drugset / Trial / NCT01317901

A Study of TRU-016 in Combination With Rituximab and Bendamustine in Subjects With Relapsed Indolent Lymphoma

NCT01317901

Phase 1 Completed 12 enrolled Aptevo Therapeutics
NaSingle-groupOpen-labelTreatment

Summary

This was a Phase 1 multicenter study of bendamustine, rituximab and TRU-016 (BRT) in subjects with relapsed indolent B-cell lymphoma. This was a multiple-dose escalation study to determine the maximum-tolerated dose (MTD) of TRU-016 given in combination with rituximab and bendamustine and to determine a safe dosing regimen for the combination in up to 12 subjects with relapsed indolent lymphoma. The originally planned Phase 2 portion, an open-label, randomized study to evaluate the efficacy of BRT compared with BR, was not conducted.

Timeline

Start
2011-05
Primary completion
2013-04
Completion
2013-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Otlertuzumab Monoclonal antibody 6 mg/kg Intravenous
Subject Otlertuzumab Monoclonal antibody 10 mg/kg Intravenous
Subject Otlertuzumab Monoclonal antibody 20 mg/kg Intravenous
Background Bendamustine Small molecule 90 mg/m2 Intravenous
Background Rituximab Monoclonal antibody 375 mg/m2 Intravenous