Table 1. Clinical trials currently available with immune checkpoint inhibitors in HCC.
ClinicalTrials.gov identifier | Agent(s) | Target | Locoregional therapy | Study design | First or second line |
---|---|---|---|---|---|
NCT02795429 | PDR001/INC280 | PD-1/cMET | None | Ib/II | Second line |
NCT02702401 | Pembrolizumab | PD-1 | None | III | Second line |
NCT02702414 | Pembrolizumab | PD-1 | None | II | Second line |
NCT02856425 | Pembrolizumab/Nintedanib | PD-1/VEGFR, PDGFR, FGFR | None | I | Second line |
NCT02821754 | Tremelimumab/Durvalumab | CTLA-4/PD-L1 | RFA/TACE/Cryoablation | Pilot | Second line |
NCT02988440 | PDR001/Sorafenib | PD-1/Raf, VEGFR, PDGFR | None | Ib | First line |
NCT02989922 | SHR-1210 | PD-1 | None | II/III | Second line |
NCT02576509 | Nivolumab/Sorafenib | PD-1/Raf, VEGFR, PDGFR | None | III | First line |
NCT03033446 | Nivolumab | PD-1 | Radioembolization | II | First line |
NCT02859324 | CC-122/Nivolumab | CRBN/PD-1 | None | I/II | Second line |
NCT02423343 | Galunisertib/Nivolumab | TGF-β1/PD-1 | None | Ib/II | Second line |
NCT01658878 | Nivolumab/Ipilimumab | PD-1/CTLA-4 | None | I/II | First and second line |
NCT02837029 | Nivolumab | PD-1 | Yttrium microspheres | I/Ib | First and second line |
NCT01853618 | Tremelimumab | CTLA-4 | RFA/TACE/SBRT/Cryoablation | Pilot | Second line |
HCC, hepatocellular carcinoma; PD-1, programmed death 1; CTLA-4, cytotoxic T lymphocyte associated protein 4; VEGF, vascular endothelial growth factor; PDGFR, platelet-derived growth factor receptor; FGFR, fibroblast growth factor receptor; TGF-β, transforming growth factor β; RFA, radiofrequency ablation; TACE, transarterial chemoembolization; SBRT, stereotactic body radiation therapy.