drugset / Trial / NCT02228382

Safety And Efficacy Study Of Bosutinib In Patients With Philadelphia Chromosome Positive Chronic Myeloid Leukemia Previously Treated With One Or More Tyrosine Kinase Inhibitors

NCT02228382

NaOpen-labelTreatment

Summary

The purpose of this study is to fulfill the post-authorization commitment made by Pfizer to the European Medicines Agency in providing additional safety and efficacy data in approximately 150 Philadelphia Chromosome Positive Chronic Myeloid Leukemia patients with high unmet medical need, including 75 Chronic Phase, Accelerated Phase or Blast Phase patients in the fourth or later line treatment setting (i.e., after treatment with at least 3 other Tyrosine Kinase Inhibitors).

Timeline

Start
2014-11-07
Primary completion
2020-10-13
Completion
2020-10-13

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Bosutinib Small molecule 500 mg Oral