drugset / Trial / NCT01647971

Study of the Efficacy and Safety of Ublituximab in Patients With Relapsed or Refractory B-cell Non-Hodgkin Lymphoma

NCT01647971

Phase 1/2 Completed 39 enrolled TG Therapeutics, Inc.
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine whether ublituximab is safe and effective in patients with relapsed or refractory B-cell lymphoma who were previously treated with rituximab.

Timeline

Start
2012-07-19
Primary completion
2015-05
Completion
2015-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Ublituximab Monoclonal antibody 600 mg Intravenous
Subject Ublituximab Monoclonal antibody 900 mg Intravenous
Subject Ublituximab Monoclonal antibody 1200 mg Intravenous