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Cystic Fibrosis Trial In Children Returns Positive Data
Date:4/3/2008

ria Subjects with a known diagnosis of cystic

fibrosis, FEV1 < 70% of predicted, of either

gender, aged between 8 and 19 years of age and

currently receiving rhDNase or eligible to

receive rhDNase.

Primary End Points To compare and contrast the effect on FEV1 of:

1: Bronchitol to rhDNase

2: Bronchitol + rhDNase to rhDNase

Secondary End Points To assess whether:

1: the effects of Bronchitol are additive to

rhDNase

2: Bronchitol reduces the bacterial load in

the lung

3: the effects of Bronchitol are beneficial

to quality of life

Trial Location United Kingdom

Commercial partners Pharmaxis Ltd

Sponsor Investigator initiated, Pharmaxis supported

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 w
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SOURCE Pharmaxis Ltd
Copyright©2008 PR Newswire.
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