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Completed Phase 2 Interventional Results available

Study of Nivolumab in Subjects With Relapsed or Refractory Follicular Lymphoma (FL) (CheckMate 140)

ClinicalTrials.gov ID: NCT02038946

Public ClinicalTrials.gov record NCT02038946. 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 Sep 8, 2026, 5:12 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 Single Arm, Open-Label Phase 2 Study of Nivolumab (BMS-936558) in Subjects With Relapsed or Refractory Follicular Lymphoma (FL)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to assess the clinical benefit of Nivolumab, as measured by independent radiologic review committee (IRRC)-assessed objective response rate (ORR) in subjects with FL lymphoma who have failed therapy with both CD20 antibody and an alkylating agent.

Study identification

NCT ID
NCT02038946
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Bristol-Myers Squibb
Industry
Enrollment
116 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 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
Mar 25, 2014
Primary completion
May 16, 2017
Completion
Dec 27, 2020
Last update posted
Jan 3, 2022

2014 – 2020

United States locations

U.S. sites
12
U.S. states
10
U.S. cities
10
Facility City State ZIP Site status
Mayo Clinic Arizona Phoenix Arizona 85054
Division Of Hematology & Oncology Ctr. For Health Sciences Los Angeles California 90095
Winship Cancer Institute. Atlanta Georgia 30322
Beth Israel Deaconess Medical Center (BIDMC) Boston Massachusetts 02215
Dana Farber Cancer Institute Boston Massachusetts 02215
Massachusetts General Hospital Boston Massachusetts 02215
Mayo Clinic Rochester Minnesota 55905
Weill Cornell Medical College New York New York 10021
Duke University Medical Center Durham North Carolina 27710
Vanderbilt University Medical Center Nashville Tennessee 37232
MD Anderson Cancer Center Houston Texas 77030
Huntsman Cancer Institute Salt Lake City Utah 84112

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 33 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02038946, 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 Jan 3, 2022 · Synced Sep 8, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02038946 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →