Table 1.
Trial identifier | Line | Agents | Primary endpoint | Patients | Status |
---|---|---|---|---|---|
NCT03713593 | First line | Lenvatinib + pembrolizumab vs. lenvatinib | PFS, OS | 750 | Ongoing |
NCT03764293 | First Line | PD-1 antibody SHR-1210 + apatinib mesylate vs. sorafenib | PFS, OS | 510 | Ongoing |
NCT03298451 | First line | Durvalumab vs. durvalumab + tremelimumab vs. sorafenib | OS | 1,310 | Active, not recruiting |
NCT03412773 | First line | BGB-A317 (PD-1 antibody) vs. sorafenib | OS | 674 | Active, not recruiting |
NCT03434379 | First line | Atezolizumab + bevacizumab vs. sorafenib | OS, PFS | 480 | Active, not recruiting |
NCT01658878 | First line | Nivolumab + cabozantinib vs. nivolumab + ipilimumab + cabozantinib | Safety, tolerability and ORR | 1,097 | Active, not recruiting |
NCT03347292 | First line | Pembrolizumab + regorafenib | TEAEs, DLTs | 57 | Ongoing, recruiting |
NCT03439891 | First line | Nivolumab + sorafenib | MTD, ORR | 40 | Ongoing, recruiting |
PFS, progression free survival; OS, overall survival; TTP, time to progression; TR-RECIST, tumor response using Response Evaluation Criteria in Solid Tumors (RECIST); ORR, objective response rate; TEAEs, treatment-emergent adverse events; DLTs, dose limiting toxicities; MTD, maximum tolerated dose.