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 ~~September~~March 3031, ~~2025~~2026

☐	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: 001-36199

PULMATRIX, INC.

(Exact name of registrant as specified in its charter)

Delaware		46-1821392
(State or other jurisdiction of incorporation or organization)		(I.R.S. Employer Identification No.)
945 Concord Street, Suite 1217 Framingham, MA		01701
(Address of principal executive offices)		(Zip Code)

945 Concord Street, Suite 1217 Framingham, MA		01701
(Address of principal executive offices)		(Zip Code)

(888) 355-4440

Registrant’s telephone number, including area code

N/A

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

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 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. (Check one):

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 ☒

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

Title of each Class		Trading Symbol(s)		Name of each exchange on which registered
Common Stock, par value $0.0001 per share		PULM		The Nasdaq Stock Market LLC

As of ~~October~~May 1311, ~~2025~~2026, the registrant had 3,652,285 shares of common stock outstanding.

PULMATRIX, INC.

FORM 10-Q

FOR THE QUARTERLY PERIOD ENDED ~~SEPTEMBER~~MARCH 3031, ~~2025~~2026

TABLE OF CONTENTS

		Page No.
PART I—FINANCIAL INFORMATION
Item 1.	Condensed Consolidated Financial Statements (unaudited)	1
	Consolidated Balance Sheets as of September 30, 2025, and December 31, 2024	1
	Consolidated Balance Sheets as of March 31, 2026 and December 31, 2025	1
	Consolidated Statements of Operations for the Three and Nine Months Ended September 30, 2025, and 2024	2
	Consolidated Statements of Operations for the Three Months Ended March 31, 2026 and 2025	2
	Consolidated Statements of Stockholders’ Equity for the Three and Nine Months Ended September 30, 2025, and 2024	3
	Consolidated Statements of Stockholders’ Equity for the Three Months Ended March 31, 2026 and 2025	3
	Consolidated Statements of Cash Flows for the Nine Months Ended September 30, 2025, and 2024	4
	Consolidated Statements of Cash Flows for the Three Months Ended March 31, 2026 and 2025	4
	Notes to Condensed Consolidated Financial Statements	5
Item 2.	Management’s Discussion and Analysis of Financial Condition and Results of Operations	12
Item 3.	Quantitative and Qualitative Disclosures About Market Risk	23
Item 4.	Controls and Procedures	23
PART II—OTHER INFORMATION
Item 1.	Legal Proceedings	24
Item 1A.	Risk Factors	24
Item 2.	Unregistered Sales of Equity Securities and Use of Proceeds	2425
Item 3.	Defaults Upon Senior Securities	2425
Item 4.	Mine Safety Disclosures	2425
Item 5.	Other Information	2425
Item 6.	Exhibits	2425
SIGNATURES		2526

PART I—FINANCIAL INFORMATION

Item 1. Condensed Consolidated Financial Statements.

PULMATRIX, INC.

Consolidated Balance Sheets

(in thousands, except share and per share data)

	September 30, 2025			December 31, 2024
	March 31, 2026			December 31, 2025
	(unaudited)
Assets
Current assets:
Cash and cash equivalents	$	43,~~794~~324		$	94,~~521~~088
Prepaid expenses and other current assets		178			399
Restricted cash		700			-
Total current assets		4,972			9,920
Prepaid expenses and other current assets		465			41
Long-term restricted cash		10			10
Total current assets		4,489			4,129
Other long-term assets		-			13
Long-term restricted cash		7			10
Total assets	$	4,~~982~~496		$	94,~~943~~139
Liabilities and stockholders’ equity
Current liabilities:
Accounts payable	$	69651		$	~~809~~272
Accrued expenses and other current liabilities		~~180~~254			~~120~~57
Total current liabilities		~~249~~905			~~929~~329
Warrant liability		-			67
Total liabilities		905			329
Total liabilities		249			996
Commitments and contingencies (Note 9)		-			-
Commitments and contingencies (Note 8)		-
Stockholders’ equity:
Preferred Stock, $0.0001 par value — 500,000 shares authorized; 6,746 shares designated Series A convertible preferred stock; no shares issued and outstanding at September 30, 2025, and December 31, 2024		-			-
Preferred stock, $0.0001 par value — 500,000 shares authorized; 1,100 shares designated as Series B Convertible Preferred Stock; no shares issued and outstanding at March 31, 2026, and December 31, 2025; 1,000 shares of Series B Convertible Preferred Stock issuable at March 31, 2026		950			-
Common stock, $0.0001 par value — 200,000,000 shares authorized; 3,652,285 shares issued and outstanding at September 30, 2025, and December 31, 2024		-			-
Common stock, $0.0001 par value — 200,000,000 shares authorized; 3,652,285 shares issued and outstanding at March 31, 2026, and December 31, 2025		-			-
Additional paid-in capital		306,~~123~~131			306,~~103~~128
Accumulated deficit		(~~301~~303,~~390~~490	)		(~~297~~302,~~156~~318	)
Total stockholders’ equity		43,~~733~~591			83,~~947~~810
Total liabilities and stockholders’ equity	$	4,~~982~~496		$	94,~~943~~139

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

PULMATRIX, INC.

Consolidated Statements of Operations

(in thousands, except share and per share data)

(unaudited)

	2025			2024			2025			2024
	2026			2025
	Three Months Ended September 30,						Nine Months Ended September 30,
	Three Months Ended March 31,
	2025			2024			2025			2024
	2026			2025
Revenues	$	-		$	366		$	-		$	7,803
Operating expenses:
Operating expenses:
Research and development	$	3		$	19
Research and development		8			814			41			7,160
General and administrative		1,289			1,828
General and administrative		858			2,209			4,220			5,836
Total operating expenses		1,292			1,847
Loss on MannKind Transaction		-			-			-			2,618
Loss from operations		(1,292	)		(1,847	)
Total operating expenses		866			3,023			4,261			15,614
Other income (expense):
Loss from operations		(866	)		(2,657	)		(4,261	)		(7,811	)
Interest income		12			53
Other income (expense):
Fair value adjustment of warrants		-			66
Interest income		30			101			124			394
Other income (expense), net		108			(80	)
Fair value adjustment of warrants		-			-			67			-
Total other income (expense), net		120			39
Other expense, net		(41	)		(31	)		(164	)		(156	)
Net loss	$	(1,172	)	$	(1,808	)
Total other income (expense), net		(11	)		70			27			238
Net loss per share attributable to common stockholders – basic and diluted	$	(0.32	)	$	(0.50	)
Net loss	$	(877	)	$	(2,587	)	$	(4,234	)	$	(7,573	)
Weighted average common shares outstanding – basic and diluted		3,652,285			3,652,285
Net loss per share attributable to common stockholders – basic and diluted	$	(0.24	)	$	(0.71	)	$	(1.16	)	$	(2.07	)
Weighted average common shares outstanding – basic and diluted		3,652,285			3,652,285			3,652,285			3,652,285

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

PULMATRIX, INC.

Consolidated Statements of Stockholders’ Equity

(in thousands, except share data)

(unaudited)

	Shares		Amount		~~Capital~~Shares		~~Deficit~~Amount			~~Equity~~Capital			Deficit			Equity
	Common Stock				Additional Paid-in		Accumulated			Total Stockholders’
	Series B Convertible Preferred Stock				Common Stock					Additional Paid-in			Accumulated			Total Stockholders’
	Shares		Amount		~~Capital~~Shares		~~Deficit~~Amount			~~Equity~~Capital			Deficit			Equity
Balance — January 1, 2025		3,652,285	$	-	$	306,103	$	(297,156	)	$	8,947
Balance — January 1, 2026		-	$	-		3,652,285	$	-		$	306,128		$	(302,318	)	$	3,810
Stock-based compensation		-		-		8		-			8
Proceeds received, net of issuance costs, for Series B Convertible Preferred Stock prior to issuance		-		950		-		-			-			-			950
Net loss		-		-		-		(1,808	)		(1,808	)
Stock-based compensation		-		-		-		-			3			-			3
Balance — March 31, 2025		3,652,285	$	-	$	306,111	$	(298,964	)	$	7,147
Net loss		-		-		-		-			-			(1,172	)		(1,172	)
Stock-based compensation		-		-		6		-			6
Balance — March 31, 2026		-	$	950		3,652,285	$	-		$	306,131		$	(303,490	)	$	3,591
Net loss		-		-		-		(1,549	)		(1,549	)
Balance — June 30, 2025		3,652,285	$	-	$	306,117	$	(300,513	)	$	5,604
Stock-based compensation		-		-		6		-		$	6
Net loss		-		-		-		(877	)		(877	)
Balance — September 30, 2025		3,652,285	$	-	$	306,123	$	(301,390	)	$	4,733

	Common Stock				Additional Paid-in		Accumulated			Total Stockholders’
	Series B Convertible Preferred Stock				Common Stock					Additional Paid-in			Accumulated			Total Stockholders’
	Shares		Amount		~~Capital~~Shares		~~Deficit~~Amount			~~Equity~~Capital			Deficit			Equity
Balance — January 1, 2024		3,652,285	$	-	$	305,592	$	(287,597	)	$	17,995
Balance — January 1, 2025		-	$	-		3,652,285	$	-		$	306,103		$	(297,156	)	$	8,947
Stock-based compensation		-		-		198		-			198
Balance		-	$	-		3,652,285	$	-		$	306,103		$	(297,156	)	$	8,947
Net income		-		-		-		825			825
Stock-based compensation		-		-		-		-			8			-			8
Balance — March 31, 2024		3,652,285	$	-	$	305,790	$	(286,772	)	$	19,018
Net loss		-		-		-		-			-			(1,808	)		(1,808	)
Stock-based compensation		-		-		103		-			103
Balance — March 31, 2025		-	$	-		3,652,285	$	-		$	306,111		$	(298,964	)	$	7,147
Net loss		-		-		-		(5,811	)		(5,811	)
Balance		-	$	-		3,652,285	$	-		$	306,111		$	(298,964	)	$	7,147
Balance — June 30, 2024		3,652,285	$	-	$	305,893	$	(292,583	)	$	13,310
Balance		3,652,285	$	-	$	305,893	$	(292,583	)	$	13,310
Stock-based compensation		-		-		197		-		$	197
Net loss		-		-		-		(2,587	)		(2,587	)
Net income (loss)		-		-		-		(2,587	)		(2,587	)
Balance — September 30, 2024		3,652,285	$	-	$	306,090	$	(295,170	)	$	10,920
Balance		3,652,285	$	-	$	306,090	$	(295,170	)	$	10,920

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

PULMATRIX, INC.

Consolidated Statements of Cash Flows

(in thousands)

(unaudited)

	2025			2024
	2026			2025
	Nine Months Ended September 30,
	Three Months Ended March 31,
	2025			2024
	2026			2025
Cash flows from operating activities:
Net loss	$	(41,~~234~~172	)	$	(71,~~573~~808	)
Adjustments to reconcile net loss to net cash used in operating activities:
Depreciation and amortization		-			106
Stock-based compensation		3			8
Amortization of operating lease right-of-use asset		-			329
Fair value adjustment of warrants		-			(66	)
Stock-based compensation		20			498
Fair value adjustment of warrants		(67	)		-
Loss on MannKind Transaction		-			2,618
Changes in operating assets and liabilities:
Accounts receivable		-			~~905~~(16	)
Prepaid expenses and other current assets		~~221~~(424	)		~~101~~82
Other long-term assets		13-			~~122~~13
Accounts payable		~~(740~~379	)		(~~1,542~~152	)
Accrued expenses and other current liabilities		60147			~~(341~~126	)
Operating lease liability		-			(333	)
Net cash used in operating activities		(1,067	)		(1,813	)
Deferred revenue		-			(4,345	)
Cash flows from financing activities:
Net cash used in operating activities		(4,727	)		(9,455	)
Proceeds from sale of Series B Convertible Preferred Stock		1,000			-
Cash flows from investing activities:
Cash provided by financing activities		1,000			-
Purchases of property and equipment		-			(398	)
Net decrease in cash, cash equivalents and restricted cash		(67	)		(1,813	)
Net cash used in investing activities		-			(398	)
Cash, cash equivalents and restricted cash — beginning of period		4,098			9,531
Net decrease in cash, cash equivalents and restricted cash		(4,727	)		(9,853	)
Cash, cash equivalents and restricted cash — end of period	$	4,031		$	7,718
Cash, cash equivalents and restricted cash — beginning of period		9,531			20,645
Cash, cash equivalents and restricted cash — end of period	$	4,804		$	10,792
Reconciliation of cash, cash equivalents and restricted cash to the consolidated balance sheets:
Cash and cash equivalents	$	43,~~794~~324		$	107,~~782~~708
Long-term restricted cash		10			10
Restricted cash		700			-
Total cash, cash equivalents and restricted cash	$	4,804		$	10,792
Long-term restricted cash		7			10
Supplemental disclosures of non-cash investing and financing information:
Total cash, cash equivalents and restricted cash	$	4,031		$	7,718
Reduction of operating lease right-of-use asset and lease liability upon lease modification	$	-		$	8,423
Cash, cash equivalents and restricted cash — end of period	$	4,031		$	7,718
Supplemental disclosures of non-cash financing information:
Preferred stock issuance costs not yet paid	$	50		$	-

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

PULMATRIX, INC.

Notes to Condensed Consolidated Financial Statements (Unaudited)

(in thousands, except share and per share data)

1. Organization

Pulmatrix, Inc. (“Pulmatrix” or the “Company”) was incorporated in 2013 as a Delaware corporation. The Company is a biopharmaceutical company that has focused on the development of a novel inhaled therapeutic products intended to prevent and treat migraine and respiratory diseases with important unmet medical needs using its patented iSPERSE™ technology. The Company’s proprietary dry powder delivery platform, iSPERSE™, is engineered to deliver small, dense particles with highly efficient dispersibility and delivery to the airways, which can be used with an array of dry powder inhaler technologies and can be formulated with a variety of drug substances.

