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A Phase 1, Multicenter, Open-Label, Safety Study of AG-120 or AG-221 in Combination With Induction Therapy and Consolidation Therapy in Patients With Newly Diagnosed Acute Myeloid Leukemia With an IDH1 and/or IDH2 Mutation

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Study Phase

Phase 1

Therapeutic Area


IndicationAcute Myeloid Leukemia
SponsorInstitut de Recherches Internationales Servier
Active substance/
Medical device

AG-120, AG-221

Active Substance CodeAG-120, AG-221
Protocol CodeAG120-221-C-001
EudraCT Code2015-004290-33
NCT CodeNCT02632708

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