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Nektar Announces UCB's Cimzia(R) Approved by U.S. FDA for Adult Patients Suffering From Moderate to Severe Rheumatoid Arthritis
Date:5/14/2009

nine approved partnered products in the U.S. or Europe today, including Roche's PEGASYS(R) for hepatitis C and Amgen's Neulasta(R) for neutropenia.

Nektar is headquartered in San Carlos, California, with additional R&D operations in Huntsville, Alabama and Hyderabad, India.

This press release contains forward-looking statements that reflect management's current views regarding the value and potential of the company's technology platform, and the company's collaborations with third parties. These forward-looking statements involve numerous risks and uncertainties, including (1) the commercial success of Cimzia(R) cannot be assured and the amount of our future manufacturing revenue from Cimzia(R) is uncertain, (2) any success with Cimzia(R) is not necessarily predictive of clinical or commercial success with any other PEGylated or advanced polymer conjugation products, and (3) other important risks and uncertainties set forth in the company's most recent Quarterly Report on Form 10-Q filed on May 8, 2009 and its Annual Report on Form 10-K filed with the Securities and Exchange Commission on March 6, 2009. Actual results could differ materially from the forward-looking statements contained in this press release. The company undertakes no obligation to update forward-looking statements, whether as a result of new information, future events or otherwise.

For more information on Nektar Therapeutics, please visit www.nektar.com.

    Contact:
    Jennifer Ruddock, 650-631-4954
    Nektar Therapeutics


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