drugset / Trial / NCT01874054

Study of Brentuximab Vedotin Combined With Bendamustine in Patients With Hodgkin Lymphoma

NCT01874054

Phase 1/2 Completed 55 enrolled Seagen Inc.
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to assess safety and efficacy of brentuximab vedotin in combination with bendamustine in patients with relapsed or refractory Hodgkin lymphoma. It is an open-label, 2-stage study designed to determine the recommended dose level of bendamustine in combination with brentuximab vedotin. The study will assess the safety profile of the combination treatment and determine what proportion of patients achieve a complete remission.

Timeline

Start
2013-06
Primary completion
2015-12
Completion
2018-02-20

Drugs

EvaluationDrugModalityDoseRoute
Subject Bendamustine Small molecule 90 mg/m2 Intravenous
Subject Brentuximab Vedotin Monoclonal antibody 1.8 mg/kg Intravenous

Indications