drugset / Trial / NCT01684150

A Phase 1, Open-Label, Dose-Escalation & Expanded Cohort, Continuous IV Infusion, Multi-center Study of the Safety, Tolerability,PK & PD of EPZ-5676 in Treatment Relapsed/Refractory Patients With Leukemias Involving

NCT01684150

Phase 1 Completed 51 enrolled Epizyme, Inc. Celgene Corporation · collab
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the safe dose of EPZ-5676, to evaluate the safety of EPZ-5676 in patients with advanced hematologic malignancies, and to conduct a preliminary assessment of the anti-leukemia activity of EPZ-5676 in patients with acute leukemias bearing rearrangements of the MLL gene. Currently this study is in the MLL-r restricted/expansion phase and is only enrolling patients with rearrangements involving the MLL gene, including 11q23 or partial tandem duplications (PTD).

Timeline

Start
2012-09
Primary completion
2015-11
Completion
2016-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Pinometostat Small molecule 54 mg/m2 Intravenous
Subject Pinometostat Small molecule 90 mg/m2 Intravenous