drugset / Trial / NCT03969420
Study of Alvocidib in Patients With Relapsed/Refractory AML Following Treatment With Venetoclax Combination Therapy
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Cytarabine | Small molecule | — | Subcutaneous |
| Subject | alvocidib | Small molecule | — | Intravenous |