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Study Evaluating the Safety and Efficacy of Astarabine in Acute Myeloid Leukemia or Acute Lymphoblastic Leukemia — BSTPHASE1-01  

Acute Myeloid Leukemia Clinical Trial

Official title:
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

Clinical Trial 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

Clinical Trial Description

This is prospective, Phase I/IIa, open-label, uncontrolled, single-center, single arm study to evaluate the safety and efficacy of Astarabine given intravenously (I.V.) in escalated doses for 6 days for cycle in patients with relapsed or refractory AML or ALL who are more than 18 years of age. Patients will be screened for eligibility based on existing records and/or specific laboratory examinations performed for the screening process.

Patients will be gradually enrolled into 4 subsequent cohorts of escalating drug doses:

Cohort # Astarabine Dose Number of Patients

1. 0.5 gr/m2 (0.3 age>50) 3

2. 1.5 gr/m2 (0.8age>50) 3

3. 3.0 gr/m2 (1.5 age>50) 3

4. 4.5 gr/m2 (2.3 age>50) 6

5. 4.5 gr/m2 (no age limit) 3 up to 6

6. 6 gr/m2 (no age limit) 3 up to 6

Maximal tolerated dose (MTD) will be defined in case 2 subjects will experience a dose limiting toxicity (DLT) ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02544438
Study type Interventional
Source BioSight Ltd.
Contact
Status Completed
Phase Phase 1/Phase 2
Start date September 2015
Completion date September 20, 2017
View Details
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