CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 266 enrolled
Drug / intervention
Nivolumab +1 morebiological
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04567615
NCT04567615Phase 2Completed

A Phase 2, Randomized, Open-label Study of Relatlimab in Combination With Nivolumab in Participants With Advanced Hepatocellular Carcinoma Who Are Naive to IO Therapy But Progressed on Tyrosine Kinase Inhibitors (RELATIVITY-073)

Bristol-Myers Squibb·interventional·Posted Sep 28, 2020·Updated Jan 8, 2026

In Brief

A Phase 2 clinical trial evaluating Nivolumab and Relatlimab for Hepatocellular Carcinoma and 4 related conditions. Completed, enrolled 266 participants across 65 sites in 17 countries.

Detailed Summary

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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesArgentina, Brazil, Chile, China, Czechia, France, Hong Kong, Japan, Mexico, New Zealand, Poland, Romania, Singapore, South Korea, Spain, Taiwan, Turkey (Türkiye)
Collaborators--

Timeline

Phase 2CompletedFinished
202120222023202420252026
First PostedSep 28, 2020
Enrollment StartFeb 4, 2021
Primary CompletionAug 31, 2023
Study CompletionNov 19, 2025
TodayJul 2, 2026
Enrollment to primary: 2.6 yearsPosted 5.8 years ago

Interventions

Nivolumabbiological

Specified dose on specified days

Relatlimabbiological

Specified dose on specified days