drugset / Trial / NCT00050531

High-Dose Gleevec Alone or in Combination With Peg-Intron and GM-CSF in Early Phase Chronic Myelogenous Leukemia (CML)

NCT00050531

Phase 3 Completed 94 enrolled M.D. Anderson Cancer Center Novartis · collab
RandomizedCrossoverOpen-labelTreatment

Summary

The goal of this clinical research study is to learn if giving PEG-Alpha Interferon (PEG-Intron) and Sargramostim (GM-CSF) to patients receiving treatment with high dose Gleevec (imatinib mesylate) is more effective in treating CML in chronic phase than therapy with imatinib mesylate alone.

Timeline

Start
2003-04
Primary completion
2007-04
Completion
2015-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Peginterferon alfa-2b Protein / enzyme biologic 0.5 ug/kg Subcutaneous
Subject sargramostim Protein / enzyme biologic 125 ug/m2 Subcutaneous
Background Imatinib Small molecule 400 mg Oral