drugset / Trial / NCT02677922

A Study to Assess the Safety and Efficacy of Two Combinations of Isocitrate Dehydrogenase (IDH) Mutant Targeted Therapies Plus Azacitidine in Participants With Newly Diagnosed Acute Myeloid Leukemia (AML) Harboring IDH Mutations Who Are Not Candidates to Receive Intensive Induction Chemotherapy

NCT02677922

Phase 1/2 Active not recruiting 130 enrolled Celgene Corporation
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study are 1. to determine the recommended combination dose of AG-120 and AG-221 separately when administered with azacitidine and, 2. to investigate the safety, tolerability, and efficacy of the combinations of AG-120 with azacitidine and AG-221 with azacitidine versus with azacitidine alone in participants with acute myeloid leukemia (AML) with the isocitrate dehydrogenase (IDH) enzyme isoforms 1 or 2 mutations, respectively.

Timeline

Start
2016-06-03
Primary completion
2018-08-02
Completion
2026-09-30

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Enasidenib Small molecule 100 mg Oral
Subject Enasidenib Small molecule 200 mg Oral
Subject Ivosidenib Small molecule 500 mg Oral
Background Azacitidine Other / unclassified 75 mg/m2 Subcutaneous