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Completed Phase 1Phase 2 Interventional Results available

An Investigational Immuno-therapy Safety and Effectiveness Study of Nivolumab in Combination With Brentuximab Vedotin to Treat Non-Hodgkin Lymphomas

ClinicalTrials.gov ID: NCT02581631

Public ClinicalTrials.gov record NCT02581631. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 11, 2026, 12:43 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

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)

Study identification

NCT ID
NCT02581631
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Bristol-Myers Squibb
Industry
Enrollment
145 participants

Conditions and interventions

Interventions

  • Brentuximab Vedotin Drug
  • Nivolumab Biological

Drug · Biological

Eligibility (public fields only)

Age range
15 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 10, 2016
Primary completion
Jan 15, 2020
Completion
Feb 6, 2022
Last update posted
Mar 6, 2023

2016 – 2022

United States locations

U.S. sites
16
U.S. states
13
U.S. cities
15
Facility City State ZIP Site status
Local Institution - 0017 Birmingham Alabama 35294-3300
University Of Miami Sylvester Comprehensive Cancer Center Miami Florida 33136
Local Institution - 0012 Tampa Florida 33612
Winship Cancer Institute. Atlanta Georgia 30322
University Of Chicago Chicago Illinois 60637
Mayo Clinic Rochester Minnesota 55905
Washington University School Of Medicine St Louis Missouri 63110
Local Institution - 0003 New York New York 10021
Local Institution - 0010 New York New York 10029
University Of Rochester Rochester New York 14642
Levine Cancer Institute Charlotte North Carolina 28204
The Ohio State University Comprehensive Cancer Center Columbus Ohio 43210
Stephenson Cancer Center Oklahoma City Oklahoma 73104
Providence Portland Medical Center Portland Oregon 97213
Bon Secours-St Francis Hosp Greenville South Carolina 29607
University of Washington - Seattle Cancer Care Alliance Seattle Washington 98109-1023

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 11 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02581631, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 6, 2023 · Synced May 11, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02581631 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →