drugset / Trial / NCT02265731

Study Evaluating Venetoclax in Subjects With Hematological Malignancies

NCT02265731 ↗

Phase 1/2 Completed 38 enrolled AbbVie Genentech, Inc. · collab
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This study is evaluating the safety, pharmacokinetic profile and efficacy of venetoclax under a once daily dosing schedule in Japanese participants with hematological malignancies.

Timeline

Start
2014-09-22
Primary completion
2021-03-12
Completion
2021-03-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Azacitadine Unknown 75 mg/m2 Intravenous
Subject Rituximab Monoclonal antibody 500 mg/m2 —
Subject Venetoclax Small molecule — —