drugset / Trial / NCT01399840

Study of BMN 673, a PARP Inhibitor, in Patients With Advanced Hematological Malignancies

NCT01399840

Phase 1 Completed 33 enrolled Pfizer Medivation, Inc. · collab
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This is a two-arm, open-label study to determine the maximum tolerated dose (MTD) and assess the safety, pharmacokinetics, pharmacodynamics, and preliminary efficacy of BMN 673 in patients with Acute Myeloid Leukemia (AML), Myelodysplastic Syndrome (MDS), Chronic Lymphocytic Leukemia (CLL) and Mantle Cell Lymphoma (MCL). Arm 1 will enroll patients with either AML or MDS; Arm 2 will enroll patients with either CLL or MCL.

Timeline

Start
2011-06-30
Primary completion
2014-03-31
Completion
2014-05-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Talazoparib Small molecule 0.1 mg Oral
Subject Talazoparib Small molecule 0.9 mg Oral
Subject Talazoparib Small molecule 2 mg Oral