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Baxter Initiates Phase I Clinical Trial Of Longer-acting Recombinant FVIII Treatment For Hemophilia A

This release includes forward-looking statements concerning a Phase I trial of the Company's investigational compound BAX 855, including with respect to expectations related to clinical outcomes. The statements are based on assumptions about many important factors, including the following, which could cause actual results to differ materially from those in the forward-looking statements: timely submission and approval of anticipated regulatory filings;  clinical results validating the use of BAX 855  to treat patients with severe hemophilia A; satisfaction of regulatory and other requirements; actions of regulatory bodies and other governmental authorities; and other risks identified in Baxter's most recent filing on Form 10-K and other SEC filings, all of which are available on the company's website. Baxter does not undertake to update its forward-looking statements.

  1. What is Hemophilia? World Federation of Hemophilia. Accessed on: 29 June 2011. Available at: http://www.wfh.org/2/1/1_1_1_What_Is_Hemophilia.htm
  2. Frequently Asked Questions About Hemophilia. World Federation of Hemophilia. Accessed on: 24 August 2011.  Available at: http://www.wfh.org/index.asp?lang=EN
  3. Hemophilia A. National Hemophilia Foundation. Accessed on: 29 June 2011. Available at http://www.hemophilia.org/NHFWeb/MainPgs/MainNHF.aspx?menuid=180&contentid=45&rptname=bleeding.

 

Media Contacts Deb Spak, (847) 948-2349 Brian Kyhos, (847) 948-4210



Investor Contacts Mary Kay Ladone, (847) 948-3371 Clare Trachtman, (847) 948-3085

SOURCE Nektar Therapeutics

Copyright 2011 PR Newswire. All rights reserved. This material may not be published, broadcast, rewritten or redistributed.
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