Table 2.
Trial | Identifier | Phase | BCLC Stage | Treatment Arms | Primary Endpoint(s) | Setting |
---|---|---|---|---|---|---|
COSMIC-312 | NCT03755791 | Phase 3 | B or C | Cabozantinib + atezolizumab Sorafenib Cabozantinib |
PFS per RECIST 1.1 OS |
First-line |
LEAP-002 | NCT03713593 | Phase 3 | B or C | Lenvatinib + pembrolizumab Lenvatinib |
PFS per RECIST 1.1 OS |
First-line |
HIMALAYA | NCT03298451 | Phase 3 | B or C | Durvalumab Durvalumab + trevelimumab (2 regimens) Sorafenib |
OS | First-line |
CheckMate 9DW | NCT04039607 | Phase 3 | C | Nivolumab + ipilimumab Sorafenib or lenvatinib |
OS | First-line |
N/A | NCT03764293 | Phase 3 | B or C | Camrelizumab (SHR-1210) + apatinib Sorafenib |
PFS OS |
First-line |
RATIONALE-301 | NCT03412773 | Phase 3 | B or C | Tislelizumab Sorafenib |
OS | First-line |
GOING | NCT04170556 | Phase 1/2 | BCLC C | Regorafenib (monotherapy for the first 8 weeks) + nivolumab | Safety | Second-line |
RENOBATE | NCT04310709 | Phase 2 | B or C | Regorafenib + nivolumab | ORR per RECIST 1.1 | First-line |
Bayer 19497 | NCT03347292 | Phase 1b/2 | B or C | Regorafenib + pembrolizumab | Safety | First-line |
N/A | NCT04183088 | Phase 2 | B or C | Part 1: Regorafenib + tislelizumab Part 2: Regorafenib + tislelizumab Regorafenib |
Part 1: Safety Part 2: PFS per RECIST 1.1 ORR per RECIST 1.1 |
First-line |
N/A | NCT04442581 | Phase 2 | B or C | Cabozantinib + pembrolizumab | ORR per RECIST 1.1 | First-line |
N/A | NCT03941873 | Phase 1/2 | B or C | Phase 1: Sitravatinib Sitravatinib + tislelizumab Phase 2: Sitravatinib Sitravatinib + tislelizumab |
Phase 1: Safety Phase 2: ORR per RECIST 1.1 |
First- and later line |
BCLC, Barcelona Clinic Liver Cancer; ORR, overall response rate; OS, overall survival; PFS, progression-free survival; RECIST, Response Evaluation Criteria in Solid Tumours.