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Completed Phase 1 Interventional

Combination Study of Urelumab and Rituximab in Patients With B-cell Non-Hodgkins Lymphoma

ClinicalTrials.gov ID: NCT01775631

Public ClinicalTrials.gov record NCT01775631. 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 Oct 19, 2026, 7:46 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 1b, Open-label, Multicenter Study of Urelumab (BMS-663513) in Combination With Rituximab in Subjects With Relapsed/Refractory B-cell Malignancies

Brief summary

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

The purpose of the study is to determine the safety, tolerability and maximum tolerated dose of Urelumab in combination with Rituximab in patients with B-cell Non-Hodgkins Lymphoma

Study identification

NCT ID
NCT01775631
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Bristol-Myers Squibb
Industry
Enrollment
47 participants

Conditions and interventions

Interventions

Biological

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 2013 (Type not available)
Primary completion
Aug 2016 (Actual)
Completion
Aug 2016 (Actual)
Last update posted
Mar 31, 2017

2013 – 2016

United States locations

U.S. sites
15
U.S. states
12
U.S. cities
15
Facility City State ZIP Site status
Ucla Department Of Medicine Los Angeles California 90095 —
Stanford University Medical Center Stanford California 94305 —
University Of Miami Sylvester Comprehensive Cancer Center Miami Florida 33136 —
Mount Sinai Comprehensive Cancer Center Miami Beach Florida 33140 —
University Of Iowa Hospitals And Clinics Iowa City Iowa 52242 —
Dana Faber Cancer Institute Boston Massachusetts 02215 —
University Of Michigan Health System Ann Arbor Michigan 48109 —
Karmanos Cancer Institute Detroit Michigan 48201 —
John Theurer Cancer Center Hackensack New Jersey 07601 —
Memorial Sloan Kettering Cancer Center New York New York 11065 —
Levine Cancer Institute Charlotte North Carolina 28204 —
Providence Cancer Center Oncology And Hematology Care- Eastside Portland Oregon 97213 —
Hospital Of The University Of Pennsylvania Philadelphia Pennsylvania 19104 —
The University Of Texas Md Anderson Cancer Center Houston Texas 77030 —
University Of Virginia School Of Medicine Charlottesville Virginia 22908 —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01775631, 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 31, 2017 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01775631 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →