Expert panel recommends U.S. approval of GSK's Promacta

06/1/2008 | Google · Wall Street Journal, The

An FDA advisory panel unanimously recommended the approval of Promacta, GlaxoSmithKline's platelet drug for treating chronic immune thrombocytopenic purpura. The panel did not vote on whether the FDA should put off authorizing marketing for the treatment, which was co-developed with Ligand Pharmaceuticals, until it assesses findings from ongoing trials. The agency is expected to hand down its decision by June 19.

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Google · Wall Street Journal, The

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