Agreement and Plan of Merger and Reorganization

On ~~November~~March 1326, ~~2024~~2026, Pulmatrix and ~~Cullgen~~Eos SENOLYTIX, Inc., a Delaware corporation (“~~Cullgen~~Eos”), entered into an Agreement and Plan of ~~Merger~~ Merger and Reorganization, ~~as amended by Amendment No. 1 thereto on April 7, 2025~~ (the “Merger Agreement”), pursuant to which, among other matters, ~~PCL~~PUOS Merger Sub, Inc., a direct wholly owned subsidiary of Pulmatrix (“Merger Sub”), will merge with and into ~~Cullgen~~ Eos, with ~~Cullgen~~Eos ~~surviving~~continuing as the surviving corporation and a wholly owned subsidiary of Pulmatrix (the “Merger”). In connection with the Merger, Eos and ~~the~~Pulmatrix ~~surviving~~entered ~~corporation~~into definitive agreements for concurrent private financings of ~~the~~$19 ~~merger~~million in aggregate gross proceeds (collectively, the “~~Merger~~Financings”), including a $1.0 million investment in Pulmatrix.

~~Pursuant~~Under tothe Exchange Ratio formula set forth in the Merger Agreement, ~~prior~~upon to the closing of the Merger (the “Closing”), ~~Pulmatrix~~on ~~currently~~a ~~expects~~pro toforma basis ~~declare~~and abased ~~cash dividend~~upon the number of shares of Pulmatrix common stock expected to be issued in the Merger, pre-Merger ~~Pulmatrix~~Eos stockholders, including ~~equal~~investors participating in the ~~aggregate~~Financings toand ~~Pulmatrix’s~~holders ~~reasonable,~~of ~~good~~shares ~~faith~~issued ~~approximation~~in payment of placement agent and advisory fees, will own approximately 94% of the ~~amount~~combined bycompany ~~which~~and Pulmatrix’s ~~net~~stockholders ~~cash~~will ~~(as~~own ~~determined~~approximately ~~pursuant~~6% toof the ~~Merger~~combined ~~Agreement)~~company ~~will~~on ~~exceed~~a ~~$2.5~~fully-diluted basis ~~million,~~(excluding ~~subject~~any ~~to certain~~shares ~~adjustments~~reserved ~~and~~for ~~limitations~~future ~~(such~~grants ~~excess~~under ~~amount,~~Pulmatrix’s ~~the~~equity ~~“Cash~~incentive ~~Dividend”~~plans).

~~Subject~~The toconsummation ~~the terms and conditions~~ of the Merger ~~Agreement,~~is atsubject ~~the~~to ~~Closing,~~approval ~~(a)~~by ~~each~~Pulmatrix ~~then-outstanding~~stockholders ~~share~~and ofEos ~~Cullgen~~stockholders, ~~common~~as ~~stock~~well as other ~~than dissenting~~customary ~~shares~~closing conditions, ~~will~~including ~~be converted into~~ the ~~right~~effectiveness toof ~~receive~~ a ~~number~~registration ofstatement ~~shares~~filed ~~of Pulmatrix common stock calculated in accordance~~ with the ~~Merger~~Securities ~~Agreement~~and ~~(the “~~Exchange ~~Ratio”),~~Commission ~~(b)~~in ~~each~~connection ~~then-outstanding share of Cullgen preferred stock, other than~~with ~~dissenting~~the ~~shares,~~transaction ~~will~~and beNasdaq’s ~~converted~~approval ~~into~~of the ~~right~~listing ~~to receive a number~~ of the shares of Pulmatrix common stock ~~equal~~ to ~~the~~be ~~number~~issued ofin ~~shares of~~connection ~~Cullgen~~with ~~common stock issuable upon conversion of each share of Cullgen preferred stock multiplied by~~ the ~~Exchange Ratio and (c) each~~ ~~then-outstanding~~Merger. ~~option~~If tothe ~~purchase~~Merger ~~Cullgen~~is ~~common stock~~completed, ~~whether~~the ~~vested~~business orof ~~unvested,~~Eos will becontinue ~~assumed~~as ~~by Pulmatrix, subject to adjustment to reflect~~ the ~~Exchange~~business ~~Ratio~~of ~~as set forth in~~ the ~~Merger~~combined ~~Agreement~~company.

InThe ~~connection~~Merger ~~with~~Agreement ~~the~~contains ~~Merger:~~certain ~~(i)~~termination ~~each~~rights ~~share~~of each of Pulmatrix ~~common stock that is issued~~ and ~~outstanding~~Eos. atAt the Effective Time ~~(as defined below) of the Merger will remain issued and outstanding and such shares~~, ~~subject to~~ the ~~proposed~~board ~~Pulmatrix~~of ~~reverse~~directors ~~stock split, will be unaffected by the Merger; (ii) each option to acquire shares~~ of Pulmatrix ~~common stock outstanding but then not vested or exercisable~~ ~~shall~~is beexpected ~~accelerated in full; (iii) each option~~ to ~~acquire~~consist ~~shares~~ of ~~Pulmatrix~~six ~~common~~members, ~~stock~~one ~~with an exercise price per share greater than $10.00 per share shall be cancelled for no consideration; (iv) each option to acquire shares~~ of ~~Pulmatrix~~which ~~common stock with an exercise price less than or equal to the Pulmatrix Closing Price (as defined herein)~~ will be converted into the right to receive the number of shares underlying such Pulmatrix option, reduced as set forth in the Merger Agreement; (v) each option to acquire shares of Pulmatrix common stock with an exercise price greater than the volume weighted average closing trading price of a ~~share~~director ofdesignated ~~Parent Common Stock on Nasdaq for the five (5) consecutive trading days ending three (3) trading days immediately prior to the Closing Date as reported~~ by ~~Bloomberg~~ ~~L.P. (the “~~Pulmatrix ~~Closing Price”)~~, ~~but less than $10.00 per share, will remain outstanding;~~ and ~~(vi) each warrant to acquire shares of Pulmatrix common stock that is outstanding and unexercised immediately prior to~~ the ~~Effective~~remainder ~~Time~~ of ~~the Merger shall survive the Closing and remain outstanding in accordance with its terms; provided that the holders of any such warrants~~ which ~~remain outstanding~~will ~~following~~be ~~closing may elect to require Pulmatrix to pay such holders cash in exchange for the termination of the remaining~~designated ~~unexercised portion of such warrants if contemplated~~ by ~~the terms of such warrants~~Eos.

5The Company’s future operations are highly dependent on the success of the Merger and there can be no assurances that the Merger will be successfully consummated. If the Merger is not consummated, the Company’s board of directors may decide to pursue a dissolution and liquidation.

Under the Exchange Ratio formula in the Merger Agreement, upon the Closing, on a pro forma basis and based upon the number of shares of Pulmatrix common stock expected to be issued in the Merger, pre-Merger Cullgen stockholders will own approximately 96.4% of the combined company and pre-Merger Pulmatrix stockholders will own approximately 3.6% of the combined company on a fully-diluted basis (excluding out-of-the-money options and warrants and any shares reserved for future grants under Pulmatrix’s equity incentive plans). Under certain circumstances further described in the Merger Agreement, the ownership percentages may be adjusted upward or downward based on Pulmatrix’s net cash at the Closing.

The Exchange Ratio assumes (i) a valuation for Pulmatrix of $10.5 million (comprised of $8 million in enterprise value and $2.5 million in cash) and (ii) a valuation for Cullgen of $280.0 million. The Exchange Ratio is also based on the relative capitalization of each of Pulmatrix and Cullgen, for which, for the purposes of calculating the Exchange Ratio, the shares of Pulmatrix common stock underlying Pulmatrix’s in-the-money stock options outstanding immediately prior to the time of the Closing (the “Effective Time”), as adjusted to take into account the Cash Dividend will be deemed outstanding, and all shares of Cullgen common stock underlying outstanding Cullgen’s stock options will be deemed outstanding, subject to certain exceptions as set forth in the Merger Agreement.

On June 16, 2025, the Company held a special meeting in lieu of the annual meeting of Pulmatrix stockholders, at which the Company’s stockholders approved the Merger and related proposals. The Closing is subject to other customary closing conditions, including Nasdaq’s approval of the listing of the shares of Pulmatrix common stock to be issued in connection with the Merger and approval from the China Security Regulatory Commission (“CSRC”) pursuant to the Trial Administrative Measures of Overseas Securities Offering and Listing by Domestic Enterprises (the “Trial Measures”), No. 1 to No. 6 Supporting Guidance Rules, the Notice on Administration Arrangements for the Filing of Overseas Listings by Domestic Enterprises and the relevant CSRC Answers to Reporter Questions on the official website of the CSRC. These regulations established a filing-based regime to regulate overseas offerings and listings by Chinese domestic companies. As of the date of this filing, Pulmatrix has not yet received approval from the CSRC to complete the Merger. As previously disclosed, on August 1, 2025, Pulmatrix and Cullgen, as provided for in the Merger Agreement, mutually agreed to extend the “End Date”, a term defined in the Merger Agreement, by 60 days from August 13, 2025, to October 12, 2025. The Merger Agreement does not have a defined term and does not terminate on the “End Date”. The “End Date” is simply the date at which certain termination options become available to either party.

The Merger Agreement contains certain termination rights of each of Pulmatrix and Cullgen. Upon termination of the Merger Agreement under specified circumstances, Pulmatrix may be required to pay Cullgen a termination fee of $420,000, and in certain other circumstances, Cullgen may be required to pay Pulmatrix a termination fee of either $2,800,000 or $8,400,000.

If the Merger is completed, the business of Cullgen will continue as the business of the combined company. Concurrent with the Merger, the Company will seek to monetize its intellectual property, including iSPERSE™ and its clinical assets (the “Asset Sale”).

The Company’s future operations are highly dependent on the success of the Merger and there can be no assurances that the Merger will be successfully consummated. There can be no assurance that the strategic review process or any transaction relating to a specific asset, including the Merger and any Asset Sale, will result in the Company pursuing such a transaction, or that any transactions, if pursued, will be completed on terms favorable to Pulmatrix and its stockholders in the existing Pulmatrix entity or any possible entity that results from a combination of entities. If the strategic review process is unsuccessful, and if the Merger is not consummated, the Company’s board of directors may decide to pursue a dissolution and liquidation.

2. Summary of Significant Accounting Policies and Recent Accounting Standards

Basis of Presentation

The condensed consolidated financial statements of the Company included herein have been prepared pursuant to the rules and regulations of the Securities and Exchange Commission (the “SEC”). Certain information and footnote disclosures normally included in financial statements prepared in accordance with generally accepted accounting principles in the United States of America (“U.S. GAAP”) have been condensed or omitted from this report, as is permitted by such rules and regulations. Accordingly, these condensed consolidated financial statements should be read in conjunction with the consolidated financial statements and notes thereto included in the Company’s Annual Report on Form 10-K for the fiscal year ended December 31, ~~2024~~2025, filed with the SEC on ~~March~~February 2126, ~~2025~~2026 (the “Annual Report”).

The financial information as of ~~September~~March 3031, ~~2025~~2026, and for the three ~~and nine~~ months ended ~~September~~March 3031, ~~2025,~~2026 and ~~2024~~2025, is unaudited. In the opinion of management, all adjustments (including those which are normal and recurring) considered necessary for a fair presentation of the interim financial information have been included. The balance sheet data as of December 31, ~~2024~~2025, was derived from audited consolidated financial statements. The results of the Company’s operations for any interim periods are not necessarily indicative of the results that may be expected for any other interim period or for a full fiscal year.

~~The~~Liquidity ~~Company’s future operations are highly dependent on the success of the Merger~~ and ~~there~~going can be no assurances that the Merger will be successfully consummated. If the Merger is not consummated, the Company believes that its cash and cash equivalents as of September 30, 2025, would be adequate to fund its operating expenses for at least twelve months from the date these condensed consolidated financial statements are issued. However, in order to continue development of its programs, the Company would need to secure substantial additional funding in the future, from one or more equity or debt financings, collaborations, or other sources. Additional funding may not be available to the Company on acceptable terms, or at all. The Company’s board of directors may also decide to pursue a dissolution and liquidation in lieu of continuing program development.concern

The accompanying unaudited financial statements have been prepared assuming that the Company will continue as a going concern within one year after the date that the financial statements are issued. The Company’s future operations are highly dependent on the success of the Merger and there can be no assurances that the Merger will be successfully consummated. If the Merger is not consummated, the Company may seek other strategic alternatives or pursue a dissolution and liquidation.

The Company anticipates that its cash position is sufficient to fund its operations at least through the anticipated closing of the proposed Merger with Eos. However, the Company expects to incur significant costs in connection with the Merger and even if the Merger is ultimately not consummated, including legal and professional services costs related to filing registration statements with the SEC and obtaining shareholder approval.

As of March 31, 2026, the Company had $3.3 million in cash and cash equivalents, as well as $0.7 million in restricted cash that would become unrestricted following consummation of the Merger or upon any termination of the Merger Agreement in accordance with its terms. Management believes that, given the Company’s current cash position and forecasted negative cash flows from operating activities over the next twelve months, there is substantial doubt about its ability to continue as a going concern after the date that is one year from the date that these financial statements are issued without the closing of the Merger.

The accompanying financial statements do not include any adjustments that might be necessary if the Company is not able to continue as a going concern.

In order to continue development of its programs, the Company would need to secure substantial additional funding in the future, from one or more equity or debt financings, collaborations, or other sources. Additional funding may not be available to the Company on acceptable terms, or at all.

Should the Company continue development of its product candidates, the Company would be subject to risks and uncertainties. The ongoing research and development activities will be subject to extensive regulation by numerous governmental authorities in the United States. Prior to marketing in the United States, any drug developed by the Company must undergo rigorous preclinical and clinical testing and an extensive regulatory approval process implemented by the United States Food and Drug Administration (“FDA”) under the Food, Drug and Cosmetic Act. The Company has limited experience in conducting and managing the preclinical and clinical testing necessary to obtain regulatory approval. There can be no assurance that the Company will not encounter problems in the clinical trials that will cause the Company or the FDA to delay or suspend clinical trials.

The Company’s success in developing its product candidates would depend in part on its ability to obtain patents and product license rights, maintain trade secrets, and operate without infringing on the property rights of others, both in the United States and other countries. There can be no assurance that patents issued to or licensed by the Company will not be challenged, invalidated, circumvented, or that the rights granted thereunder will provide proprietary protection or competitive advantages to the Company.

