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Current | 2007 | 2006 | 2005 | 2004 | 2003 | 2002 | 2001 | 2000 | 1999 | 1998 | 1997 Rigel Announces Initiation of Phase 1 Clinical Trial of R343 for Allergic Asthma by its Partner Pfizer SOUTH SAN FRANCISCO, Calif. - December 06, 2007 Rigel Pharmaceuticals, Inc. (Nasdaq: RIGL) today announced that its corporate partner, Pfizer (NYSE: PFE), has begun a Phase 1 clinical trial of an inhaled formulation of Rigel’s small molecule syk kinase inhibitor, R343, for the treatment of allergic asthma. R343 is the third product candidate in Rigel’s clinical portfolio. Under the terms of the companies’ 2005 collaboration agreement, Rigel will receive a $5 million milestone payment from Pfizer for the commencement of this study. Pfizer retains exclusive rights to R343 and is responsible for its clinical development. “Developing an inhaled drug product that may address an important pathway in the allergic response causing asthmatic airway obstruction and tissue damage gives new hope to millions of asthma sufferers,” stated Donald G. Payan, M.D., executive vice president and chief scientific officer of Rigel. “We are proud to have Pfizer lead the development of R343.” Syk Kinase Inhibition in Allergic Asthma R343 will be delivered via the inhaled route using a dry powder inhaler and will initially be tested in healthy volunteers to evaluate its safety, dosing and pharmacodynamics. R343 is not orally bio-available and is a different molecule from R788. R788 is an orally bio-available syk kinase inhibitor in development by Rigel for various autoimmune and hematological indications, and is not part of this collaboration. About Rigel (www.rigel.com) This press release contains "forward-looking" statements, including statements related to the clinical development of R343 and the potential efficacy of Rigel's product candidates. Any statements contained in this press release that are not statements of historical fact may be deemed to be forward-looking statements. Words such as “believes,” "may," "expects," "goal" and similar expressions are intended to identify these forward-looking statements. These forward-looking statements are based upon Rigel’s current expectations. Forward-looking statements involve risks and uncertainties. There are a number of important factors that could cause Rigel's results to differ materially from those indicated by these forward-looking statements, including risks associated with Rigel’s drug discovery and development efforts, potential problems that may arise in clinical testing, as well as other risks detailed from time to time in Rigel's SEC reports, including its Form 10-Q for the quarter ended September 30, 2007. Rigel expressly disclaims any obligation or undertaking to update or revise any forward-looking statements made herein. Contact: Raul Rodriguez Media Contact: Susan C. Rogers, Alchemy Consulting, Inc. |
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