believe could become significant in Note 1514 to the consolidated financial statements. We record accruals for loss contingencies to the extent that we conclude it is probable that a liability has been incurred and the amount of the related loss can be reasonably estimated. We evaluate, on a quarterly basis, developments in legal proceedings and other matters that could cause an increase or decrease in the amount of the liability that has been accrued previously or modifications to contingency disclosures that are considered material.

Emerging Growth Company Status and Smaller Reporting Company Status

The Company is an emerging growth company, as defined in the Jumpstart Our Business Startups Act of 2012 (the “JOBS Act”). Under the JOBS Act, emerging growth companies can delay adopting new or revised accounting standards issued subsequent to the enactment of the JOBS Act until such time as those standards apply to private companies. The Company has elected to use this extended transition period for complying with new or revised accounting standards that have different effective dates for public and private companies until the earlier of the date that: (i) is no longer an emerging growth company or (ii) affirmatively and irrevocably opts out of the extended transition period provided in the JOBS Act. As a result, these financial statements may not be comparable to companies that comply with the new or revised accounting pronouncements as of public company effective dates.

Upon closing of the Merger, the surviving company remained an emerging growth company, as defined by the ~~Jumpstart~~JOBS ~~Our~~Act ~~Business Startups act of 2012,~~ until the earliest of (i) the last day of the combined entity’s first fiscal year following the fifth anniversary of the completion of MURF’s initial public offering;, (ii) the last day of the fiscal year in which the combined entity has total annual gross revenue of at least $1.235 billion;, (iii) the last day of the fiscal year in which the combined entity is deemed to be a large accelerated filer, which means the market value of the combined entity’s ~~common stock~~Common Stock that is held by non-affiliates exceeds $700.0 million as of the prior December 31st or (iv) the date on which the combined entity has issued more than $1.0 billion in non-convertible debt securities during the prior three year period.

3640

In addition, ~~Conduit~~CDT is a smaller reporting company as defined in the Securities Exchange Act of 1934 (as amended, the “Exchange Act”). The Company may continue to be a smaller reporting company even after we are no longer an emerging growth company. We may take advantage of certain of the scaled disclosures available to smaller reporting companies and will be able to take advantage of these scaled disclosures for so long as (i) ~~Conduit~~ CDT’s voting and non-voting ~~common~~ ~~stock~~Common Stock held by non-affiliates is less than $250.0 million measured on the last business day of our second fiscal quarter or (ii) ~~Conduit~~ CDT’s annual revenue is less than $100.0 million during the most recently completed fiscal year and its voting and non-voting ~~common~~ ~~stock~~Common Stock held by non-affiliates is less than $700.0 million measured on the last business day of its second fiscal quarter.

Item 3. Quantitative and Qualitative Disclosures About Market Risk.

As a smaller reporting company, we are not required to provide disclosure regarding quantitative and qualitative market risk.

Item 4. Controls and Procedures.

Evaluation of Disclosure Controls and Procedures

Disclosure controls and procedures are designed to ensure that information required to be disclosed by us in our Exchange Act reports is recorded, processed, summarized, and reported within the time periods specified in the SEC’s rules and forms, and that such information is accumulated and communicated to our management, including our principal executive officer and principal financial officer or persons performing similar functions, as appropriate to allow timely decisions regarding required disclosure.

Under the supervision and with the participation of our principal executive officer and principal financial officer, we conducted an ~~evaluation~~ evaluation of the effectiveness of our disclosure controls and procedures as of the end of the fiscal quarter ended ~~March~~June 3130, 2025 and for the comparison fiscal quarter ended ~~March~~June 3130, 2024, as such term is defined in Rules 13a-15(e) and 15d-15(e) under the Exchange Act. Based on this evaluation, our principal executive officer and principal financial officer concluded that during the periods covered by this Quarterly Report, our disclosure controls and procedures were not effective, due to material weaknesses previously identified and included in the Company’s most recent Form 10-K as not yet remediated as of the end of both such periods.

Changes in Internal Control over Financial Reporting

There have been no changes to in our internal control over financial reporting (as such term is defined in Rules 13a-15(f) and 15d-15(f) of the Exchange Act) during the most recent fiscal quarter.

37On April 12, 2025, Dr. David Tapolczay’s resignation as Chief Executive Officer of the Company became effective. Dr. Tapolczay’s resignation was not due to any disagreement with management or the Company’s operations, policies or practices. Effective April 15, 2025, the Board appointed Dr. Andrew Regan, as Chief Executive Officer.

PART II - OTHER INFORMATION

Item 1. Legal Proceedings.

