drugset / Trial / NCT03173248

Study of AG-120 (Ivosidenib) vs. Placebo in Combination With Azacitidine in Participants With Previously Untreated Acute Myeloid Leukemia With an IDH1 Mutation

NCT03173248

Phase 3 Active not recruiting 146 enrolled Servier
RandomizedParallel-groupTriple-blindTreatment

Summary

Study AG120-C-009 is a global, Phase 3, multicenter, double-blind, randomized, placebo-controlled clinical trial to evaluate the efficacy and safety of AG-120 (ivosidenib) + azacitidine vs placebo + azacitidine in adult participants with previously untreated IDH1m AML who are considered appropriate candidates for non-intensive therapy. The primary endpoint is event-free survival (EFS). The key secondary efficacy endpoints are overall survival (OS), rate of complete remission (CR), rate of CR and complete remission with partial hematologic recovery (CRh), and overall response rate (ORR). Participants eligible for study treatment based on Screening assessments will be randomized 1:1 to receive oral AG-120 or matched placebo, both administered in combination with subcutaneous (SC) or intravenous (IV) azacitidine. An estimated 200 participants will take part in the study.

Timeline

Start
2017-06-26
Primary completion
2021-03-18
Completion
2026-06-30

Drugs

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