Overview

Trial of CPX-351 in Adult Patients With First Relapse Acute Myeloid Leukemia (AML)

Status:
Completed
Trial end date:
2012-01-01
Target enrollment:
Participant gender:
Summary
The study investigates if CPX-351 will be a) more effective than the standard intensive salvage AML treatment and b) more tolerable than the standard intensive salvage treatment regimens. The study compares the investigational product CPX-351 vs the standard intensive salvage treatment for first relapse AML patients.
Phase:
Phase 2
Details
Lead Sponsor:
Celator Pharmaceuticals
Jazz Pharmaceuticals
Collaborator:
The Leukemia and Lymphoma Society
Treatments:
Cytarabine