CONFORMED COPY

SECURITIES AND EXCHANGE COMMISSION

Washington D.C. 20549

FORM 6-K

REPORT OF FOREIGN PRIVATE ISSUER
Pursuant to Rule 13a-16 or 15d-16 of
the Securities Exchange Act of 1933

May 414, 2009

Pharmaxis Ltd

2/10 Rodborough Road,
Frenchs Forest, NSW 2086
Australia

(Indicate by check mark whether the registrant files or will file annual reports under cover of Form 20-F or Form 40-F.)

Form 20-F þ Form 40-F o

(Indicate by check mark whether the registrant by furnishing the information contained in this form is also thereby furnishing the information to the Commission pursuant to Rule 12g3-2(b) under the Securities Exchange Act of 1934.)

Yes o No þ

(If “Yes” is marked, indicate below the file number assigned to the registrant in connection with Rule 12g3-2(b): 82- .)

ASX/NASDAQ Media Release 0414 May 2009

~~Pharmaxis~~U.S. ~~Announces~~FDA ~~Positive~~Accepts ~~Results~~AridolTM ofNew ~~Phase~~Drug 3Application ~~Cystic~~for ~~Fibrosis~~Review ~~Trial~~

~~Pharmaceutical company~~ Pharmaxis (ASX:PXS, ~~Nasdaq~~NASDAQ:PXSL) istoday ~~pleased~~announced toit ~~announce~~had ~~positive~~received ~~results~~notification offrom the United ~~its~~States ~~recently~~Food ~~completed~~and ~~international~~Drug ~~Phase~~Administration ~~III~~(FDA) that ~~trial~~the ofNew ~~BronchitolTM~~Drug inApplication ~~people~~(NDA) for ~~with~~its mannitol ~~cystic~~bronchial ~~fibrosis~~challenge test Aridol™ has been accepted for standard review. The ~~study~~FDA ~~represents~~will ~~one~~advise the result of the ~~largest~~review ~~clinical~~on ~~trials~~27 ~~conducted in cystic fibrosis~~December 2009.

~~The~~Pharmaxis ~~primary~~is ~~endpoint~~seeking ofapproval ~~the~~for ~~trial~~Aridol ~~was~~for to“the ~~assess~~assessment ~~whether~~of ~~Bronchitol~~bronchial ~~improves~~hyperresponsiveness ~~lung function as~~to ~~measured~~aid ~~by a change~~ in ~~Forced~~the ~~Expiratory~~diagnosis ~~Volume~~of inpatients 1with ~~second~~symptoms ~~(FEV1)~~of ~~when~~or ~~administered 400~~suggestive mgof ~~twice per day for six months~~asthma.” ~~The~~Asthma ~~clinical~~affects ~~trial~~more than ~~comfortably~~34 million ~~met~~people ~~this~~in ~~endpoint~~the U.S. ~~Patients treated~~ with ~~Bronchitol~~an ~~had~~annual aeconomic ~~statistically~~cost ~~significant improvement in lung function from baseline~~ of 6$19.~~6% (p=0~~7 billion.~~001~~ ~~versus~~When ~~placebo).~~approved, Aridol ~~Lung~~will ~~function~~be ~~improved~~the atfirst ~~week~~dry 6powder ~~and~~bronchial ~~was~~challenge ~~sustained~~test ~~through~~available ~~to week~~in 26the U.S.

~~The~~Alan ~~key~~Robertson, ~~secondary~~Pharmaxis ~~endpoint~~Chief ofExecutive ~~the~~Officer ~~trial~~said: ~~was~~“We tohave ~~assess~~been ~~whether~~greatly ~~Bronchitol~~encouraged ~~further~~by ~~improves lung~~the ~~function~~interest inrespiratory ~~patients~~physicians ~~already~~have ~~being~~shown ~~treated~~in ~~with~~Aridol ~~the~~at ~~most~~recent ~~commonly~~U.S. ~~used~~scientific CFconferences. ~~therapeutic~~We estimate that 200,000 ~~dornase~~bronchial ~~alfa (PulmozymeTM).~~hyper-responsiveness ~~This~~tests ~~endpoint~~are ~~was~~performed ~~also~~in ~~successfully~~the ~~achieved.~~US ~~For~~each ~~patients~~year ~~being~~and ~~treated~~hope ~~with~~that ~~concurrent~~the ~~dornase~~introduction ~~alfa,~~of ~~FEV1~~a ~~improved~~dry ~~after~~powder ~~6 months~~test bykit ~~5.2%~~will ~~from~~encourage ~~baseline~~more physicians to utilize this ~~(p=0~~test when diagnosing asthma.~~002~~ ~~versus~~We ~~placebo)~~look forward to working with the FDA to complete the review.”

