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Agios Pharmaceuticals announces U.S. FDA grants fast track designation to AG-221 for treatment of patients with Acute Myelogenous Leukemia That Harbor an IDH2 Mutation

Wednesday, 13 Aug 2014 08:30am EDT 

Agios Pharmaceuticals Inc:Says U.S. Food and Drug Administration (FDA) has granted Fast Track designation to AG-221 for treatment of patients with acute myelogenous leukemia (AML) that harbor an isocitrate dehydrogenase-2 (IDH2) mutation.AG-221 is first-in-class, oral, selective, potent IDH2 mutant inhibitor being evaluated in Phase 1 clinical trial in patients with advanced hematologic malignancies.