drugset / Trial / NCT04827719

BST-236 as a Single Agent in Adults With Relapsed or Refractory AML or HR-MDS

NCT04827719 ↗

Phase 2 Completed 38 enrolled Groupe Francophone des Myelodysplasies
NaSingle-groupOpen-labelTreatment

Summary

To assess the efficacy, and safety of BST-236 in patients unfit for intensive chemotherapy with AML or HR MDS that failed or relapsed following first line therapy

Timeline

Start
2021-05-01
Primary completion
2025-01-13
Completion
2025-01-13

Drugs

EvaluationDrugModalityDoseRoute
Subject aspacytarabine Small molecule 2.3 g Intravenous
Subject aspacytarabine Small molecule 4.5 g Intravenous