drugset / Trial / NCT01222013

Study for Safety and Efficacy Evaluation of Imatinib Mesylate in Children With Acute Lymphoblastic Leukemia (ALL) Philadelphia Chromosome-positive (Ph+)

NCT01222013 ↗

Phase 2 Suspended 20 enrolled Renato Melaragno
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the efficacy, through molecular response and event-free survival, about the use of Imatinib in conjunction with chemotherapy after BFM "like" Induction in children with ALL Ph+.

Timeline

Start
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Primary completion
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Completion
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Outcome

Outcome not reported

Stopped (Enrollment): “Study was suspended before recruitment, due to logistic issues.”

Drugs

EvaluationDrugModalityDoseRoute
Subject Imatinib Small molecule 300 mg/m2 Oral