drugset / Trial / NCT01209286

Study of the BiTE® Blinatumomab (MT103) in Adult Patients With Relapsed/Refractory B-Precursor Acute Lymphoblastic Leukemia (ALL)

NCT01209286

Phase 2 Completed 36 enrolled Amgen Research (Munich) GmbH
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to determine whether the bispecific T-cell engager blinatumomab is effective, safe and tolerable in the treatment of patients with relapsed/refractory B-precursor ALL.

Timeline

Start
2010-10
Primary completion
2012-03
Completion
2016-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Blinatumomab Monoclonal antibody 15 ug/m2 Intravenous
Subject Blinatumomab Monoclonal antibody 30 ug/m2 Intravenous

Indications

No indication recorded.