CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 657 enrolled
Drug / intervention
Nivolumab +3 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/NCT01658878
NCT01658878Phase 2Completed

A Phase 1/2, Dose-escalation, Open-label, Non-comparative Study of Nivolumab or Nivolumab in Combination With Ipilimumab in Advanced Hepatocellular Carcinoma Subjects With or Without Chronic Viral Hepatitis; and a Randomized, Open-label Study of Nivolumab vs Sorafenib in Advanced Hepatocellular Carcinoma Subjects Who Are Naive to Systemic Therapy

Bristol-Myers Squibb·interventional·Posted Aug 7, 2012·Updated Dec 24, 2025

In Brief

A Phase 2 clinical trial evaluating Nivolumab, Sorafenib, and 2 other interventions for Hepatocellular Carcinoma. Completed, enrolled 657 participants across 60 sites in 13 countries.

Detailed Summary

The first part of the study is the Dose Escalation Phase designed to establish the safety of nivolumab at different dose levels for each of the three cohorts (uninfected hepatocellular carcinoma (HCC) subjects, hepatitis C virus (HCV)-infected HCC subjects, and hepatitis B virus (HBV)-infected subjects). The second part of the study is the Expansion Phase designed to generate additional clinical data at specified doses for each of the 3 cohorts. A third cohort has been added in this study to compare the efficacy of nivolumab and sorafenib in the treatment of Advanced HCC. A fourth cohort will generate data on the safety and efficacy of the combination nivolumab plus ipilimumab in the treatment of Advanced HCC. In the fifth cohort, additional clinical data will be generated for Child-Pugh B subjects. A Cabozantinib Combination Cohort has been added to evaluate the safety and tolerability of nivolumab in combination with cabozantinib and nivolumab with ipilimumab in combination with cabozantinib.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCanada, France, Germany, Hong Kong, Italy, Japan, Puerto Rico, Singapore, South Korea, Spain, Taiwan, United Kingdom, United States

Timeline

Phase 2CompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedAug 7, 2012
Enrollment StartOct 30, 2012
Primary CompletionNov 12, 2024
TodayJul 2, 2026
Enrollment to primary: 12.0 yearsPosted 13.9 years ago

Interventions

Nivolumabbiological

Sorafenibdrug

Ipilimumabdrug

Cabozantinibdrug