drugset / Trial / NCT00333840

Safety and Efficacy of Imatinib Versus Interferon-α Plus Cytarabine in Patients With Newly Diagnosed Philadelphia Chromosome Positive Chronic Myelogenous Leukemia

NCT00333840

Phase 3 Completed 1106 enrolled Novartis Pharmaceuticals
RandomizedCrossoverOpen-labelTreatment

Summary

The purpose of this study is to evaluate and compare the side effects and anti-leukemic benefits of imatinib with those of interferon and Ara-C for patients who have chronic myeloid leukemia (CML) in the chronic phase. Patients in this study will be randomized (1:1) to receive either interferon plus Ara-C or imatinib as initial treatment.

Timeline

Start
2000-06
Primary completion
2012-03
Completion
2012-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Cytarabine Small molecule 20 mg/m2 Subcutaneous
Subject Imatinib Small molecule 400 mg Oral
Subject interferon alfa-2b Protein / enzyme biologic 5 unknown Subcutaneous