drugset / Trial / NCT02632708

Safety Study of AG-120 or AG-221 in Combination With Induction and Consolidation Therapy in Participants With Newly Diagnosed Acute Myeloid Leukemia (AML) With an IDH1 and/or IDH2 Mutation

NCT02632708

Phase 1 Active not recruiting 153 enrolled Servier Celgene Corporation · collab
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this Phase I, multicenter, clinical trial is to evaluate the safety of AG-120 and AG-221 when given in combination with standard AML induction and consolidation therapy. The study plans to evaluate up to 2 dose levels of AG-120 in participants with an isocitrate dehydrogenase protein 1 (IDH1) mutation and up to 2 dose levels of AG-221 in participants with an isocitrate dehydrogenase protein 2 (IDH2) mutation. AG-120 or AG-221 will be administered with 2 types of AML induction therapies (cytarabine with either daunorubicin or idarubicin) and 2 types of AML consolidation therapies (mitoxantrone with etoposide \[ME\] or cytarabine). After consolidation therapy, participants may continue on to maintenance therapy and receive daily treatment with single-agent AG-120 or AG-221 until relapse, development of an unacceptable toxicity, or hematopoietic stem cell transplant (HSCT). The study will end when all participants have discontinued study treatment.

Timeline

Start
2015-12-31
Primary completion
2018-12-13
Completion
2026-07-24

Drugs

EvaluationDrugModalityDoseRoute
Subject Daunorubicin Small molecule
Subject Enasidenib Small molecule 100 mg Oral
Subject Idarubicin Small molecule
Subject Ivosidenib Small molecule 500 mg Oral
Background Cytarabine Small molecule
Background Etoposide Small molecule
Background Mitoxantrone Small molecule