drugset / Trial / NCT02181738

Study of Nivolumab in Patients With Classical Hodgkin's Lymphoma (Registrational)

NCT02181738

Phase 2 Completed 294 enrolled Bristol-Myers Squibb
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of Nivolumab in previously treated (cohorts, A, B \& C) or newly diagnosed (cohort D) classical Hodgkin Lymphoma participants.

Timeline

Start
2014-08-12
Primary completion
2017-08-31
Completion
2022-12-27

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Nivolumab Monoclonal antibody 3 mg/kg Intravenous
Subject Nivolumab Monoclonal antibody 240 mg Intravenous
Background Dacarbazine Small molecule
Background Doxorubicin Other / unclassified
Background Vinblastine Small molecule

Indications