A Study to Evaluate the Safety, Tolerability, and Efficacy of Relatlimab in Relapsed or Refractory B-Cell Malignancies

Last updated:
2026-07-25
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View trial details

Overview

Official protocol title:

A PHASE 1/2A DOSE ESCALATION AND COHORT EXPANSION STUDY OF THE SAFETY, TOLERABILITY, AND EFFICACY OF ANTI-LAG-3 MONOCLONAL ANTIBODY (BMS-986016) ADMINISTERED ALONE AND IN COMBINATION WITH ANTI-PD-1 MONOCLONAL ANTIBODY (NIVOLUMAB, BMS-936558) IN RELAPSED OR REFRACTORY B-CELL MALIGNANCIES

Intervention/treatment:
OPDIVO
Medical condition:
B-CELL MALIGNANCIES
Protocol code:
CA224-022
Control number:
211104
Status:
Closed
Approved:
December 08, 2017
Date Completed:
Trial phase:
Phase 1, Phase 2
For more information:
ClinicalTrials.gov - NCT02061761
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
18 Years and older
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
Bristol-Myers Squibb Study Director
Organization
Bristol-Myers Squibb
Phone:
Please Email
Sponsor
BRISTOL-MYERS SQUIBB CANADA

Locations

British Columbia

Local Institution - 0011
Vancouver, British Columbia, V5Z 4E6

Ontario

Local Institution - 0012
Toronto, Ontario, M5G 2M9

Results

See the results from the trial NCT02061761. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
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