drugset / Trial / NCT02927769

A Study of Nivolumab Plus Brentuximab Vedotin in Patients Between 5 and 30 Years Old, With Hodgkin's Lymphoma (cHL), Relapsed or Refractory From First Line Treatment

NCT02927769

Phase 2 Completed 72 enrolled Bristol-Myers Squibb Seagen Inc. · collab
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to determine whether nivolumab plus brentuximab vedotin (followed by brentuximab vedotin plus bendamustine in patient with suboptimal response) is safe and effective in treating patients with Hodgkin's lymphoma (cHL). Eligible patients are children, adolescents, and young adults relapsed or refractory to first line.

Timeline

Start
2017-03-28
Primary completion
2024-05-28
Completion
2024-05-28

Drugs

EvaluationDrugModalityDoseRoute
Subject Bendamustine Small molecule
Subject Brentuximab Vedotin Monoclonal antibody
Subject Nivolumab Monoclonal antibody

Indications