Table 2.
Studies of Immune Checkpoint Inhibitor PD-1/PD-L1 and CTLA4 from Clinicaltrials.gov (Accessed 15th April 2020)
| Clinical Trial Identifier | Agent | Immune Target | Primary Endpoint | Sample Size | Statusa | Phaseb |
|---|---|---|---|---|---|---|
| NCT01693783 | Ipilimumab | CTLA-4 | response rate | n=44 | ongoing | 2 |
| NCT01711515 | Ipilimumab | CTLA-4 | Toxicity | n=34 | ongoing | 1 |
| NCT01975831 | Tremelimumab, Durvalumab (MEDI4736) | CTLA-4, PD-L1 | Adverse event | n=106 (include other cancers) | ongoing | 1 |
| NCT02257528 | Nivolumab | PD-1 | response rate | n=26 | ongoing | 2 |
| NCT02725489 | Durvalumab VS Vigil | PD-L1 | Adverse event | n=13 (include other cancers) | ongoing | 2 |
| NCT02914470 | Atezoluzumab | PD-L1 | Toxicity | n=12 (include other cancers) | ongoing | 1 |
| NCT02921269 | Atezoluzumab | PD-L1 | Response rate | n=22 | ongoing | 2 |
| NCT03073525 | Atezoluzumab VS Vigil | PD-L1 | Adverse event | n=25 (include other cancers) | ongoing | 2 |
| NCT03104699 | AGEN2034 | PD-1 | Response rate | n=150 | ongoing | 1, 2 |
| NCT03635567 | Pembrolizumab (MK-3475) VS chemotherapy | PD-1 | Overall survival | n=600 | ongoing | 3 |
Notes: aStatus can be divided into recruit, ongoing, terminated, completed. bClinical phase can be divided into 1, 2, 3, 4.