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ODAC Unanimously Recommends GSK’s Promacta For ITP

This article was originally published in The Pink Sheet Daily

Executive Summary

FDA, committee members struggle to find ways to discourage long-term use of the drug for the chronic condition.

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GSK’s Promacta And Amgen’s Nplate Face Off In ITP Market

GlaxoSmithKline/Ligand's Promacta (eltrombopag) received FDA approval Nov. 20 as a second-line treatment of thrombocytopenia in patients with the rare blood disorder chronic idiopathic thrombocytopenic purpura. The approval was widely anticipated, although it came five months after the drug's original PDUFA date

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