Use of Estimates

In preparing the condensed consolidated financial statements in conformity with U.S. GAAP, management is required to make estimates and assumptions that affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities at the date of the condensed consolidated financial statements, as well as the reported amounts of expenses during the reporting period. Due to inherent uncertainty involved in making estimates, actual results may differ from these estimates. On an ongoing basis, the Company evaluates its estimates and assumptions, with any changes applied prospectively.

Concentrations of Credit Risk

Cash and cash equivalents is a financial instrument that potentially subjects the Company to concentrations of credit risk. For all periods presented, substantially all of the Company’s cash was deposited in accounts at a single financial institution that management believes is creditworthy, and the Company has not incurred any losses to date. The Company is exposed to credit risk in the event of default by this financial institution for amounts in excess of the Federal Deposit Insurance Corporation insured limits.

For the three and nine months ended September 30, 2025, the Company recognized no revenue. For the three and nine months ended September 30, 2024, revenue from two customers accounted for 100% of revenue recognized in the accompanying condensed consolidated financial statements.

Summary of Significant Accounting Policies

The Company’s significant accounting policies are described in Note 2, Summary of Significant Accounting Policies and Recent Accounting Standards, in the Annual Report. During the ~~nine~~three months ended ~~September~~March 3031, ~~2025~~2026, the Company did not make any changes to its significant accounting policies.

Recent Accounting Pronouncements

From time to time, new accounting pronouncements are issued by the Financial Accounting Standards Board (“FASB”) or other standard setting bodies that are adopted by the Company as of the specified effective date. The Company did not adopt any new accounting pronouncements during the ~~nine~~three months ended ~~September~~March 3031, ~~2025~~2026, that had a material effect on its condensed consolidated financial statements.

In ~~December~~November ~~2023~~2024, the FASB issued Accounting ~~Standard~~Standards Update (“ASU”) ~~2023~~2024-0903, Income ~~Taxes~~Statement—Reporting Comprehensive Income—Expense Disaggregation Disclosures (~~Topic~~Subtopic ~~740~~220-40): ~~Improvements~~Disaggregation toof Income ~~Tax~~ ~~Disclosures~~Statement Expenses (“ASU ~~2023~~2024-0903”). The guidance in ASU ~~2023~~2024-0903 ~~improves~~requires disclosure about the ~~transparency~~types of ~~income~~costs ~~tax~~and ~~disclosures~~expenses byincluded ~~greater disaggregation of information~~ in ~~the~~certain ~~rate~~expense ~~reconciliation~~captions ~~and~~presented on the income ~~taxes~~statement. ~~paid~~The ~~disaggregated~~new bydisclosure ~~jurisdiction.~~requirements ~~ASU~~are ~~2023-09 is~~ effective for the Company’s ~~for~~annual ~~the~~periods ~~annual~~beginning ~~period~~after ~~ending~~December 15, 2026, and interim periods beginning after December 3115, ~~2025~~2027, with early adoption permitted. The Company is currently evaluating the impact that ~~the~~ adoption ~~may have~~of onASU ~~its~~2024-03 ~~annual~~may ~~income~~have ~~tax~~on ~~disclosures in~~ its consolidated financial statements.

In ~~November~~April ~~2024~~2026, the FASB issued ASU ~~2024~~2026-0301, ~~Income~~Equity ~~Statement—Reporting Comprehensive Income—Expense Disaggregation Disclosures~~ (~~Subtopic~~Topic ~~220-40~~505): ~~Disaggregation~~Initial Measurement of ~~Income~~Paid-in-Kind ~~Statement~~Dividends ~~Expenses~~on Equity-Classified Preferred Stock (“ASU ~~2024~~2026-0301”). The guidance in ASU ~~2024~~2026-0301 ~~requires~~clarifies ~~disclosure about~~how ~~the~~issuers ~~types~~initially ofmeasure ~~costs~~paid-in-kind ~~and~~(“PIK”) dividends ~~expenses~~on ~~included~~equity-classified inpreferred ~~certain~~stock ~~expense~~by ~~captions~~requiring ~~presented~~issuers onto use the ~~income~~PIK ~~statement.~~dividend ~~The~~rate ~~new~~stated ~~disclosure~~in ~~requirements~~the preferred stock agreement. ~~are~~ASU 2026-01 will be effective for the Company’s annual reporting periods beginning after December 15, 2026, and for interim reporting periods ~~beginning~~within ~~after~~those ~~December 15,~~annual ~~2027~~periods, with early adoption permitted. Entities may apply the amendments on either a prospective basis or a modified retrospective basis for equity-classified preferred stock instruments that are outstanding as of the initial application date. The Company is currently evaluating the impact that adoption of ASU ~~2024~~2026-0301 may have on its consolidated financial statements.

As of ~~September~~March 3031, ~~2025~~2026, there are no other new, or existing recently issued, accounting pronouncements that are of significance, or potential significance, that impact the Company’s condensed consolidated financial statements.

3. Prepaid Expenses and Other Current Assets

Prepaid expenses and other current assets consisted of the following:

	September 30, 2025		December 31, 2024
	March 31, 2026		December 31, 2025
Insurance	$	~~112~~338	$	~~200~~3
Software and hosting costs		47		194
Other		62120		~~180~~34
Total prepaid expenses and other current assets	$	~~178~~465	$	~~399~~41

4. Accrued Expenses and Other Current Liabilities

Accrued expenses and other current liabilities consisted of the following:

	September 30, 2025		December 31, 2024
	March 31, 2026		December 31, 2025
Legal and patents	$	67230	$	112
Wages and incentives		3714		3841
Other		7610		7114
Total accrued expenses and other current liabilities	$	~~180~~254	$	~~120~~57

5. Preferred Stock

The Company’s amended and restated certificate of incorporation (the “Articles”) provides for a class of authorized stock known as preferred stock, consisting of 500,000 shares, $0.0001 par value per share, issuable from time to time in one or more series.

The Company previously designated 6,746 shares as Series A Convertible Preferred Stock, none of which remain issued and outstanding as of March 31, 2026 or December 31, 2025.

During the three months ended March 31, 2026, the Company designated 1,100 shares of Series B Convertible Preferred Stock, par value of $0.0001 and stated value equal to $1,000 (the “Series B Convertible Preferred Stock”).

In connection with the entry into the Merger Agreement, Pulmatrix entered into a Securities Purchase Agreement (the “Purchase Agreement”), dated as of March 26, 2026, with an affiliate of Eos (the “Buyer”), pursuant to which the Company agreed to issue and sell to the Buyer in a private placement an aggregate of 1,000 shares of Series B Convertible Preferred Stock for aggregate gross proceeds of $1.0 million, which the Company received during the three months ended March 31, 2026. The Company delivered the shares of Series B Convertible Preferred Stock to the Buyer on April 16, 2026.

The following paragraph summarizes the terms of the Series B Convertible Preferred Stock.

Conversion Price: The Series B Convertible Preferred Stock is convertible into the shares of Pulmatrix common stock at an initial conversion price of $2.20 per share (the “Conversion Price”). The Conversion Price is subject to customary adjustments for stock dividends, stock splits, reclassifications, stock combinations and the like (subject to certain exceptions). Each conversion of Series B Convertible Preferred Stock is subject to certain beneficial ownership limitations.

Optional conversion: Each share of Series B Convertible Preferred Stock is convertible at any time after the date that is 90 days following the initial date of issuance (the “Original Issuance Date”) at the election of the holder.

Automatic conversion: Effective as of 5:00 p.m. Eastern time on the fifth business day after the date that is the earlier of (i) the one-year anniversary from the Original Issuance Date (ii) the closing date of the Merger, each share of Series B Convertible Preferred Stock then outstanding shall automatically convert into shares of common stock.

Cumulative dividends: Holders of Series B Convertible Preferred Stock are entitled to receive cumulative dividends at eight percent (8.0%) per annum, payable on each conversion date (with respect only to Series B Convertible Preferred Stock being converted) in duly authorized, validly issued, fully paid and non-assessable shares of common stock at the Conversion Price then in effect. The dividends accrue daily commencing on the issuance date, April 16, 2026.

Voting rights: Holders of Series B Convertible Preferred Stock are entitled to vote upon, in the same manner and with the same effect as the holders of the Company’s common stock, voting together with the holders of the Company’s common stock as a single class. Each share of Series B Convertible Preferred Stock entitle the holder thereof to cast that number of votes per share of Series B Convertible Preferred Stock as is equal to the stated value of the Series B Convertible Preferred Stock, divided by the Conversion Price, and subject to adjustments for any stock splits, stock dividends, stock combinations, recapitalizations or other similar transactions.

5.In ~~Common~~connection ~~Stock~~with the Purchase Agreement, the Company and the Buyer entered into a voting agreement, pursuant to which the Buyer has agreed to vote in favor of matters as related to the proposed Merger at any annual or special meeting and other matters the Company’s board of directors of has recommended the stockholders to vote in favor of.

InThe ~~May~~Company ~~2021,~~evaluated the ~~Company~~classification ~~entered~~of ~~into an At-The-Market Sales Agreement (~~the ~~“Sales~~Series ~~Agreement”)~~B ~~with~~Convertible ~~H.C.~~Preferred ~~Wainwright~~Stock and ~~Co., LLC~~determined ~~(“HCW”)~~equity toclassification ~~act~~was asappropriate due ~~the Company’s sales agent with respect~~ to ~~the~~no ~~issuance~~mandatory ~~and~~or ~~sale~~contingently ofredeemable upredemption ~~to $20~~features.0 ~~million~~Although of the ~~Company’s~~ preferred shares ofwere ~~common~~not ~~stock,~~yet ~~from~~delivered ~~time~~ to ~~time in an at-~~the~~-market~~ ~~public offering (the “ATM Offering”). Upon~~Buyer ~~filing~~as of ~~the~~March ~~Annual~~31, ~~Report~~2026, the Company ~~continued~~concluded tothat bea ~~subject~~firm tocommitment ~~General~~existed ~~Instruction~~as ~~I.B.6~~ of ~~Form~~that ~~S-3~~date, ~~pursuant~~and totherefore ~~which in no event will~~ the ~~Company~~Series ~~sell~~B ~~its~~Convertible ~~common stock in a registered primary offering using Form S-3 with a value exceeding more than one-third of~~Preferred ~~its~~Stock ~~public~~is ~~float~~reported inon ~~any~~the 12balance ~~calendar~~sheet ~~month period so long~~ as ~~its~~of ~~public~~March ~~float remains below $75~~31,~~000,000.~~ ~~Therefore~~2026, ~~the~~net ~~amount~~of ~~that~~$50 ~~the Company~~thousand ~~may~~of beissuance ~~able~~costs toincurred bein ~~raise~~connection ~~using~~with the ~~ATM Offering will be significantly less than $20,000,000, until such time as the Company’s~~Purchase ~~public float held by non-affiliates exceeds $75,000,000~~Agreement.

Pursuant to the Purchase Agreement, prior to the date of the consummation of the Merger, the Company shall be permitted to use up to $250 thousand of the net proceeds for working capital and other general corporate purposes and shall not use the remainder of the net proceeds, subject to certain exceptions. From and after the date of the consummation of the Merger, or upon any termination of the Merger Agreement in accordance with its terms, these restrictions no longer apply. Accordingly, the Company reported $700 thousand of the net proceeds as restricted cash on the accompanying balance sheet as of March 31, 2026.

6. Common Stock

In May 2021, the Company entered into an At-The-Market Sales Agreement (the “Sales Agreement”) with H.C. Wainwright and Co., LLC (“HCW”) to act as the Company’s sales agent with respect to the issuance and sale of up to $20.0 million of the Company’s shares of common stock, from time to time in an at-the-market public offering (the “ATM Offering”). Upon filing of the Annual Report, the Company continued to be subject to General Instruction I.B.6 of Form S-3, pursuant to which in no event will the Company sell its common stock in a registered primary offering using Form S-3 with a value exceeding more than one-third of its public float in any 12 calendar month period so long as its public float remains below $75,000,000. Therefore, the amount that may be able to be raised using the ATM Offering will be significantly less than $20,000,000, until such time as the Company’s public float held by non-affiliates exceeds $75,000,000.

Sales of common stock under the Sales Agreement are made pursuant to an effective shelf registration statement on Form S-3, which was filed with the SEC on May 17, 2024, and subsequently declared effective on May 30, 2024 (File No. 333-279491), and a related prospectus. HCW acts as the Company’s sales agent on a commercially reasonable efforts basis, consistent with its normal trading and sales practices and applicable state and federal laws, rules and regulations and the rules of The Nasdaq Capital Market. If expressly authorized by the Company, HCW may also sell the Company’s common stock in privately negotiated transactions. There is no specific date on which the ATM Offering will end, there are no minimum sale requirements and there are no arrangements to place any of the proceeds of the ATM Offering in an escrow, trust or similar account. HCW is entitled to compensation at a fixed commission rate of 3.0% of the gross proceeds from the sale of the Company’s common stock pursuant to the Sales Agreement.

During the ~~nine~~three months ended ~~September~~March 3031, ~~2025~~2026, and ~~2024~~2025, no shares of the Company’s common stock were sold under the Sales Agreement.

67. Warrants

There were no warrants issued or exercised during the ~~nine~~three months ended ~~September~~March 3031, ~~2025~~2026. During the ~~nine~~three months ended ~~September~~March 3031, ~~2025~~2026, ~~warrants~~ warrants to purchase up to ~~551~~65,~~785~~003 shares of common stock at a weighted-average exercise price of $7949.1599 per share expired. The following ~~represents~~ represents a summary of the warrants outstanding and exercisable at ~~September~~March 3031, ~~2025~~2026, all of which are equity-classified:

Issue Date	Adjusted Exercise Price		Expiration Date	Number of Shares Underlying Warrants
December 17, 2021	$	14.99	December 15, 2026		36,538
December 17, 2021	$	13.99	December 17, 2026		281,047
February 16, 2021	$	49.99	February 11, 2026		65,003
Total					317,585
Total					382,588

7. Stock-based Compensation

The Company sponsored the Pulmatrix, Inc. Amended and Restated 2013 Employee, Director and Consultant Equity Incentive Plan (the “Incentive Plan”), which expired on June 10, 2025. No new awards may be made under the Incentive Plan after its expiration date. Awards issued under the Incentive Plan prior to its expiration remain outstanding in accordance with their terms.

