drugset / Trial / NCT02966782

A Study Evaluating Venetoclax Alone and in Combination With Azacitidine in Participants With Relapsed/Refractory Myelodysplastic Syndromes (MDS)

NCT02966782 ↗

Phase 1 Completed 70 enrolled AbbVie Celgene; Genentech, Inc. · collab
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This is a Phase 1b, open-label, multicenter study designed to evaluate the safety and pharmacokinetics of venetoclax as a single-agent and in combination with azacitidine in participants with relapsed/refractory Myelodysplastic Syndromes (MDS).

Timeline

Start
2017-03-07
Primary completion
2023-04-05
Completion
2023-04-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Azacitidine Other / unclassified 75 mg/m2 Subcutaneous
Subject Venetoclax Small molecule 100 mg Oral
Subject Venetoclax Small molecule 200 mg Oral
Subject Venetoclax Small molecule 400 mg Oral