Clinical trial

An Immuno-therapy Study to Evaluate the Effectiveness, Safety and Tolerability…

NCT01658878 · Bristol-Myers Squibb, Industry · Completed

Key facts

NCT number NCT01658878
Title 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
Official title 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…
Acronym CheckMate040
Lead sponsor Bristol-Myers Squibb, Industry
Collaborators Ono Pharmaceutical Co. Ltd Industry
Status Completed
Phase Phase 1/Phase 2
Study type Interventional
Conditions Hepatocellular Carcinoma
Intervention type Biological, Drug
Interventions Nivolumab, Sorafenib, Ipilimumab, Cabozantinib
Enrollment 657
Start date Oct 30, 2012
Primary completion Nov 12, 2024
Completion Nov 12, 2024
First posted Aug 7, 2012
Last update posted Dec 24, 2025
Countries Canada, France, Germany, Hong Kong, Italy, Japan, Puerto Rico, Singapore, South Korea, Spain, Taiwan, United Kingdom and 1 more

At a glance

  • 10–99 Study sites
  • Yes Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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