~~There were no options granted or exercised during the nine months ended September 30, 2025~~8. ~~The following table summarizes stock options outstanding~~ asStock-based ~~of September 30, 2025:~~Compensation

No stock options were granted or exercised during the three months ended March 31, 2026. The following table summarizes stock option activity for the three months ended March 31, 2026:

Schedule of Stock Option Activity

	Number of Options			Weighted- Average Exercise Price		Weighted- Average Remaining Contractual Term (Years)		Aggregate Intrinsic Value
Outstanding — January 1, 2025		34,046		$	30.55
Outstanding — January 1, 2026		33,858		$	17.67				-
Forfeited or expired		(188	)	$	2,350.64
Forfeited, cancelled and expired		(1,569	)	$	48.53
Outstanding — September 30, 2025		33,858		$	17.67		5.98	$	10
Outstanding — March 31, 2026		32,289		$	16.17		5.54	$	-
Exercisable — September 30, 2025		29,780		$	19.49		5.81	$	7
Exercisable — March 31, 2026		30,136		$	17.04		5.45	$	-

The Company records stock-based compensation expense related to stock options based on their grant-date fair value. As of ~~September~~March 3031, ~~2025~~2026, there was an immaterial amount of unrecognized stock-based compensation expense related to unvested stock options granted under the Incentive Plan. During the three months ended March 31, 2026, and 2025, the Company’s recognized $3 thousand and $8 thousand of stock-based compensation ~~Incentive~~expense, ~~Plan~~all of which was classified within general and administrative expense.

~~The~~9. ~~following~~Commitments ~~table presents total stock-based compensation expense for the three~~ and ~~nine months ended September 30, 2025, and 2024:~~Contingencies

Schedule of Stock-Based Compensation Expenses

	2025		2024		2025		2024
	Three Months Ended September 30,				Nine months Ended September 30,
	2025		2024		2025		2024
Research and development	$	-		3		-		148
General and administrative		6		194		20		350
Total stock-based compensation expense	$	6		197		20		498

8. Commitments and Contingencies

Research and Development Activities

The Company ~~contracts~~has contracted with various other organizations to conduct research and development activities, including clinical trials. The ~~scope~~ scope of the services under contracts for research and development activities may be modified and the contracts, subject to certain conditions, may generally be cancelled by the Company upon written notice. In some instances, the contracts, subject to certain conditions, may be cancelled by the third party. As of ~~September~~March 3031, ~~2025~~2026, the Company had no material noncancellable commitments.

Legal Proceedings

In the ordinary course of its business, the Company may be involved in various legal proceedings involving contractual and employment relationships, patent or other intellectual property rights, and a variety of other matters. The Company is not aware of any pending legal proceedings that would reasonably be expected to have a material impact on the Company’s financial position or results of operations.

910. Income Taxes

The Company had no income tax expense for the three ~~and nine~~ months ended ~~September~~March 3031, ~~2025~~2026, and ~~2024~~2025 due to operating losses incurred since inception.

Management of the Company evaluated the positive and negative evidence bearing upon the realizability of its deferred tax assets and determined that it is more likely than not that the Company will not recognize the benefits of the deferred tax assets. As a result, a full valuation allowance was recorded as of ~~September~~March 3031, ~~2025~~2026, and December 31, ~~2024~~2025.

The Company applies FASB Accounting Standards Codification 740, Income Taxes, for the financial statement recognition, measurement, presentation, and disclosure of uncertain tax positions taken or expected to be taken in income tax returns. Unrecognized tax benefits represent tax positions for which reserves have been established. A full valuation allowance has been provided against the Company’s deferred tax assets, so that the effect of the unrecognized tax benefits is to reduce the gross amount of the deferred tax asset and the corresponding valuation allowance. The Company has no material uncertain tax positions as of ~~September~~March 3031, ~~2025~~2026, and December 31, ~~2024~~ 2025.

1011. Net Loss Per Share

Basic and diluted net loss per share are computed using the two-class method, which is ~~calculated~~an byearnings ~~dividing~~allocation ~~net~~method ~~loss~~that bydetermines ~~the~~earnings (loss) ~~weighted-average~~per ~~number~~share offor common ~~shares~~and ~~outstanding~~participating ~~during~~securities, which include the ~~period~~Series B Convertible Preferred Stock and certain warrants. ~~Diluted~~Undistributed ~~loss~~earnings ~~per~~are ~~share~~allocated isbetween ~~calculated~~common byshares ~~dividing~~and ~~net~~participating ~~loss~~securities byas ~~the~~if ~~weighted-average~~all ~~number~~earnings ~~common~~had ~~shares~~been ~~outstanding~~distributed during the period~~, after~~. ~~taking~~In ~~into~~periods ~~consideration~~of ~~any~~loss, ~~potentially~~no ~~dilutive~~allocation ~~effects~~is ~~from~~made ~~outstanding~~to ~~stock~~the ~~options~~participating ~~or warrants~~securities.

Basic ~~and diluted net~~ loss per share ~~were~~is ~~the~~then ~~same~~calculated ~~for~~by ~~the~~dividing ~~three~~net ~~and~~loss ~~nine~~by ~~months~~the ~~ended~~weighted-average ~~September~~number ~~30,~~of ~~2025,~~common ~~and~~shares ~~2024,~~outstanding asduring the ~~effect~~period. Diluted ofloss ~~potentially dilutive~~per ~~securities~~share ~~would~~is ~~have~~calculated ~~been~~by ~~anti-dilutive.~~dividing ~~The~~net ~~following~~loss ~~potentially~~by ~~dilutive~~the ~~securities~~weighted-average ~~outstanding~~number ~~have~~common ~~been~~shares ~~excluded~~outstanding ~~from~~ during the ~~computation~~period, after oftaking ~~diluted~~into ~~weighted-average~~consideration ~~shares~~any ~~outstanding,~~potentially ~~because~~dilutive ~~such~~effects ~~securities~~from ~~had~~outstanding anconvertible ~~anti-dilutive~~instruments, ~~impact:~~stock options or warrants.

Basic and diluted net loss per share were the same for the three months ended March 31, 2026, and 2025, as the effect of potentially dilutive securities would have been anti-dilutive. The following potentially dilutive securities outstanding have been excluded from the computation of diluted weighted-average shares outstanding, because such securities had an anti-dilutive impact. The Series B Convertible Preferred Stock is not included as potentially dilutive securities because they were not yet outstanding as of March 31, 2026.

	Three and Nine Months Ended September 30,
	Three Months Ended March 31,
	2025		2024
	2026		2025
Options to purchase common stock		3332,~~858~~289		~~250~~34,~~897~~046
Warrants to purchase common stock		~~382~~317,~~588~~585		934,373
Total options and warrants to purchase common stock		416,446		1,185,270
Total potentially dilutive securities excluded		349,874		968,419

1112. Segment Reporting

The Company operates in a single reportable segment. The accounting policies of the segment are the same as those applicable to the Company. The measure of segment assets is reported on the balance sheet as total consolidated assets.

The Company’s chief operating decision maker (“CODM”) is its chief executive officer, who reviews financial information presented on a consolidated basis. The CODM uses net loss to assess financial performance of the Company and allocate resources, in addition to operating forecasts and clinical results.

The Company’s ~~single segment revenue,~~ significant segment expenses, and other segment items and net loss are each presented separately on the Company’s consolidated statements of operations.

1213. Subsequent Events

The Company has completed an evaluation of all subsequent events after the balance sheet date of ~~September~~March 3031, ~~2025~~2026, through the date the ~~condensed~~ condensed consolidated financial statements were issued to ensure that the condensed consolidated financial statements include appropriate ~~disclosure~~ disclosure of events both recognized in the condensed consolidated financial statements as of ~~September~~March 3031, ~~2025~~2026, and events which occurred ~~subsequently~~ subsequently but were not recognized in the condensed consolidated financial statements. The Company has ~~concluded~~determined that no ~~other subsequent~~ events ~~have~~requiring ~~occurred~~recognition or ~~that require~~ disclosure, ~~except~~exist asother ~~disclosed~~than ~~within~~those ~~the~~already ~~condensed~~disclosed ~~consolidated financial statements~~herein.

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

Management’s Discussion and Analysis of Financial Condition and Results of Operations is intended to provide a reader of our financial statements with a narrative from the perspective of our management on our financial condition, results of operations, liquidity, and certain other factors that may affect our future results. The information set forth below should be read in conjunction with the condensed consolidated financial statements and the notes thereto included elsewhere in this Quarterly Report on Form 10-Q, as well as the audited consolidated financial statements and the notes thereto contained in our Annual Report on Form 10-K ~~filed~~for the fiscal year ended December 31, 2025, filed with the SEC on ~~March~~February 2126, ~~2025~~2026 (the “Annual Report”). Unless stated otherwise, references in this Quarterly Report on Form 10-Q to “us,” “we,” “our,” or our “Company” and similar terms refer to Pulmatrix, Inc., a Delaware corporation and its subsidiaries.

Forward-Looking Statements

This Quarterly Report on Form 10-Q contains forward-looking statements. All statements other than statements of historical fact contained herein, including statements regarding our business plans or strategies, projected or anticipated benefits or other consequences of our plans or strategies, projected or anticipated benefits from acquisitions to be made by us, or projections involving anticipated revenues, earnings, or other aspects of our operating results, are forward-looking statements. Words such as “anticipates,” “assumes,” “believes,” “can,” “could,” “estimates,” “expects,” “forecasts,” “guides,” “intends,” “is confident that,” “may,” “plans,” “seeks,” “projects,” “targets,” and “would,” and their opposites and similar expressions, as well as statements in future tense, are intended to identify forward-looking statements. Forward-looking statements should not be read as a guarantee of future performance or results and may not be accurate indications of when such performance or results will actually be achieved. Forward-looking statements are based on information we have when those statements are made or our management’s good faith belief as of that time with respect to future events and are subject to risks and uncertainties that could cause actual performance or results to differ materially from those expressed in or suggested by the forward-looking statements. Important factors that could cause such differences include, but are not limited to:

● the risk that the conditions to closing ~~(the “Closing”)~~ of the potential Merger with ~~Cullgen~~Eos (each as defined herein) are not satisfied, including failure to obtain ~~applicable~~stockholder ~~regulatory~~approval ~~approvals~~ for the transactions; ● our ability to continue as a going concern; ● the risk that we are unable to meet expectations regarding the timing and completion of the Merger; ● uncertainties as to the timing and costs of the consummation of the transactions contemplated by the Merger Agreement (as defined herein); ● the occurrence of any event, change or other circumstance or condition that could give rise to the termination of the Merger Agreement; ● the ~~risk that the Merger Agreement may be terminated in circumstances that require us to pay a termination fee; ● the~~ outcome of any legal proceedings that may be instituted against us, ~~Cullgen~~Eos, or any of each company’s respective directors or officers related to the Merger Agreement or the transactions contemplated thereby; ● should we resume development of our product candidates, our history of recurring losses and negative cash flows from operating activities, significant future commitments and the uncertainty regarding the adequacy of our liquidity to pursue or complete our business objectives; ● should we resume development of our product candidates, our inability to carry out research, development and commercialization plans; ● should we resume development of our product candidates, our inability to manufacture our product candidates on a commercial scale on our own or in collaborations with third parties; ● should we resume development of our product candidates, our inability to complete preclinical testing and clinical trials as anticipated;

● should we resume development of our product candidates, our collaborators’ inability to ~~complete~~successfully ~~preclinical~~carry ~~testing~~out ~~and~~their ~~clinical~~contractual ~~trials~~duties; as● ~~anticipated~~should we resume development of our product candidates, termination of certain license agreements; ● should we resume development of our product candidates, our ~~collaborators’~~ability ~~inability~~to adequately protect and enforce rights to ~~successfully~~intellectual ~~carry~~property, ~~out~~or ~~their~~defend ~~contractual~~against ~~duties~~claims of infringement by others; ● should we resume development of our product candidates, ~~termination~~difficulties ofin ~~certain~~obtaining ~~license~~financing ~~agreements~~on commercially reasonable terms, or at all; ● should we resume development of our product candidates, intense competition in our ~~ability~~industry, towith ~~adequately~~competitors ~~protect~~having substantially greater financial, technological, research and ~~enforce~~development, ~~rights~~regulatory toand ~~intellectual~~clinical, ~~property~~manufacturing, ormarketing ~~defend~~and ~~against~~sales, ~~claims~~distribution, personnel and resources than we do; ● should we resume development of ~~infringement~~our byproduct ~~others~~candidates, entry of new competitors and products and potential technological obsolescence of our products; ● adverse market and economic conditions; ● our ability to maintain compliance with the listing standards of the Nasdaq Capital Market (“Nasdaq”); ● ~~economic~~loss ~~and~~of ~~market~~one ~~conditions~~or more key executives; and ● should we resume development of our product candidates, difficulties in ~~obtaining~~securing ~~financing~~regulatory onapproval ~~commercially~~to ~~reasonable~~market ~~terms,~~our orproduct ~~at all~~candidates.

For a more detailed discussion of these and other risks that may affect our business and that could cause our actual results to differ from those projected in these forward-looking statements, see the risk factors and uncertainties described under the heading “Risk Factors” in Part II, Item 1A of this Quarterly Report on Form 10-Q and in Part I, Item 1A of our Annual Report on Form 10-K. The forward-looking statements contained in this Quarterly Report on Form 10-Q are expressly qualified in their entirety by this cautionary statement. We do not undertake any obligation to update any forward-looking statement to reflect events or circumstances after the date on which any such statement is made or to reflect the occurrence of unanticipated events, except as required by law.

“iSPERSE^™” is one of our trademarks used in this Quarterly Report on Form 10-Q. Other trademarks appearing in this report are the property of their respective holders. Solely for convenience, these and other trademarks, trade names and service marks referred to in this report appear without the ^®, TM and SM symbols, but those references are not intended to indicate, in any way, we or the owners of such trademarks will not assert, to the fullest extent under applicable law, their rights to these trademarks and trade names.