~~Other~~The ~~than~~Company asis ~~set~~subject ~~forth~~to ~~below,~~certain claims and contingent liabilities that arise in the normal course of business. While we ~~are~~do not ~~currently~~expect ~~party~~that the toultimate orresolution ~~aware~~of any of ~~being~~these ~~subject~~pending toactions ~~any~~will have a material ~~legal~~effect ~~proceedings.~~on ~~However,~~our weconsolidated ~~may~~results ~~from~~of operations, financial ~~time~~position toor ~~time~~cash ~~become~~flows, alitigation ~~party~~is subject to ~~various~~inherent ~~legal~~uncertainties. ~~proceedings~~As ~~arising~~such, inthere ~~the~~can ~~ordinary~~be ~~course~~no ofassurance ~~our~~that ~~business,~~any ~~which~~pending ~~could~~legal ~~have~~action, does anot become material ~~adverse~~ ~~effect~~in onthe ~~our~~future. ~~business,~~As ~~financial~~of ~~condition~~June 30, or2025, ~~results~~a contingency of ~~operations~~$0.4 ~~Regardless~~million ofis ~~outcome,~~considered ~~litigation~~probable ~~could~~and ~~impact~~reasonably ~~our business~~estimable ~~due~~in relation to ~~defense~~the ~~and~~Company’s ~~settlement~~legal ~~costs~~proceedings. As such, ~~diversion~~the ofCompany ~~management~~accrued ~~resources~~an ~~and~~estimated ~~other~~liability ~~factors~~in the accompanying financial statements.

In August 2023, prior to the Business Combination, our now wholly-owned subsidiary, Conduit Pharmaceuticals Limited, received a letter from Strand Hanson Limited (“Strand”) claiming it was owed advisory fees pursuant to a previously executed letter. ~~Conduit~~CDT rejected the claim from Strand and disputed the substance of the letter in full. Following such rejection, on September 7, 2023, Strand filed a claim in the Business and Property Courts of England and Wales claiming it is entitled to be paid the sum of $2 million and, as a result of the completion of the Business Combination, to be issued 654,~~000~~333 shares ~~of common stock. As of March 31, 2025, the potential contingency~~ ~~is considered probable and reasonably estimable and as such, the Company accrued an estimated liability~~ of ~~$0.4~~Common ~~million in the accompanying financial statements~~Stock. The trial in this matter remains scheduled for October 20, 2025. We intend to vigorously defend against these claims. Regardless of its outcome, the litigation may impact our business due to, among other things, legal costs and the diversion of the attention of our management.

In November and December 2024, the Company received a letter from St George Street Capital and formal complaints filed with the Intellectual Property Office claiming the Company was assigned the US Application, and was not the sole owner, of the AZD 1656 co-crystal patent. In January 2025, ~~Conduit~~CDT issued a counter statement to the Intellectual Property Office disputing the claim filed by St George Street Capital. As of ~~March~~June 3130, 2025, the ~~damages~~range ~~sought~~of bypossible Stloss ~~George~~cannot ~~Street~~be ~~Capital~~estimated ~~are unknown~~ and ~~the potential contingency~~ is not considered probable. As such, the Company has not accrued a loss contingency in the accompanying financial statements. We intend to vigorously defend against these claims. Regardless of its outcome, the litigation may impact our business due to, among other things, legal costs and the diversion of the attention of our management.

Item 1A. Risk Factors.

As a smaller reporting company, we are not required to provide ~~information required~~disclosure byregarding ~~this~~material ~~item~~changes to our previously disclosed risk factors.

Item 2. Unregistered Sales of Equity Securities and Use of Proceeds.

No unregistered sales of equity securities occurred during the quarter ended ~~March~~June 3130, 2025 that were not previously reported.

OnThe ~~April~~following ~~10,~~table ~~2025,~~sets ~~the~~forth ~~Company’s~~repurchases ~~Board~~ of ~~Directors~~our ~~authorized~~Common aStock ~~share~~during ~~repurchase program under which~~ the ~~Company~~three ~~may~~months ~~purchase~~ended ~~up to~~June ~~$1.0 million of its outstanding common stock. As of March 31~~30, 2025~~, the Company has not repurchased any of its outstanding common stock.~~:1

(amounts in millions, except share and per share data)

Total number of shares purchased⁽¹⁾

Average price paid per share

Total number of shares purchased as part of the publicly announced program

Approximate dollar value of shares that may yet to be purchased under program

April 1, 2025 – April 30, 2025

[●]

May 1, 2025 – May 31, 2025

[●]

June 1, 2025 – June 30, 2025

[●]

Total

11,713

8.85

11,713

0.90

(1)

On April 10, 2025, the Board authorized a share repurchase program under which the Company may purchase up to $1.0 million of its outstanding Common Stock. The share repurchase program does not have an expiration date and may be adjusted or terminated by the Company at any time. There were 11,713 shares of Common Stock repurchased as part of the publicly announced share repurchase program during the three months ended June 30, 2025.

Item 3. Defaults Upon Senior Securities.

None.

Item 4. Mine Safety Disclosures.

