drugset / Trial / NCT01126814

A Study of Imatinib With Reinduction Chemotherapy Using Mitoxantrone, Etoposide and Cytarabine in Patients With Relapsed/Refractory C-kit Positive (AML) Acute Myeloid Leukemia

NCT01126814

Phase 1/2 Completed 35 enrolled University Health Network, Toronto
NaSingle-groupOpen-labelTreatment

Summary

This is a Phase I-II study evaluating the toxicity and efficacy of imatinib combined with mitoxantrone, etoposide and high-dose cytarabine reinduction therapy in relapsed and refractory AML. Patients will be treated initially at a 200 mg dose of imatinib; if tolerated, the imatinib dose will be escalated in subsequent cohorts to 300 mg and 400 mg. Once the recommended dose is determined, the remaining patients will be treated at that dose, to evaluate the antileukemic activity of the regimen. Patients achieving complete remission will receive consolidation therapy with imatinib combined with high-dose cytarabine and mitoxantrone, followed by maintenance imatinib.

Timeline

Start
2004-07
Primary completion
2009-09
Completion
2010-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Imatinib Small molecule 100 mg Oral
Subject Imatinib Small molecule 200 mg Oral
Subject Imatinib Small molecule 300 mg Oral
Subject Imatinib Small molecule 400 mg Oral

Indications