Overview

Business

We are a biopharmaceutical company that has focused on the development of novel inhaled therapeutic products intended to prevent and treat migraine and respiratory diseases with important unmet medical needs using our patented iSPERSE™ technology. Our proprietary product pipeline includes treatments for central nervous system (“CNS”) disorders such as acute migraine and serious lung diseases such as Chronic Obstructive Pulmonary Disease (“COPD”) and allergic bronchopulmonary aspergillosis (“ABPA”). Our product candidates are based on our proprietary engineered dry powder delivery platform, iSPERSE™, which seeks to improve therapeutic delivery to the lungs by optimizing pharmacokinetics and reducing systemic side effects to improve patient outcomes.

We design and develop inhaled therapeutic products based on our proprietary dry powder delivery technology, iSPERSE™, which enables delivery of small or large molecule drugs to the lungs by inhalation for local or systemic applications. The iSPERSE™ powders are engineered to be small, dense particles with highly efficient dispersibility and delivery to airways. iSPERSE™ powders can be used with an array of dry powder inhaler technologies and can be formulated with a broad range of drug substances including small molecules and biologics. We believe the iSPERSE™ dry powder technology offers enhanced drug loading and delivery efficiency that outperforms traditional lactose-blend inhaled dry powder therapies.

We believe the advantages of using the iSPERSE™ technology include reduced total inhaled powder mass, enhanced dosing efficiency, reduced cost of goods, and improved safety and tolerability profiles.

13After a comprehensive review of strategic alternatives, including identifying and reviewing potential candidates for a strategic transaction, on March 26, 2026, we and Eos SENOLYTIX, Inc., a Delaware corporation (“Eos”), entered into an Agreement and Plan of Merger and Reorganization (the “Merger Agreement”), pursuant to which, among other matters, PUOS Merger Sub, Inc., our wholly owned subsidiary (“Merger Sub”), will merge with and into Eos, with Eos continuing as the surviving corporation and our wholly owned subsidiary (the “Merger”).

~~After~~The aconsummation ~~comprehensive review~~ of ~~strategic~~the ~~alternatives,~~Merger ~~including~~is ~~identifying~~subject ~~and~~to ~~reviewing~~approval ~~potential~~by ~~candidates~~our ~~for~~stockholders ~~a strategic transaction, on November 13, 2024, we entered into the Agreement~~ and ~~Plan~~Eos ~~of Merger and Reorganization~~stockholders, as ~~amended~~well byas ~~Amendment~~other ~~No.~~customary 1closing ~~(“Amendment~~conditions, ~~No.~~including ~~1”)~~the ~~thereto~~effectiveness onof ~~April~~a 7,registration ~~2025~~statement ~~(as~~filed ~~amended~~with bythe ~~Amendment~~Securities ~~No.~~and 1,Exchange ~~the~~Commission (“~~Merger Agreement~~SEC”), ~~pursuant~~in ~~to which, among~~connection ~~other~~with ~~matters,~~the ~~PCL~~transaction ~~Merger~~and ~~Sub,~~Nasdaq’s ~~Inc.,~~approval ~~our~~of ~~direct~~the ~~wholly~~listing ~~owned~~of ~~subsidiary,~~the ~~will~~shares ~~merge~~of ~~with and into Cullgen Inc. (“Cullgen”), with Cullgen surviving as~~ our ~~wholly~~common ~~owned~~stock ~~subsidiary~~to ~~and~~be ~~the~~issued ~~surviving~~in ~~corporation~~connection ofwith the Merger. ~~merger~~If (the “Merger~~”).~~ ~~The~~is ~~Merger Agreement~~completed, ~~was~~the ~~unanimously~~business ~~approved by our board~~ of ~~directors,~~Eos ~~which~~will ~~resolved~~continue toas ~~recommend~~the ~~approval~~business of the ~~Merger~~combined ~~Agreement to our stockholders~~company.

OnOur ~~June~~future ~~16,~~operations ~~2025,~~are wehighly ~~held~~dependent aon ~~special~~the ~~meeting~~success ~~in lieu~~ of the ~~annual~~Merger ~~meeting~~and ofthere ~~Pulmatrix~~can ~~stockholders,~~be atno ~~which~~assurances ~~special~~that ~~meeting our stockholders approved~~ the Merger ~~and~~will ~~related~~be ~~proposals~~successfully consummated. ~~The~~There ~~Closing~~can isbe ~~subject~~no toassurance ~~other~~that ~~customary closing conditions, including Nasdaq’s approval of~~ the ~~listing~~strategic ofreview ~~the~~process ~~shares~~or ofany ~~Pulmatrix~~transaction ~~common~~relating ~~stock~~ to bea ~~issued~~specific inasset, ~~connection~~including ~~with~~ the Merger and ~~approval~~any ~~from~~asset ~~the~~development ~~China~~or ~~Security Regulatory~~sale, ~~Commission~~will ~~(“CSRC”)~~result ~~pursuant~~in tous ~~the~~pursuing ~~Trial~~such ~~Administrative~~a ~~Measures~~transaction, ofor ~~Overseas~~that ~~Securities~~any ~~Offering and Listing by Domestic Enterprises (the “Trial Measures”)~~transactions, ~~No.~~if ~~1 to No. 6 Supporting Guidance Rules~~pursued, ~~the~~will ~~Notice on Administration Arrangements~~be ~~for~~completed ~~the Filing of Overseas Listings by Domestic Enterprises and the relevant CSRC Answers to Reporter Questions~~ on ~~the~~terms ~~official~~favorable ~~website of the CSRC. These regulations established a filing-based regime~~ to ~~regulate~~us ~~overseas offerings~~ and ~~listings~~our bystockholders ~~Chinese~~in ~~domestic companies. As of~~ the ~~date~~existing ofPulmatrix ~~this~~entity ~~filing,~~or weany ~~have~~possible ~~not~~entity ~~yet~~that ~~received~~results ~~approval~~ from ~~the~~a ~~CSRC~~combination of toentities. ~~complete~~If the ~~Merger.~~ Asstrategic ~~previously~~review ~~disclosed,~~process onis ~~August 1~~unsuccessful, ~~2025, we~~ and ~~Cullgen,~~if ~~as provided for in~~ the Merger ~~Agreement,~~is ~~mutually~~not ~~agreed to extend the “End Date”~~consummated, ~~a term defined in~~ the ~~Merger~~Pulmatrix ~~Agreement,~~board byof 60directors may ~~days~~decide ~~from August 13, 2025,~~ to ~~October~~pursue ~~12, 2025. The Merger Agreement does not have~~ a ~~defined~~dissolution ~~term~~ and ~~does~~liquidation ~~not~~of ~~terminate on~~ the ~~“End Date”~~Company. ~~The “End Date” is simply the date at which certain termination options become available to either party.~~

If the Merger is completed, the business of Cullgen will continue as the business of the combined company. We are currently seeking opportunities to monetize iSPERSE™ and our existing clinical assets.

Our future operations are highly dependent on the success of the Merger and there can be no assurances that the Merger will be successfully consummated. There can be no assurance that the strategic review process or any transaction relating to a specific asset, including the Merger and any asset sale, will result in us pursuing such a transaction, or that any transactions, if pursued, will be completed on terms favorable to us and our stockholders in the existing Pulmatrix entity or any possible entity that results from a combination of entities. If the strategic review process is unsuccessful, and if the Merger is not consummated, the Pulmatrix board of directors may decide to pursue a dissolution and liquidation of the Company.

Our goal has been to develop breakthrough therapeutic products that are safe, convenient, and more effective than the existing therapeutic products for respiratory and other diseases where iSPERSE™ properties are advantageous.

Our current pipeline of clinical assets is aligned to this goal and includes iSPERSE™-based therapeutic candidates, which target the prevention and treatment of a range of diseases, including CNS disorders and pulmonary diseases. These therapeutic candidates include PUR3100 for the treatment of acute migraine, PUR1800 for the treatment of acute exacerbations of chronic obstructive pulmonary disease (“AECOPD”), and PUR1900 for the treatment of ABPA in patients with asthma and in patients with cystic fibrosis. Each program is enabled by its unique iSPERSE™ formulation designed to achieve specific therapeutic objectives.

InWe ~~connection~~are ~~with~~continuing ~~the~~to ~~Merger,~~explore ~~we are exploring~~ opportunities to monetize these clinical assets and have paused the development of these product candidates. Continued development of these candidates, if that were to occur, would be contingent on securing additional funding and would require significant expenditures to advance. Thereafter, if development of such product candidates were to be continued and successfully advanced (of which there can be no assurance), it would be necessary to seek and obtain marketing approval to commercialize such product candidates, which could be expected to require the expenditure of significant additional resources and expenses related to regulatory, product sales, medical affairs, marketing, manufacturing and distribution.

Contingent on securing additional funding and continuing development of these candidates, we would expect to continue to incur substantial expenses and operating losses for at least the next several years, as we would:

● Pursue further clinical studies for PUR3100, an orally inhaled dihydroergotamine (“DHE”) including a Phase 2 clinical study for the treatment of acute migraine. We received Food and Drug Administration (“FDA”) acceptance of our Investigational New Drug Application (“IND”) and a “study may proceed” letter in September 2023, positioning PUR3100 as Phase 2-ready for potential financing or partnership discussions.

WeContingent on ~~developed~~securing ~~PUR3100,~~additional anfunding ~~iSPERSE™ formulation of DHE in 2020. We completed good laboratory practice (“GLP”) toxicology studies in 2021~~ and ~~2022.~~continuing Indevelopment ~~2022, we completed a Phase 1 study designed as a double-blinded trial to assess the safety, tolerability, and pharmacokinetics~~ of ~~three~~these ~~dose levels of single doses of inhaled PUR3100 with intravenous (“IV”) placebo~~candidates, ~~as compared to IV DHE (DHE mesylate injection) with inhaled placebo. On January 4, 2023,~~ we ~~announced~~would ~~the~~expect ~~Phase 1 topline results, indicating that PUR3100 was safe and tolerated with fewer gastrointestinal side effects in all doses compared~~ to IVcontinue DHE. PUR3100 showed a five-minute Tmax and Cmax within the targeted therapeutic range for all three doses tested. The Phase 1 study data was presented at the American Headache Society 65th Annual Meeting in June 2023. In May 2024, we announced a peer-reviewed publication of Phase 1 clinical results in the publication Headache: The Journal of Head and Face Pain. In September 2023, we announced the FDA’s acceptance of an IND application for PUR3100 and receipt of a “study may proceed” letter for a Phase 2 study. The IND includes a Phase 2 clinical protocol where safety and preliminary efficacy of PUR3100 will be investigated in patients with acute migraine. Based on the rapid systemic exposure in the therapeutic range and the improved side effect profile relative to IVincur ~~dosing,~~substantial we believe the PUR3100 formulation of DHE may differentiate from approved DHE products or those in development. If effectiveness is demonstrated, PUR3100 may offer the convenience of being self-administered with a pharmacokinetic profile that may potentially provide rapid onset of action. ● Pursue partnership or other alternatives to monetize or advance PUR1800, focusing on the development of an orally inhaled kinase inhibitor for treatment of AECOPD. We completed preclinical safety studies for PUR1800, our iSPERSE™ formulation of RV1162, in 2018 expenses and ~~advanced~~operating ~~our~~losses formulation and process development efforts to support clinical testing in stable moderate-severe COPD patients. We completed a Phase 1b safety, tolerability, and pharmacokinetics clinical study of PUR1800 for subjects with stable moderate-severe COPD and received topline data from the Phase 1b clinical study in the first quarter of 2022. We analyzed data from the completed Phase 1b clinical study of PUR1800 for AECOPD and presented study results at ~~the~~least ~~American Academy of Allergy, Asthma & Immunology (AAAAI) conference in~~ the ~~first~~next ~~quarter~~several ~~of 2023. The results indicated PUR1800 was safe and well tolerated with no observed safety signals. The topline data~~years, ~~along~~as with the results from chronic toxicology studies, support the continued development of PUR1800 for the treatment of AECOPD and other inflammatory respiratory diseases. ● Capitalize on our proprietary iSPERSE™ technology and our expertise in inhaled therapeutics and particle engineering to identify new product candidates for prevention and treatment of diseases, including those with important unmet medical needs. To add additional inhaled therapeutics to our development pipeline and facilitate additional collaborations, we are leveraging our iSPERSE™ technology and our expertise in inhaled therapeutics and particle engineering to identify potential product candidates. ● Invest in protecting and expanding our intellectual property portfolio and file for additional patents to strengthen our intellectual property rights.would:

●

Pursue further clinical studies for PUR3100, an orally inhaled dihydroergotamine (“DHE”) including a Phase 2 clinical study for the treatment of acute migraine. We received Food and Drug Administration (“FDA”) acceptance of our Investigational New Drug Application (“IND”) and a “study may proceed” letter in September 2023, positioning PUR3100 as Phase 2-ready for potential financing or partnership discussions.

We developed PUR3100, an iSPERSE™ formulation of DHE in 2020. We completed good laboratory practice (“GLP”) toxicology studies in 2021 and 2022. In 2022, we completed a Phase 1 study designed as a double-blinded trial to assess the safety, tolerability, and pharmacokinetics of three dose levels of single doses of inhaled PUR3100 with intravenous (“IV”) placebo, as compared to IV DHE (DHE mesylate injection) with inhaled placebo.

On January 4, 2023, we announced the Phase 1 topline results, indicating that PUR3100 was safe and tolerated with fewer gastrointestinal side effects in all doses compared to IV DHE. PUR3100 showed a five-minute T_max and C_max within the targeted therapeutic range for all three doses tested. The Phase 1 study data was presented at the American Headache Society 65th Annual Meeting in June 2023. In May 2024, we announced a peer-reviewed publication of Phase 1 clinical results in the publication Headache: The Journal of Head and Face Pain.

		In September 2023, we announced the FDA’s acceptance of an IND application for PUR3100 and receipt of a “study may proceed” letter for a Phase 2 study. The IND includes a Phase 2 clinical protocol where safety and preliminary efficacy of PUR3100 will be investigated in patients with acute migraine. Based on the rapid systemic exposure in the therapeutic range and the improved side effect profile relative to IV dosing, we believe the PUR3100 formulation of DHE may differentiate from approved DHE products or those in development. If effectiveness is demonstrated, PUR3100 may offer the convenience of being self-administered with a pharmacokinetic profile that may potentially provide rapid onset of action.

