drugset / Trial / NCT02287233

A Study Evaluating Venetoclax in Combination With Low-Dose Cytarabine in Treatment-Naïve Participants With Acute Myelogenous Leukemia

NCT02287233 ↗

Phase 1/2 Completed 94 enrolled AbbVie Genentech, Inc. · collab
Non-randomizedSequentialOpen-labelTreatment

Summary

This study consists of two parts: A Phase 1 dose-escalation part that will evaluate the safety and pharmacokinetic profile of venetoclax in combination with low-dose cytarabine (LDAC), define the maximum tolerated dose (MTD), and generate data to support a recommended Phase 2 dose (RPTD) in treatment-naïve participants with acute myelogenous leukemia (AML); and a Phase 2 part that will evaluate if the RPTD has sufficient efficacy and acceptable toxicity to warrant further development of the combination therapy.

Timeline

Start
2014-12-31
Primary completion
2021-08-10
Completion
2021-08-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Venetoclax Small molecule 600 mg Oral
Subject Venetoclax Small molecule 800 mg Oral
Background Cytarabine Small molecule 20 mg/m2 Subcutaneous