drugset / Trial / NCT02826642

A Dose Finding Study of IDH305 With Standard of Care in IDH1 Mutant Acute Myeloid Leukemia

NCT02826642 ↗

Phase 1 Withdrawn Novartis Pharmaceuticals
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety, tolerability and potential efficacy of IDH305 with standard treatments for newly diagnosed IDH1R132 mutant acute myeloid leukemia (AML).

Timeline

Start
2016-08-26
Primary completion
2016-11-29
Completion
2016-11-29

Drugs

EvaluationDrugModalityDoseRoute
Subject IDH305 Small molecule — —