The study will assess the role of high-dose imatinib mesylate, in patients who have taken imatinib mesylate for at least 1 year at the standard dose, in achieving a major molecular response (a measure of the level of chronic myelogenous leukemia) versus the standard dose.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
80
Novartis Investigative Site
Toronto, Canada
Percent of patients achieving major molecular response at baseline and at last visit
Complete cytogenetic response at baseline and at last visit
Overall survival
Disease progression-free survival
Quality of Life assessment at baseline, last visit
Safety: adverse events and lab parameters, vital signs, physical exam, electrocardiogram, concomitant medications
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