drugset / Trial / NCT03969420

Study of Alvocidib in Patients With Relapsed/Refractory AML Following Treatment With Venetoclax Combination Therapy

NCT03969420 ↗

Phase 2 Terminated 11 enrolled Sumitomo Pharma America, Inc.
RandomizedParallel-groupOpen-labelTreatment

Summary

This study will evaluate the safety and efficacy of alvocidib in patients with AML who have either relapsed from or are refractory to venetoclax in combination with azacytidine or decitabine.

Timeline

Start
2020-01-15
Primary completion
2021-04-22
Completion
2021-05-14

Outcome

Outcome not reported

Stopped (Business): “Business decision to terminate the development of alvocidib program on 17 November 2020. Patients permitted on treatment until April 22, 2021. The last end-of-treatment follow-up completed on May 14, 2021.”

Drugs

EvaluationDrugModalityDoseRoute
Subject Cytarabine Small molecule — Subcutaneous
Subject alvocidib Small molecule — Intravenous