FDA
approval
· 2017-08-01
FDA Approved: IDHIFA — Original Application (Celgene Corporation)
Summary
FDA approves IDHIFA (enasidenib) in the original application for adult patients with relapsed or refractory acute myeloid leukemia harboring an IDH2 mutation.
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Diseases / indications
Drugs mentioned
Snippet
ORIG AP for IDHIFA (ENASIDENIB MESYLATE)