CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 145 enrolled
Drug / intervention
Nivolumab +1 morebiological
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02581631
NCT02581631Phase 2Completed

A Phase I/ II Study to Evaluate the Safety and Preliminary Efficacy of Nivolumab in Combination With Brentuximab Vedotin in Subjects With Relapsed Refractory Non Hodgkin Lymphomas With CD30 Expression (CheckMate 436: CHECKpoint Pathway and Nivolumab Clinical Trial Evaluation 436)

Bristol-Myers Squibb·interventional·Posted Oct 21, 2015·Updated Mar 7, 2023

In Brief

A Phase 2 clinical trial evaluating Nivolumab and Brentuximab Vedotin for Non-Hodgkin's Disease. Completed, enrolled 145 participants across 27 sites in 6 countries.

Detailed Summary

The purpose of this study is to determine whether Nivolumab, in combination with brentuximab vedotin, is safe and effective in patients with certain subtypes of non-Hodgkin's lymphomas with CD30 expression that have not responded to treatment or have come back. The subtypes we are studying are Diffuse Large B-Cell Lymphoma (DLBCL), Peripheral T-Cell Lymphoma (PTCL), Cutaneous T-Cell Lymphoma (CTCL), Primary Mediastinal Large B-Cell Lymphoma (PMBL) and Mediastinal Gray Zone Lymphoma (MGZL).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCanada, France, Italy, Spain, United Kingdom, United States
CollaboratorsSeagen Inc.

Timeline

Phase 2CompletedFinished
20162017201820192020202120222023202420252026
First PostedOct 21, 2015
Enrollment StartFeb 11, 2016
Primary CompletionJan 16, 2020
Study CompletionFeb 7, 2022
TodayJul 2, 2026
Enrollment to primary: 3.9 yearsPosted 10.7 years ago

Interventions

Nivolumabbiological

Brentuximab Vedotindrug