drugset / Trial / NCT02544438
Study Evaluating the Safety and Efficacy of Astarabine in Acute Myeloid Leukemia or Acute Lymphoblastic Leukemia
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |