An Immuno-therapy Study to Evaluate the Effectiveness, Safety and Tolerability of Nivolumab or Nivolumab in Combination With Other Agents in Patients With Advanced Liver Cancer

Last updated:
2026-07-25
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View trial details

Overview

Official protocol title:

A PHASE I DOSE ESCALATION STUDY TO INVESTIGATE THE SAFETY, IMMUNOREGULATORY ACTIVITY, PHARMACOKINETICS, AND PRELIMINARY ANTITUMOR ACTIVITY OF ANTI-PROGRAMMED-DEATH-1 (PD-1) ANTIBODY (BMS-936558) IN ADVANCED HEPATOCELLULAR CARCINOMA IN SUBJECTS WITH OR WITHOUT CHRONIC VIRAL HEPATITIS

Intervention/treatment:
NIVOLUMAB / FLUDEOXYGLUCOSE 18F
Medical condition:
HEPATOCELLULAR CARCINOMA
Protocol code:
CA209-040
Control number:
182072
Status:
Closed
Approved:
March 13, 2015
Date Completed:
Trial phase:
Phase 1, Phase 2
For more information:
ClinicalTrials.gov - NCT01658878
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

Nova Scotia

Local Institution - 0065
Halifax, Nova Scotia, B4H 2Y9

Ontario

Local Institution - 0039
Toronto, Ontario, M5G 2M9

Quebec

Local Institution - 0022
Montreal, Quebec, H2X 3E4

Results

See the results from the trial NCT01658878. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
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