Not applicable.

Item 5. Other Information.

During the ~~fiscal~~three ~~quarter~~month period ended ~~March~~June 3130, 2025, none of ~~the~~our ~~Company’s~~executive ~~directors~~officers or ~~officers~~directors (as defined in ~~Rule~~ ~~16a-1(f)~~Section 16 of the ~~Exchange~~Securities Exchange Act) ~~adopted~~of or1934, ~~terminated~~as ~~any~~amended), ~~contract~~adopted, ~~instruction~~terminated, or ~~written~~modified ~~plan~~a ~~for~~“Rule ~~the~~10-b5-1 ~~purchase~~trading arrangement” or ~~sale~~a of“non-Rule ~~Company~~10b5-1 ~~securities~~trading ~~that~~arrangement” ~~was~~(as ~~intended~~defined toin ~~satisfy~~Item ~~the affirmative defense conditions of Rule 10b5-1~~408(c) orof ~~any~~Regulation ~~“non~~S-~~Rule 10b5-1 trading arrangement~~K).

381 NOTE: Share repurchases made during each month to be provided by CDT.

Item 6. Exhibits

The following exhibits are filed as part of, or incorporated by reference into, this Quarterly Report on Form 10-Q.

EXHIBIT ~~INDEX2~~INDEX

Exhibit		Description
3.1		Certificate of Amendment filed with the Delaware Secretary of State on May 15, 2025 (incorporated by reference to the Company’s Current Report on Form 8-K filed on May 16, 2025).
3.2		Certificate of Amendment filed with the Delaware Secretary of State on August 5, 2025 (incorporated by reference to the Company’s Current Report on Form 8-K filed on August 8, 2025).
3.3		Second Amended and Restated Bylaws of the Company (incorporated by reference to the Company’s Current Report on Form 8-K filed on August 8, 2025).
10.1		Consulting Agreement, dated June 27, 2025, by and between the Company and Harold Eytan (incorporated by reference to the Company’s Registration Statement on Form S-3 filed on July 31, 2025).
10.2		Joint Development Agreement, dated June 3, 2025, by and between the Company and Manoira Corporation (incorporated by reference to the Company’s Current Report on Form 8-K filed on June 9, 2025).
10.3		CDT Equity Inc. Amended and Restated 2023 Stock Incentive Plan (incorporated by reference to the Company’s Current Report on Form 8-K filed on August 8, 2025).
31.1*		Certification of Principal Executive Officer pursuant to Securities Exchange Act Rules 13a-14(a) and 15(d)-14(a), as adopted pursuant to Section 302 of the Sarbanes-Oxley Act of 2002.
31.2*		Certification of Principal Financial Officer pursuant to Securities Exchange Act Rules 13a-14(a) and 15(d)-14(a), as adopted pursuant to Section 302 of the Sarbanes-Oxley Act of 2002.
32.1§		Certification of Principal Executive Officer pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002.
32.2§		Certification of Principal Financial Officer pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002.
101.INS*		Inline XBRL Instance Document.
101.CAL*		Inline XBRL Taxonomy Extension Calculation Linkbase Document.
101.SCH*		Inline XBRL Taxonomy Extension Schema Document.
101.DEF*		Inline XBRL Taxonomy Extension Definition Linkbase Document.
101.LAB*		Inline XBRL Taxonomy Extension Labels Linkbase Document.
101.PRE*		Inline XBRL Taxonomy Extension Presentation Linkbase Document.
104		Cover Page Interactive Data File (embedded within the Inline XBRL document).

Filed herewith.

In accordance with Item 601(b)(32)(ii) of Regulation S-K and SEC Release Nos. 33-8238 and 34-47986, Final Rule: Management’s Reports on Internal Control Over Financial Reporting and Certification of Disclosure in Exchange Act Periodic Reports, the certifications furnished in Exhibits 32.1 and 32.2 hereto is deemed to accompany this Quarterly Report on Form 10-Q and will not be deemed “filed” for purposes of Section 18 of the Exchange Act. Such certification will not be deemed to be incorporated by reference into any filing under the Securities Act or the Exchange Act, except to the extent that the registrant specifically incorporates it by reference.

3943

SIGNATURES

In accordance with the requirements of the Exchange Act, the registrant caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.

	CONDUIT PHARMACEUTICALS INC
	CDT EQUITY INC
May 14, 2025	By:	/s/ Dr. Andrew Regan
August 14, 2025	By:	/s/ Dr. Andrew Regan
	Name:	Dr. Andrew Regan
	Title:	Chief Executive Officer
		(Principal Executive Officer)
May 14, 2025	By:	/s/ James Bligh
August 14, 2025	By:	/s/ James Bligh
	Name:	James Bligh
	Title:	~~Interim~~ Chief Financial Officer
		(Principal Financial and Accounting Officer)

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