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FDA panel to discuss Roche arthritis drug July 29

Thu Jun 5, 2008 4:33am EDT

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LONDON, June 5 (Reuters) - Roche Holding AG's (ROG.VX) experimental arthritis drug Actemra will be considered for approval by a U.S. Food and Drug Administration panel on July 29.

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The new drug, which Roche views as a potential blockbuster, will be discussed by the watchdog's Arthritis Advisory Committee, according to the agency's telephone information line. (Reporting by Ben Hirschler)



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