drugset / Trial / NCT02467270

Ponatinib in Participants With Resistant Chronic Phase Chronic Myeloid Leukemia (CP-CML) to Characterize the Efficacy and Safety of a Range of Doses

NCT02467270

Phase 2 Completed 283 enrolled Takeda
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to characterize the efficacy of ponatinib administered in 3 starting doses (45 mg, 30 mg, and 15 mg daily) in participants with CP-CML who are resistant to prior tyrosine-kinase inhibitor (TKI) therapy or have T315I mutation, as measured by \<=1 % Breakpoint Cluster Region-Abelson Transcript Level using International Scale (BCR-ABL1IS) at 12 months.

Timeline

Start
2015-07-13
Primary completion
2020-04-29
Completion
2025-04-23

Drugs

EvaluationDrugModalityDoseRoute
Subject Ponatinib Small molecule 15 mg Oral
Subject Ponatinib Small molecule 30 mg Oral
Subject Ponatinib Small molecule 45 mg Oral