drugset / Trial / NCT00514488

Imatinib Standard Dose (400 mg/Day) Versus Imatinib High Dose (800 mg/Day)

NCT00514488 ↗

RandomizedParallel-groupOpen-label

Summary

This is a phase III multicenter, open-label study designed to investigate the efficacy (hematological response, cytogenetic response and molecular response) and feasibility (tolerance, compliance and safety) of the tyrosine kinase inhibitor imatinib mesylate (formerly STI 571, GLIVEC, Novartis Pharma) at conventional dose (400 mg/daily) if compared with high dose (800 mg/daily) (serial number protocol ICSG/CML/022) in patients with Ph+ chronic myeloid leukemia (CML) in chronic phase (CP) previously untreated, at high Sokal risk.

Timeline

Start
2004-06
Primary completion
—
Completion
—

Outcome

Missed primary endpoint

paper The CCgR rate at 1 year was 64% and 58% for the high-dose arm and for the standard-dose arm, respectively (P = .435). PMID 19264678 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Imatinib Small molecule 400 mg —
Subject Imatinib Small molecule 800 mg —