Safety and Bioactivity of Ipilimumab and Nivolumab Combination Prior to Liver Resection in Hepatocellular Carcinoma
Phase 1/2
Completed
NCT03682276
| Condition | Hepatocellular Carcinoma |
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| Phase | Phase 1/2 |
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| Sponsor | Imperial College London |
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| Status | Completed |
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| Enrollment | 33 participants |
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| Interventions | Ipilimumab, Nivolumab |
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| Start date | Mar 1, 2019 |
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| Completion date | Mar 12, 2026 |
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| Results posted | Jun 29, 2026 |
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Summary
The PRIME-HCC trial will assess the effects of combination treatment with nivolumab (OPDIVO) and ipilimumab (YERVOY) pre-operatively in hepatocellular carcinoma patients for whom liver resection is planned. The trial will be conducted at a small number of National Health Service hospitals in the UK. Participants will receive two doses of nivolumab and a single dose of ipilimumab in the weeks before their planned surgery.
Delay to Surgery
Up to Day 89 · Participants
| Treatment Group | 2 Participants |
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Frequency of Treatment-related Adverse Events [Safety and Tolerability]
Up to Day 127 · Participants
| Treatment Group | 25 Participants |
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Open in BENITIONS
View on ClinicalTrials.gov
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