	●	Pursue partnership or other alternatives to monetize or advance PUR1800, focusing on the development of an orally inhaled kinase inhibitor for treatment of AECOPD.

		We completed preclinical safety studies for PUR1800, our iSPERSE^™ formulation of RV1162, in 2018 and advanced our formulation and process development efforts to support clinical testing in stable moderate-severe COPD patients. We completed a Phase 1b safety, tolerability, and pharmacokinetics clinical study of PUR1800 for subjects with stable moderate-severe COPD and received topline data from the Phase 1b clinical study in the first quarter of 2022. We analyzed data from the completed Phase 1b clinical study of PUR1800 for AECOPD and presented study results at the American Academy of Allergy, Asthma & Immunology (AAAAI) conference in the first quarter of 2023. The results indicated PUR1800 was safe and well tolerated with no observed safety signals. The topline data, along with the results from chronic toxicology studies, support the continued development of PUR1800 for the treatment of AECOPD and other inflammatory respiratory diseases. In 2024, Pulmatrix published an abstract titled “Ex vivo evaluation of the potential for Narrow Spectrum Kinase inhibitors as a treatment for Idiopathic Pulmonary Fibrosis”.

	●	Capitalize on our proprietary iSPERSE™ technology and our expertise in inhaled therapeutics and particle engineering to identify new product candidates for prevention and treatment of diseases, including those with important unmet medical needs.

		To add additional inhaled therapeutics to our development pipeline and facilitate additional collaborations, we are leveraging our iSPERSE™ technology and our expertise in inhaled therapeutics and particle engineering to identify potential product candidates.

		The status of our patent portfolio changes frequently in the ordinary course of patent prosecution. As of September 30, 2025, our patent portfolio related to iSPERSE™ included approximately 146 granted patents, 18 of which are granted US patents, with expiration dates from 2026 to 2043, and approximately 50 additional pending patent applications in the US and other jurisdictions. Our in-licensed portfolio related to kinase inhibitors included approximately 283 granted patents, 33 of which are granted US patents, with expiration dates from 2029 to 2035, and approximately 14 additional pending patent applications in the US and other jurisdictions. We have national phase applications pending in Australia, Brazil, Canada, China, Europe, Israel, India, Japan, Korea, Mexico, New Zealand, Russia, and the United States that cover certain formulations and methods of use relevant to our PUR3100 program.
	●	Invest in protecting and expanding our intellectual property portfolio and file for additional patents to strengthen our intellectual property rights.
		The status of our patent portfolio changes frequently in the ordinary course of patent prosecution. As of March 31, 2026, our patent portfolio related to iSPERSE™ included approximately 146 granted patents, 18 of which are granted US patents, with expiration dates from 2026 to 2043, and approximately 48 additional pending patent applications in the US and other jurisdictions. Our in-licensed portfolio related to kinase inhibitors included approximately 285 granted patents, 33 of which are granted US patents, with expiration dates from 2029 to 2035, and approximately 8 additional pending patent applications in the US and other jurisdictions. We have national phase applications pending in Australia, Brazil, Canada, China, Europe, Israel, India, Japan, Korea, Mexico, New Zealand, Russia, Hong Kong and the United States that cover certain formulations and methods of use relevant to our PUR3100 program.
	●	Seek partnerships and license agreements to support the product development and commercialization of our product candidates.
		In order to advance our clinical programs, we may seek partners or licensees in areas of pharmaceutical and clinical development.
		In order to advance our clinical programs, we may be dependent on seeking partners or licensees in areas of pharmaceutical and clinical development.

Therapeutic Candidates

PUR3100

WePUR3100 is still an investigational drug candidate and not authorized for commercialization, but we are currently exploring ~~opportunities~~other opportunities to monetize PUR3100. All U.S. clinical development is currently on hold while we work to license or monetize this asset.

In 2020, we developed PUR3100, the iSPERSE™ formulation of DHE, for the treatment of acute migraine. Currently DHE is only available as subcutaneous, intravenous infusion or intranasal delivery. If approved for commercialization, PUR3100 has the opportunity to be the first orally inhaled DHE treatment for acute migraine and be an alternative to other acute therapies. Given the oral inhaled ~~route~~ route of delivery, PUR3100 is anticipated to provide rapid relief from ~~the rapid onset of~~ migraine symptoms and provide a favorable tolerability profile.

A total of three 14-day GLP toxicology studies have been completed with PUR3100 to support single-dose clinical studies. We are planning to conduct a chronic toxicology study to support long-term dosing. Based on discussions with the FDA, this would complete the non-clinical requirements to support an NDA.

Our interactions with the FDA have indicated that, inas ~~addition~~part toof Phase 2 and Phase 3 studies, long-term safety should be assessed in a minimum of one hundred patients for six months of dosing and fifty patients for twelve months of dosing. The FDA also confirmed that it will be necessary to perform a safety study administering PUR3100 to otherwise healthy patients with asthma before ana ~~NDA~~new drug application is submitted.

On September 26, 2022, we announced the completion of patient dosing in a Phase 1 clinical study, performed in Australia. The study design was a double-dummy, double-blinded trial to assess the safety, tolerability, and pharmacokinetics of three dose levels of single doses of inhaled PUR3100 with IV placebo, as compared to IV DHE (DHE mesylate injection) with inhaled placebo. This study may also provide preliminary comparative bioavailability data to support the use of the 505(b)(2) pathway for marketing authorization. Twenty-six healthy subjects were enrolled and each of the four groups contained at least six subjects.

On January 4, 2023, we announced topline results. We presented the Phase 1 study data at the American Headache Society 65th Annual Meeting in June 2023. The study showed that PUR3100 achieved peak exposures in the targeted therapeutic range and time to maximum concentration occurred at five minutes after dosing at all dosing levels. The PUR3100 dose groups also showed a lower incidence of nausea and no vomiting compared to observations of nausea and vomiting in the IV administered DHE dose group.

Based on the rapid systemic exposure in the therapeutic range and the improved side effect profile relative to IV dosing, we believe the PUR3100 formulation of DHE may differentiate from approved DHE products or those known to be in development. If effectiveness is demonstrated, PUR3100 may offer the convenience of being self-administered with a pharmacokinetic profile that may potentially provide rapid onset of action.

In September 2023, we announced that the FDA accepted the PUR3100 IND and the receipt of a “study may proceed” letter for the clinical study: “A Phase 2, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Single Event Study to Evaluate the Safety, Tolerability, and Efficacy of PUR3100 (Dihydroergotamine Mesylate Inhalation Powder) in the Acute Treatment of Migraine”. We anticipate that this Phase 2 clinical study will initiate once financing or partnership arrangements have been made.

On May 15, 2024, we announced publication of, “Safety, tolerability, and pharmacokinetics of a single orally inhaled dose of PUR3100, a dry powder formulation of dihydroergotamine versus intravenous dihydroergotamine: A Phase 1 randomized, double-blind study in healthy adults” in the peer-reviewed publication Headache: The Journal of Head and Face Pain.

We believe that in this trial, PUR3100 demonstrated the potential for rapid pain relief and improved DHE tolerability versus IV DHE. With a T_max of 5 minutes and a C_max in the therapeutic window for all doses tested, we believe that PUR3100 has the potential to address an unmet need for acute migraine sufferers and we are pursuing different options to advance PUR3100 into a Phase 2 clinical trial to further investigate its promising profile in treating acute migraine.

The completed Phase 1 study demonstrated optimal pharmacokinetics and improved tolerability of PUR3100 compared to IV DHE. The Phase 1 trial was a randomized, double-dummy, double-blinded design to assesses the safety, tolerability, and pharmacokinetics (PK) of three dose groups treated with inhaled PUR3100 with intravenous (IV) placebo, compared to a single dose of IV DHE (DHE mesylate injection) with inhaled placebo in healthy volunteers. All doses of PUR3100 were generally well tolerated with a lower incidence of nausea (21% vs. 86%), vomiting (0% vs. 29%), and headache (16% vs. 57%) compared to IV DHE. The pharmacokinetic (“PK”) profile of PUR3100 versus IV DHE was characterized by a similar mean time to Cmax (5 vs. 5.5 min), with reduced AUC0–2h (1120–4320 vs. 6340 ng*h/mL), and a lower Cmax (3620–14,400 vs. 45,000 ng/mL). All doses of PUR3100 were associated with mean Cmax above the minimum level required to achieve efficacy (1000 pg/mL).

PUR1800

WePUR1800 is still an investigational drug candidate and not authorized for commercialization, but we are currently exploring ~~opportunities~~other opportunities to monetize PUR1800. All clinical development is currently on hold while we work to license or monetize this asset.

PUR1800 is a Narrow Spectrum Kinase Inhibitor, engineered with our iSPERSE™ technology, ~~being~~with ~~developed~~a target indication for the treatment of of acute exacerbations in chronic obstructive pulmonary disease ~~(AECOPD)~~. PUR1800 targets p38 MAP kinases (p38MAPK), Src kinases, and Syk kinases. These kinases play a critical role in chronic inflammation and airway remodeling.

We completed a Phase 1b safety, tolerability, and pharmacokinetics of PUR1800 ~~for~~in patients with stable moderate-severe COPD. Topline data ~~was~~were delivered in the first quarter of 2022 and presented at the American Academy of Allergy, Asthma and Immunology conference in the first quarter of 2023.

The clinical study, performed at the Medicines Evaluation Unit in Manchester, UK, was a randomized, three-way crossover double-blind study with 14 days of daily dosing, which included placebo and one of two doses of PUR1800, and included a 28-day follow-up period after each treatment period. A total of 18 adults with stable COPD were enrolled. Safety and tolerability, as well as systemic pharmacokinetics ~~(“PK”)~~ were evaluated.

PUR1800 was well tolerated and there were no observed safety signals. The PK data indicate that PUR1800 results in low and consistent systemic exposure when administered via oral inhalation. The topline data, along with the results from chronic toxicology studies, support the continued development of PUR1800 for the treatment of AECOPD and other inflammatory respiratory diseases. These data will inform the design of a potential Phase 2 study in the treatment of AECOPD.

Toxicology studies in rats and dogs, with durations of six and nine months respectively, are complete. The data from both studies demonstrated that PUR1800 is safe and well tolerated with chronic dosing, with little to no progression of findings from 28-day studies. We believe that this indicates potential for chronic dosing of PUR1800, enabling us to explore PUR1800 therapy for chronic respiratory diseases such as steroid resistant asthma, COPD, or idiopathic pulmonary fibrosis. While the program is currently in development for treatment of acute exacerbation of COPD, these positive toxicology study results could expand potential indications and value of the program.

Toxicology studies in rats and dogs, with durations of six and nine months respectively, are complete. The data from both studies demonstrated that PUR1800 is safe and well tolerated with chronic dosing, with little to no progression of findings from 28-day studies. We believe that this indicates potential for chronic dosing of PUR1800, enabling us to explore PUR1800 therapy for chronic respiratory diseases such as steroid resistant asthma, COPD, or idiopathic pulmonary fibrosis. While the program is currently focused on treatment of acute exacerbation of COPD, these positive toxicology study results could expand potential indications and value of the program.

Additionally, in 2024, Pulmatrix published an abstract regarding potential for treatment of IPF titled “Ex vivo evaluation of the potential for Narrow Spectrum Kinase inhibitors as a treatment for Idiopathic Pulmonary Fibrosis”.

PUR1900

WePUR1900 is still an investigational drug candidate and not authorized for commercialization, but we are currently exploring ~~opportunities~~other opportunities to monetize PUR1900 within the United States.

PUR1900 is our iSPERSE^™ inhaled formulation of itraconazole, an antifungal drug commercially available as an oral drug. We developed PUR1900 for the prevention and potential treatment of fungal infections and allergic/hypersensitivity reactions to fungus in patients with severe lung disease, including those with asthma and cystic fibrosis.

On April 15, 2019, we entered into a Development and Commercialization Agreement (the “Cipla Agreement”) with Cipla for the co-development and commercialization, on a worldwide, except for the Cipla Territory defined below, exclusive basis, of PUR1900, our inhaled iSPERSE^™drug delivery system (the “Product”) enabled formulation of the antifungal drug itraconazole, which is only available as an oral drug, for the treatment of all pulmonary indications, including ABPA in patients with asthma. We entered into an amendment to the Cipla Agreement on November 8, 2021 (the “Second Amendment”) and a subsequent amendment on January 6, 2024 (the “Third Amendment”). All references to the Cipla Agreement herein refer to the Cipla Agreement, as amended. The Cipla Agreement will remain in effect in perpetuity, unless otherwise earlier terminated in accordance with its terms.

Pursuant to the Third Amendment, all development and commercialization activities with respect to the Product in all markets other than the United States (the “Cipla Territory”) will be conducted exclusively by Cipla at Cipla’s sole cost and expense, and Cipla shall be entitled to all profits from the sale of the Product in the Cipla Territory, except that we will receive 2% royalties on any potential future net sales by Cipla outside the United States.

Also pursuant to the Third Amendment, we and Cipla stopped patient enrollment for the ongoing Phase 2b clinical study. We agreed that during the period commencing on January 6, 2024 and ending July 30, 2024 (the “Wind Down Period”), we would complete all Phase 2b activities, assign or license all patents to Cipla and their registration with the appropriate authorities in the Cipla Territory, complete a physical and demonstrable technology transfer and secure all data from the Phase 2b study for inclusion in the safety database for the Cipla Territory.

We completed all Phase 2b wind down activities in the third quarter of 2024. As such, we no longer bear further financial responsibility for the commercialization and development with respect to the Product in the Cipla Territory, with such commercialization and development expenses of the Product in the Cipla Territory to be borne at Cipla’s sole cost and expense after January 6, 2024.

