Active, not recruitingPhase 1NCT04658147
Feasibility and Efficacy of Perioperative Nivolumab With or Without Relatlimab for Patients With Potentially Resectable Hepatocellular Carcinoma (HCC)
Studying Adult hepatocellular carcinoma
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
- Principal Investigator
- Mark Yarchoan, MDSKCCC Johns Hopkins Medical Institution
- Intervention
- Nivolumab(drug)
- Enrollment
- 31 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2021 – 2030
Study locations (2)
- Sidney Kimmel Comprehensive Cancer Center, Baltimore, Maryland, United States
- The Ohio State University, Wexner Medical Center, Columbus, Ohio, United States
Collaborators
Bristol-Myers Squibb
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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