drugset / Trial / NCT01207388

Confirmatory Phase II Study of Blinatumomab (MT103) in Patients With Minimal Residual Disease of B-precursor Acute Lymphoblastic Leukemia (ALL)

NCT01207388

Phase 2 Completed 116 enrolled Amgen Research (Munich) GmbH
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to confirm whether the bispecific T cell engager blinatumomab (MT103) is effective, safe and tolerable in the treatment of ALL patients with minimal residual disease.

Timeline

Start
2010-11
Primary completion
2014-02
Completion
2019-01-07

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Blinatumomab Monoclonal antibody 15 ug/m2 Intravenous