Our partner Cipla has continued clinical development outside the United States and India’s Central Drug Standard Control Organization has accepted Cipla’s Phase 2 clinical trial results for inhaled itraconazole dry powder formulation and approved the company’s proposal to proceed with Phase 3 trials. ~~Should~~using ~~Cipla~~a ~~successfully~~40mg ~~market~~dose ~~PUR1900~~of ~~outside the United States~~PUR1900, ~~Pulmatrix~~which ~~will receive 2% royalties on any potential future net sales by~~ Cipla ~~outside~~expects ~~the United States. Within the United States, we and Cipla will seek~~ to ~~monetize PUR1900~~commence ~~for~~in ~~indications where an orally inhaled antifungal may provide a therapeutic benefit or fulfill an unmet medical need~~2026.

~~Financial~~Cipla ~~Overview~~published the results of their Phase 2 trial in the European Respiratory Journal. This was a randomized, double-blind, placebo-controlled trial including subjects with ABPA-complicating asthma. Participants received PUR1900 (20 or 40 mg) or placebo (2:2:1) once daily for 16 weeks. Efficacy endpoints included FEV1, asthma control (ACQ-7), serum total IgE, and quality of life (AQLQ).

Revenues

To date, we have not generated any product sales. No revenues were recognized for the nine months ended September 30, 2025, and the revenues for the three and nine months ended September 30, 2024, were primarily generated from the Cipla Agreement as related to our PUR1900 program, for which wind down activities have been completed.

Regarding results, forty-three subjects (mean age 40.2 years) received PUR1900 20 mg (n=18), 40 mg (n=16), or placebo (n=9). Baseline pre-dose FEV1% was 63.5±10.2 predicted; serum total IgE was 4469±55 kU/L. At week 16, PUR1900 40 mg significantly improved FEV1, reduced IgE, and achieved clinically meaningful improvement in ACQ-7. AQLQ improvement was not statistically significant. The frequency and severity of AEs were comparable across groups.

The abstract concluded that PUR1900 (40 mg) significantly improved lung function, asthma control, and IgE levels in adults with ABPA, with a favorable safety profile.

Should Cipla successfully market PUR1900 outside the United States, Pulmatrix will receive 2% royalties on any potential future net sales by Cipla outside the United States. Within the United States, we and Cipla will seek to monetize PUR1900 for indications where an orally inhaled antifungal may provide a therapeutic benefit or fulfill an unmet medical need.

Financial Overview

Research and Development Expenses

We expense research and development costs to operations as incurred. Research and development activities have been central to our business model. We have utilized a combination of internal and external efforts to advance product development from early-stage work to clinical trial manufacturing and clinical trial support. External efforts have included work with consultants and substantial work at contract research and manufacturing organizations. We have historically supported an internal research and development team and facility for our pipeline and other potential development programs, however following the closing of the transaction with MannKind Corporation (“MannKind” and such transactions, the “MannKind Transaction”) in the ~~third~~ ~~quarter~~year ofended December 31, 2024, the majority of our research and development employees were terminated, then hired by MannKind and our facility lease was assigned to MannKind. Going forward, we expect to utilize external resources for further development. Additionally, a Master Services Agreement between the Company and MannKind calls for MannKind to provide certain development services to the Company, including but not limited to, activities to develop dry powder formulations using iSPERSE™. Therefore, this agreement gives us access to our former development team.

To continue development of existing programs or opportunities identified for iSPERSE™ in any new indications, we will need to secure additional funding and anticipate additional development costs would be incurred. Because of the numerous risks and uncertainties associated with product development, however, we cannot determine with certainty the duration and completion costs of these or other current or future preclinical studies and clinical trials. The duration, costs and timing of our future clinical trials and development of our product candidates will depend on a variety of factors, including the selected development path and uncertainties associated with clinical and preclinical studies, clinical trial enrollment rates and changing government ~~regulation~~regulations. In addition, the probability of success for each product candidate will depend on numerous factors, including competition, manufacturing capability and commercial viability.

General and Administrative Expenses

General and administrative expenses consist principally of salaries, benefits and related costs such as stock-based compensation for personnel and consultants in executive, finance, business development, corporate communications and human resource functions, facility costs not otherwise included in research and development expenses, patent filing fees and legal fees. Other general and administrative expenses include travel expenses, expenses related to being a publicly traded company, professional fees for consulting, auditing and tax services, and expenses related to the Company’s exploration of strategic alternatives, including the Merger.

Critical Accounting Estimates

This management’s discussion and analysis of our financial condition and results of operations is based on our condensed consolidated financial statements, which have been prepared in accordance with U.S. GAAP. The preparation of these condensed consolidated financial statements requires us to make estimates and judgments that affect the reported amounts of assets, liabilities, revenues and expenses and the disclosure of contingent assets and liabilities in our condensed consolidated financial statements. We base our estimates on historical experience, known trends and events, and other assumptions that we believe are reasonable under the circumstances, and we evaluate these estimates on an ongoing basis. Actual results may differ from these estimates under different assumptions or conditions.

Critical Accounting Estimates

Our management’s discussion and analysis of our financial condition and results of operations is based on our condensed consolidated financial statements, which have been prepared in accordance with U.S. GAAP. The preparation of these condensed consolidated financial statements requires us to make estimates and judgments that affect the reported amounts of assets, liabilities, revenues and expenses and the disclosure of contingent assets and liabilities in our condensed consolidated financial statements. We base our estimates on historical experience, known trends and events, and other assumptions that we believe are reasonable under the circumstances, and we evaluate these estimates on an ongoing basis. Actual results may differ from these estimates under different assumptions or conditions.

As noted in the Annual Report, we have no critical accounting estimates that currently involve a significant level of uncertainty at the time the estimate was made, nor estimates for which changes in them have had or are reasonably likely to have a material effect on our financial condition or results of operations.

Results of Operations

Comparison of the Three Months Ended ~~September~~March 3031, ~~2025,~~2026 and ~~2024~~2025

The following table sets forth our results of operations for each of the periods set forth below (in thousands):

	Three Months Ended September 30,
	Three Months Ended March 31,
	2025			2024			Change
	2026			2025			Change
Revenues	$	-			366			(366	)
Operating expenses:
Research and development	$	83		$	~~814~~19		$	(~~806~~16	)
General and administrative		~~858~~1,289			21,~~209~~828			(~~1,351~~539	)
Total operating expenses		~~866~~1,292			31,~~023~~847			(~~2,157~~555	)
Loss from operations		(~~866~~1,292	)		(21,~~657~~847	)		~~1,791~~555
Other income (expense):
Interest income		3012			~~101~~53			(7141	)
Other expense, net		(41	)		(31	)		(10	)
Fair value adjustment of warrants		-			66			(66	)
Net loss	$	(877	)		(2,587	)		1,710
Other income (expense), net		108			(80	)		188
Net loss	$	(1,172	)	$	(1,808	)	$	636

~~Revenues~~Research —and Nodevelopment ~~revenues~~expenses ~~were~~— ~~recognized~~Research ~~for~~and ~~the~~development ~~three~~expenses ~~months~~were ~~ended~~less ~~September~~than ~~30, 2025, as compared to~~ $0.41 million for both the three months ended March ~~September 30~~31, ~~2024~~2026, aand ~~decrease of $0~~2025.4 ~~million.~~All ~~The~~clinical ~~decrease~~development is ~~primarily~~currently ~~related~~on tohold ~~completion~~while ofwe ~~the~~work ~~wind~~to ~~down~~license ofor ~~the PUR1900~~monetize ~~Phase~~our 2b clinical ~~trial during the year ended December 31, 2024~~assets.

~~Research~~General and ~~development~~administrative expenses — ~~Research~~General and ~~development~~administrative expenses were ~~less than~~ $0.1.3 million for the three months ended ~~September~~March 31, 302026, ~~2025,~~ as compared to $01.8 million for the three months ended ~~September~~March 3031, ~~2024~~2025, a decrease of approximately $0.85 million. The decrease ~~was~~ was primarily due to ~~$0.6~~higher ~~million~~costs ~~less~~incurred ~~employment~~in ~~and other operating cost following~~ the ~~MannKind~~three ~~Transaction~~months ~~and~~ended ~~$0.2~~March ~~million~~31, ~~less cost incurred on the PUR1900 program~~2025, ~~for~~related ~~which~~to the ~~winding~~preparation ~~down~~and filing of ~~the~~a ~~Phase~~registration statement 2band ~~clinical~~amendments ~~trial~~thereto ~~was~~on ~~completed~~Form ~~during~~S-4 with the ~~year ended December 31, 2024~~SEC.

General and administrative expenses — General and administrative expenses were $0.9 million for the three months ended September 30, 2025, as compared to $2.2 million for the three months ended September 30, 2024, a decrease of approximately $1.4 million. The decrease was primarily due to decreased employment, legal and professional services costs.

Comparison of the Nine Months Ended September 30, 2025, and 2024

The following table sets forth our results of operations for each of the periods set forth below (in thousands):

	Nine Months Ended September 30,
	2025			2024			Change
Revenues	$	-			7,803			(7,803	)
Operating expenses:
Research and development		41			7,160			(7,119	)
General and administrative		4,220			5,836			(1,616	)
Loss on MannKind Transaction		-			2,618			(2,618	)
Total operating expenses		4,261			15,614			(11,353	)
Loss from operations		(4,261	)		(7,811	)		3,550
Other income (expense):
Interest income		124			394			(270	)
Fair value adjustment of warrants		67			-			67
Other expense, net		(164	)		(156	)		(8	)
Net loss	$	(4,234	)		(7,573	)		3,339

Revenues — No revenues were recognized for the nine months ended September 30, 2025, as compared to $7.8 million for the nine months ended September 30, 2024, a decrease of $7.8 million. The decrease is primarily related to completion of the wind down of the PUR1900 Phase 2b clinical trial during the year ended December 31, 2024.

Research and development expenses — Research and development expenses were less than $0.1 million for the nine months ended September 30, 2025, as compared to $7.2 million for the nine months ended September 30, 2024, a decrease of approximately $7.1 million. The decrease was primarily due to $5.0 million less employment and other operating cost following the MannKind Transaction and $2.1 million less cost incurred on the PUR1900 program, for which the winding down of the Phase 2b clinical trial was completed during the year ended December 31, 2024.

General and administrative expenses — General and administrative expenses were $4.2 million for the nine months ended September 30, 2025, as compared to $5.8 million for the nine months ended September 30, 2024, a decrease of approximately $1.6 million. The decrease was primarily due to $2.8 million of decreased employment and other operating costs, partially offset by $1.2 million of costs related to the Merger.

Liquidity and Capital Resources

~~Through~~Sources ~~September 30, 2025, we incurred an accumulated deficit~~ of $301.4 million, primarily as a result of expenses incurred through a combination of research and development activities related to our various product candidates and general and administrative expenses supporting those activities. We have financed our operations since inception primarily through the sale of preferred and common stock, the issuance of convertible promissory notes, term loans, and collaboration and license agreements. Our total cash and cash equivalents balance as of September 30, 2025, was $4.8 million.Liquidity

WeThrough ~~anticipate~~March ~~that~~31, 2026, we ~~will~~incurred ~~continue~~an toaccumulated ~~incur~~deficit ~~significant~~of ~~expenses~~$303.5 ~~in connection with pursuing strategic alternatives~~million, ~~including~~primarily as ~~related to~~a ~~and~~result inof ~~connection~~expenses ~~with~~incurred ~~the~~through ~~Merger.~~a ~~Contingent~~combination of onresearch ~~securing additional funding~~ and ~~continuing~~ development ofactivities ~~our~~related ~~program candidates, we anticipate that we would continue~~ to ~~incur~~our ~~losses~~various ~~over~~product ~~the~~candidates ~~next~~and ~~several~~general ~~years~~and ~~due~~administrative toexpenses ~~development~~supporting ~~costs~~those activities. ~~associated~~We ~~with~~have financed our ~~iSPERSE™ pipeline~~operations ~~programs.~~since Weinception ~~expect~~primarily ~~that~~through wethe ~~would~~sale ~~need~~of ~~additional~~preferred ~~capital~~and tocommon ~~fund~~stock, ~~our~~the ~~operations~~issuance asof convertible wepromissory ~~continue~~notes, toterm ~~incur~~loans, ~~research~~ and ~~development and~~collaboration ~~general~~ and ~~administrative~~license ~~expenses~~agreements. WeOur ~~may~~total ~~raise~~cash ~~such~~and ~~capital~~cash ~~through~~equivalents abalance ~~combination~~as of March ~~equity offerings~~31, ~~debt financings~~2026, ~~other third-party~~was ~~funding~~$3.3 ~~and~~million ~~other~~plus ~~collaborations~~$0.7 ~~and~~million ~~strategic~~in ~~alliances~~restricted cash.

We expect that our existing cash and cash equivalents as of September 30, 2025, will enable us to fund our corporate operating expenses for at least the next 12 months following the date of this Quarterly Report on Form 10-Q. We have based our projections of operating capital requirements on assumptions that may prove to be incorrect, and we may use all of our available capital resources sooner than we expect. Because of the numerous risks and uncertainties associated with the Merger, research, development, achievement of contingent milestones and commercialization of pharmaceutical products, we are unable to estimate the exact amount of our operating capital requirements.20

Going Concern

The accompanying unaudited financial statements have been prepared assuming that we will continue as a going concern within one year after the date that the financial statements are issued. Our future operations are highly dependent on the success of the Merger and there can be no assurances that the Merger will be successfully consummated. If the Merger is not consummated, we may seek other strategic alternatives or pursue a dissolution and liquidation.

As of March 31, 2026, we had $3.3 million in cash and cash equivalents, as well as $0.7 million in restricted cash that would become unrestricted following consummation of the Merger or upon any termination of the Merger Agreement in accordance with its terms. We expect to incur significant costs in connection with the Merger and even if the Merger is ultimately not consummated, including legal and professional services costs related to filing registration statements with the SEC and obtaining shareholder approval.

In order to continue development of our programs, we would need to secure substantial additional funding in the future, from one or more equity or debt financings, collaborations, or other sources. Additional funding may not be available to us on acceptable terms, or at all. Contingent on securing additional funding and continuing development of our program candidates, we anticipate that we would continue to incur losses over the next several years due to development costs associated with our iSPERSE™ pipeline programs.

Cash Flows

We have no material off-balance sheet arrangements that have or are reasonably likely to have a current or future effect on our financial condition, changes in financial condition, revenues or expenses, results of operations, liquidity, capital expenditures or capital resources that is material to investors.

