drugset / Trial / NCT02544438

Study Evaluating the Safety and Efficacy of Astarabine in Acute Myeloid Leukemia or Acute Lymphoblastic Leukemia

NCT02544438 ↗

Phase 1/2 Completed 20 enrolled BioSight Ltd.
NaSingle-groupOpen-labelTreatment

Summary

A Phase I/IIa, open-label, uncontrolled study to evaluate the safety and efficacy of Astarabine (BST-236) as single agent in patients with refractory or relapsed Acute Myeloid Leukemia (AML) or Acute Lymphoblastic Leukemia (ALL) disease

Timeline

Start
2015-09
Primary completion
2017-09-20
Completion
2017-09-20

Drugs

EvaluationDrugModalityDoseRoute
Subject aspacytarabine Small molecule 0.3 g Intravenous
Subject aspacytarabine Small molecule 0.5 g Intravenous
Subject aspacytarabine Small molecule 0.8 g Intravenous
Subject aspacytarabine Small molecule 1.5 g Intravenous
Subject aspacytarabine Small molecule 2.3 g Intravenous
Subject aspacytarabine Small molecule 3 g Intravenous
Subject aspacytarabine Small molecule 4.5 g Intravenous
Subject aspacytarabine Small molecule 6 g Intravenous