drugset / Trial / NCT03441555

A Study of Venetoclax and Alvocidib in Patients With Relapsed/Refractory Acute Myeloid Leukemia

NCT03441555

Phase 1 Completed 36 enrolled AbbVie Sumitomo Pharma America, Inc. · collab
NaSingle-groupOpen-labelTreatment

Summary

An open-label, dose-escalation study to assess the safety and pharmacokinetics (PK), to determine the dose limiting toxicity (DLT) and the recommended Phase 2 dose (RPTD), and to assess the preliminary efficacy of alvocidib with venetoclax when co-administered in participants with relapsed or refractory (R/R) acute myeloid leukemia (AML).

Timeline

Start
2018-05-30
Primary completion
2021-01-25
Completion
2021-01-25

Drugs

EvaluationDrugModalityDoseRoute
Subject Venetoclax Small molecule Oral
Subject alvocidib Small molecule Intravenous