For Healthcare Professionals

A Study of Relatlimab in Combination With Nivolumab in Participants With Advanced Liver Cancer Who Have Never Been Treated With Immuno-oncology Therapy After Prior Treatment With Tyrosine Kinase Inhibitors

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About the study

The purpose of this study is to evaluate the effectiveness and safety of relatlimab in combination with nivolumab in participants with advanced liver cancer who have never been treated with immuno-oncology therapy, after prior treatment with tyrosine kinase inhibitor therapy.
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Who can take part

You may be eligible to participate in the study if you meet the following criteria:

INCLUSION CRITERIA

Key Inclusion Criteria:


  1. Must have a diagnosis of hepatocellular carcinoma (HCC) based on histological confirmation
  2. Must have advanced/metastatic HCC
  3. Have to be immunotherapy treatment-naive in the advanced/metastatic setting
  4. Must have at least one Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 measurable untreated lesion
  5. Child-Pugh score of 5 or 6
  6. Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1 for ECOG performance status scale

EXCLUSION CRITERIA

Key Exclusion Criteria:


  1. Known fibrolamellar HCC, sarcomatoid HCC, combined hepatocellular cholangiocarcinoma
  2. Prior organ allograft or allogeneic bone marrow transplantation
  3. No uncontrolled or significant cardiovascular disease
  4. No active known autoimmune disease
  5. Have received one or two lines of tyrosine kinase inhibitor therapies
  6. Evidence of radiographic progression on or after the last line of tyrosine kinase inhibitor therapy

Other protocol-defined inclusion/exclusion criteria apply


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Study Locations

Enter your ZIP code/Postal code/PIN code to locate study sites near you:

How to Apply


Contact the study center to learn if this study is a good match for you.

Study’s details


Contition

Hepatocellular Carcinoma,Hepatoma,Liver Cancer, Adult,Liver Cell Carcinoma,Liver Cell Carcinoma, Adult

Age (in years)

18+

Phase

Phase 2

Participants needed

266

Est. Completion Date

Jan 31, 2025

Treatment type

Interventional


Sponsor

Bristol-Myers Squibb

ClinicalTrials.gov identifier

NCT04567615

Study number

CA224073

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