The following table sets forth the major sources and uses of cash for each of the periods set forth below (in thousands):

	Nine Months Ended September 30,
	Three Months Ended March 31,
	2025			2024
	2026			2025
Net cash used in operating activities	$	(41,~~727~~067	)	$	(91,~~455~~813	)
Net cash used in investing activities		-			(398	)
Net cash provided by financing activities		1,000			-
Net decrease in cash, cash equivalents, and restricted cash	$	(~~4,727~~67	)	$	(91,~~853~~813	)

Net cash used in operating activities

Net cash used in operating activities for the ~~nine~~three months ended ~~September~~March 3031, ~~2025~~2026, was $41.71 million, which was primarily the result of $41.2 million of net loss, partially offset by $0.41 million of cash ~~outflows~~flows associated with changes in operating assets and liabilities ~~and less than $0~~.~~1 million in net non-cash adjustments.~~

Net cash used in operating activities for the ~~nine~~three months ended ~~September~~March 3031, ~~2024~~2025, was $91.58 million, which was primarily the result of $71.68 million of net loss and $50.41 million in net non-cash adjustments, partially offset by $0.1 million of cash outflows associated with changes in operating assets and liabilities~~, partially offset by $3~~.~~6 million of net non-cash adjustments.~~

Net cash used in investing activities

No net cash was used in investing activities for the ~~nine~~three months ended ~~September~~March 3031, ~~2025~~2026. ~~Net cash used in investing activities for the nine months ended September 30, 2024, was $0.4 million, which was due to purchases of property and equipment.~~

Net cash provided by financing activities

Net cash provided by financing activities was $1.0 million for the three months ended March 31, 2026, resulting from the sale of Series B Convertible Preferred Stock during the period. Issuance costs attributable to this sale have not yet been paid.

Financings

2026 Series B Convertible Preferred Stock Private Placement

In connection with the entry into the Merger Agreement, we entered into a Securities Purchase Agreement, dated as of March 26, 2026, with an affiliate of Eos (the “Buyer”), pursuant to which we agreed to issue and sell to the Buyer in a private placement an aggregate of 1,000 shares of Series B Convertible Preferred Stock for aggregate gross proceeds of $1.0 million, which we received during the three months ended March 31, 2026. The Company delivered the shares of Series B Convertible Preferred Stock to the Buyer on April 16, 2026.

At The Market Offering Agreement

In May 2021, we entered into the At The Market Offering Agreement (the “Sales Agreement”) with H.C. Wainwright (“HCW”) to act as our sales agent with respect to the issuance and sale of up to $20,000,000 of our shares of common stock, from time to time in an “at-the-market” offering (the “ATM Offering”). Upon filing of the Annual Report, we continued to be subject to General Instruction I.B.6 of Form S-3, pursuant to which in no event will we sell our common stock in a registered primary offering using Form S-3 with a value exceeding more than one-third of our public float in any 12 calendar month period so long as our public float remains below $75,000,000. Therefore, the amount we may be able to raise using the ATM Offering will be significantly less than $20,000,000, until such time as our public float held by non-affiliates exceeds $75,000,000.

Sales of common stock under the Sales Agreement are made pursuant to an effective shelf registration statement on Form S-3, which was filed with the SEC on May 17, 2024, and subsequently declared effective on May 30, 2024 (File No. 333-279491), and a related prospectus. HCW acts as our sales agent on a commercially reasonable efforts basis, consistent with its normal trading and sales practices and applicable state and federal laws, rules and regulations and the rules of Nasdaq. If expressly authorized by us, HCW may also sell our common stock in privately negotiated transactions. There is no specific date on which the ATM Offering will end, there are no minimum sale requirements and there are no arrangements to place any of the proceeds of the ATM Offering in an escrow, trust or similar account. HCW is entitled to compensation at a fixed commission rate of 3.0% of the gross proceeds from the sale of our common stock pursuant to the Sales Agreement.

During the ~~nine~~three months ended ~~September~~March 3031, ~~2025~~2026, and ~~2024~~2025, no shares of our common stock were sold under the Sales Agreement.

Known Trends, Events and Uncertainties

The Company is subject to risks and uncertainties including, should it resume development of its product candidates, risks and uncertainties common to companies in the biopharmaceutical industry, including but not limited to, risks associated with completing preclinical studies and clinical trials, receiving regulatory approvals for product candidates, development by competitors of new biopharmaceutical products, dependence on key personnel, protection of proprietary technology, compliance with government regulations and the ability to secure additional capital to fund operations. Should the Company resume development of its product candidates, significant additional research and development efforts, including preclinical and clinical testing and regulatory approval, prior to commercialization, would be required. These efforts would require significant amounts of additional capital, adequate personnel and infrastructure and extensive compliance-reporting capabilities. Even if the Company’s product development efforts are successful, should the Company resume development of its product candidates, it is uncertain when, if ever, the Company would realize revenue from product sales. Ongoing conflicts, such as in Venezuela, between Russia and Ukraine and in the Middle East may adversely affect the economy and political conditions in the United States may be adversely affected, and in turn, affect our business and financial condition. Additionally, recent changes to U.S. policy implemented by the U.S. Congress, the Trump administration or any new administration have impacted and may in the future impact, among other things, the U.S. and global economy, tariffs, international trade relations, unemployment, immigration, healthcare, taxation, the U.S. regulatory environment, inflation and other areas. Although we cannot predict the impact, if any, of these changes to our business, they could adversely ~~affect~~ affect our business.

Item 3. Quantitative and Qualitative Disclosures About Market Risk.

Not applicable.

Item 4. Controls and Procedures.

Disclosure Controls and Procedures

Our Principal Executive Officer and Principal Financial Officer, after evaluating the effectiveness of our disclosure controls and procedures (as defined in Rules 13a-15(e) and 15d-15(e) promulgated under the Securities Exchange Act of 1934, as amended (the “Exchange Act”)) as of the end of the period covered by this Quarterly Report on Form 10-Q, have concluded that, based on such evaluation, our disclosure controls and procedures were effective to ensure that information required to be disclosed by us in the reports that we file or submit under the Exchange Act is recorded, processed, summarized and reported, within the time periods specified in the SEC’s rules and forms, and is accumulated and communicated to our management, including our Principal Executive Officer and Principal Financial Officer as appropriate to allow timely decisions regarding required disclosure.

In designing and evaluating our disclosure controls and procedures, our management recognizes that any controls and procedures, no matter how well designed and operated, can provide only reasonable assurance of achieving the desired control objectives, and our management necessarily is required to apply its judgment in evaluating the cost-benefit relationship of possible controls and procedures.

Changes in Internal Controls over Financial Reporting

There were no changes in our internal control over financial reporting that occurred during the quarter ended ~~September~~March 3031, ~~2025,~~2026 that have ~~materially~~ materially affected, or are reasonably likely to materially affect, our internal control over financial reporting.

PART II—OTHER INFORMATION

Item 1. Legal Proceedings.

From time to time, we may be involved in litigation that arises through the normal course of business. As of the date of this filing, we are not aware of any material legal proceedings to which we or any of our subsidiaries is a party or to which any of our property is subject, nor are we aware of any such threatened or pending litigation or any such proceedings known to be contemplated by governmental authorities.

We are not aware of any material proceedings in which any of our directors, officers, or affiliates or any registered or beneficial stockholder of more than 5% of our common stock, or any associate of any of the foregoing, is a party adverse to or has a material interest adverse to, us or any of our subsidiaries.

Item 1A. Risk Factors.

Investing in our common stock involves a high degree of risk. You should carefully consider the risks and uncertainties described in Part I, Item 1A under the heading “Risk Factors” in our Annual Report on Form 10-K for the year ended December 31, ~~2024~~2025, in addition to the risk factors below other information included in this Quarterly Report on Form 10-Q before making an investment decision regarding our common stock. If any of these risks actually occur, our business, financial condition, or operating results would likely suffer, possibly materially, the trading price of our common stock could decline, and you could lose part or all of your investment.

Risks Related to our Financial Condition

We have a history of recurring losses and our unaudited condensed consolidated financial statements have been prepared on a going concern basis, and do not include adjustments that might be necessary if we are unable to continue as a going concern. If we are unable to raise capital when needed, we could be forced to delay, reduce or eliminate any product development programs or commercialization efforts.

Our unaudited condensed consolidated financial statements have been prepared on a going concern basis, which contemplates the realization of assets and the satisfaction of liabilities in the normal course of business. As of March 31, 2026, our cash and cash equivalents balance was approximately $3.3 million, with an additional $0.7 million in restricted cash.

The Company’s future operations are highly dependent on the success of the Merger and there can be no assurances that the Merger will be successfully consummated. If the Merger is not consummated, the Company may seek other strategic alternatives or pursue a dissolution and liquidation.

We anticipate that our cash position is sufficient to fund our operations at least through the anticipated closing of the proposed Merger with Eos. However, management believes that without the closing of the Merger, given our current cash position and forecasted negative cash flows from operating activities over the next twelve months, there is substantial doubt about our ability to continue as a going concern after the date that is one year from the date that these financial statements are issued. The consolidated financial statements do not include any adjustments relating to the recoverability and classification of asset amounts or the classification of liabilities that might be necessary should we be unable to continue as a going concern.

We will need to raise additional capital to finance our losses and negative cash flows from operations and may continue to be dependent on additional capital raising as long as our products do not reach commercial profitability. There are no assurances that we would be able to raise additional capital on terms favorable to it. If we are unsuccessful in commercializing our products and raising capital, we will need to reduce activities, curtail, or cease operations. Even if we succeed in commercializing our new products, we may not be able to generate sufficient revenues to cover our expenses and achieve profitability or be able to maintain profitability.

General Risk Factors

Global economic and political instability and conflicts, such as the conflicts in Venezuela, between Russia and Ukraine or in the Middle East, could adversely affect our business, financial condition or results of operations.

Our business could be adversely affected by unstable economic and political conditions within the United States and foreign jurisdictions and geopolitical conflicts, such as the conflicts in Venezuela, between Russia and Ukraine or in the Middle East. While we do not have any customer or direct supplier relationships in impacted areas at this time, the current military conflict, and related sanctions, as well as export controls or actions that may be initiated by nations including the United States, the European Union or Russia (e.g., potential cyberattacks, disruption of energy flows, etc.) and other potential uncertainties could adversely affect our business and/or our supply chain, business partners, employees or customers, and interrupt our ability to supply products, or otherwise adversely impact our business.

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

(a)

Unregistered Sales of Equity Securities

None.

(b)

Issuer Purchases of Equity Securities.

None.

Item 3. Defaults Upon Senior Securities.

None.

Item 4. Mine Safety Disclosures.

Not applicable.

Item 5. Other Information.

None.

Item 6. Exhibits.

See “Index to Exhibits” following the signature page to this Form 10-Q for a list of exhibits filed or furnished with this Quarterly Report on Form 10-Q.

2425

SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.

	PULMATRIX, INC.
Date: October 16, 2025	By:	/s/ Peter Ludlum
Date: May 15, 2026	By:	/s/ Peter Ludlum
		Peter Ludlum
		Interim Chief Executive Officer and Interim Chief Financial Officer
		(Principal Executive, Financial and Accounting Officer)

INDEX TO EXHIBITS

Exhibit Number		Exhibit Description
31.1*		Certification of the Principal Executive Officer and Principal Financial Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002
32.1**		Certification of Principal Executive Officer and Principal Financial Officer pursuant to Section 906 of the Sarbanes-Oxley Act of 2002
101. INS*		Inline XBRL Instance Document
101.SCH*		Inline XBRL Taxonomy Extension Schema Document
101.CAL*		Inline XBRL Taxonomy Extension Calculation Linkbase 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 (formatted as inline XBRL and contained in Exhibit 101)
*		Filed herewith.
**		Furnished herewith.

INDEX TO EXHIBITS

Exhibit Number		Exhibit Description

2.1***		Agreement and Plan of Merger and Reorganization, dated as of March 26, 2026, by and among Pulmatrix, Inc., PUOS Merger Sub, Inc., and Eos SENOLYTIX, Inc. (incorporated by reference to Exhibit 2.1 to the Company’s Current Report on Form 8-K filed with the SEC on March 26, 2026).

3.1		Certificate of Designation of Preferences, Rights and Limitations of Series B Convertible Preferred Stock, filed on March 26, 2026 (incorporated by reference to Exhibit 3.1 to the Company’s Current Report on Form 8-K filed with the SEC on March 26, 2026).

10.1		Form of Support Agreement (incorporated by reference to Exhibit 10.1 to the Company’s Current Report on Form 8-K filed with the SEC on March 26, 2026).

10.2		Form of Lock-Up Agreement (incorporated by reference to Exhibit 10.2 to the Company’s Current Report on Form 8-K filed with the SEC on March 26, 2026).

10.3		Form of Securities Purchase Agreement, dated as of March 26, 2026, by and between the Company and the investor named therein (incorporated by reference to Exhibit 10.3 to the Company’s Current Report on Form 8-K filed with the SEC on March 26, 2026).

10.4		Form of Voting Agreement, dated as of March 26, 2026, by and between the Company and the holder named therein (incorporated by reference to Exhibit 10.4 to the Company’s Current Report on Form 8-K filed with the SEC on March 26, 2026).

31.1*		Certification of the Principal Executive Officer and Principal Financial Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002

32.1**		Certification of Principal Executive Officer and Principal Financial Officer pursuant to Section 906 of the Sarbanes-Oxley Act of 2002

101. INS*		Inline XBRL Instance Document

101.SCH*		Inline XBRL Taxonomy Extension Schema Document

101.CAL*		Inline XBRL Taxonomy Extension Calculation Linkbase 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 (formatted as inline XBRL and contained in Exhibit 101)

*		Filed herewith.
**		Furnished herewith.
***		Exhibits and/or schedules have been omitted pursuant to Item 601(a)(5) of Regulation S-K. The registrant hereby undertakes to furnish supplementally copies of any of the omitted exhibits and schedules upon request by the SEC; provided, however, that the registrant may request confidential treatment pursuant to Rule 24b-2 under the Exchange Act for any exhibits or schedules so furnished.

Filing Compare · Pulmatrix, Inc.