~~Over~~Aridol ~~the~~is ~~6 month~~approved ~~treatment~~for ~~period,~~sale ~~there~~in ~~was~~most ~~significant~~major ~~lung~~European ~~function~~countries, ~~improvement~~Australia ~~for~~and ~~both~~Korea. ~~those~~Aridol has been ~~patients~~included ~~being~~in ~~treated~~the ~~with~~Global ~~Bronchitol~~Initiative for Asthma guidelines, and ~~dornase~~in ~~alfa~~the ~~(p=0~~U.~~008~~S. ~~versus~~Asthma ~~placebo)~~Management Guidelines. It is one of the tests recommended by the World Anti-Doping Agency, and ~~those~~other ~~being~~sports ~~treated~~governing ~~with~~bodies ~~Bronchitol~~to ~~alone~~ensure ~~(p=0.015~~elite ~~versus~~athletes ~~placebo)~~who are asthmatic are properly diagnosed and treated.

Consistent loss of lung function, is the leading cause of death for people with cystic fibrosis and this deterioration now averages 1-2% per year.

Dr Alan Robertson, Pharmaxis Chief Executive Officer said: “We are delighted that Bronchitol performed so well in this important long term study and we now know that it can change the therapeutic landscape for many of the 75,000 people with this disease. In a trial which recruited a wide range of patients with varying disease severity, Bronchitol showed significant health benefits. As the first dry powder formulation to publish positive results in cystic fibrosis it promises convenience for patients who have complex daily schedules dominated by difficult treatment regimens.”

For the 324 subjects randomized, the treatment groups were balanced with respect to key demographic and background characteristics: the average age was approximately 23 years old, the mean lung function on entry to the trial was 62% of the predicted normal FEV1, and 55% of the population were using dornase alfa. The ages ranged from 6 years to 56 years and the lung function ranges were from 26% to 94% of the predicted FEV1.

In the trial subjects, Bronchitol was well-tolerated overall and had a favourable safety profile. At screening, only 7% of recruited subjects were unable to tolerate Bronchitol and were therefore not entered into the study. There was no difference in adverse events or serious adverse events between the treatment groups. The most common adverse event was cough, which was mild to moderate in most cases and similar between the treatment arms.

Page 1 of 3

The trial was conducted in 40 centres in the United Kingdom, Ireland, Australia and New Zealand. It was a double blind, placebo controlled study designed in consultation with the European Medicines Agency (EMEA) with the objective of seeking a marketing authorisation for Bronchitol for treating cystic fibrosis in Europe and elsewhere. Pharmaxis will now move to file a marketing application later this year.

The first scientific presentation of the results will be made at the June European Cystic Fibrosis Society meeting in France. In addition a more detailed account of the results of the trial is planned to be presented at the North American Cystic Fibrosis conference in Minneapolis in October.

Bronchitol has received Orphan Drug Designation and development fast track status from the U.S. Food and Drug Administration and Orphan Drug Designation from the European Medicines Agency.

Bronchitol is designed to hydrate the airway surface of the lungs, and promote normal lung mucus clearance. No new products have been approved anywhere in the world for cystic fibrosis for more than 10 years.

Dr Alan Robertson said: “We recognise that many people have been involved in the development of Bronchitol and their assistance has been invaluable. The trial was complex and challenging and this landmark result is a tribute to their efforts.”

#ENDS#

Dr Alan Robertson will host a teleconference to discuss the results on Tuesday 5th May at 8.00am (Sydney), (Monday 4th May at 6.00pm U.S. East Coast, 3.00pm U.S. West Coast).

Telephone access (toll free) details are below:

• Australia: 1800 131 617 • USA/Canada: 866 746 2596 • UK: 0800 376 8339 • NZ: 0800 446 958 • Switzerland: 0800 001 230

Online (global access): http://services.choruscall.com/links/pharmaxis090505.html

#ends#

SOURCE: Pharmaxis Ltd, Sydney, Australia
CONTACT: Alan Robertson — Chief Executive Officer
Ph: +61 2 9454 7200 or email alan.robertson@pharmaxis.com.au

RELEASED THROUGH:
Australia:
Felicity Moffatt, phone +61 418 677 701 or email felicity.moffatt@pharmaxis.com.au

United States:
Brandon Lewis, Trout Group, phone +1 646 378 2915 or email blewis@troutgroup.com

Page 2 of 3

Forward-Looking Statements
The statements contained in this media release that are not purely historical are forward-looking statements within the meaning of Section 21E of the Securities Exchange Act of 1934, as amended. Forward-looking statements in this media release include statements regarding our expectations, beliefs, hopes, goals, intentions, initiatives or strategies, including statements regarding the potential for Aridol and/or Bronchitol. All forward-looking statements included in this media release are based upon information available to us as of the date hereof, and we assume no obligation to update any such forward-looking statement as a result of new information, future events or otherwise. We can not guarantee that any product candidate will receive FDA or other regulatory approval or that we will seek any such approval. Factors that could cause or contribute to such differences include, but are not limited to, factors discussed in the “Risk Factors and Other Uncertainties” section of our Form 20-F lodged with the U.S. Securities and Exchange Commission.

Page 3 of 3

SIGNATURE

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.

	Pharmaxis Ltd (Registrant)
Date: May 4, 2009	By:	/s/ David McGarvey
Date: May 14, 2009	By:	/s/ David McGarvey
		Name:	David McGarvey
		Title:	Chief Financial Officer

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