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. 2020 Aug 12;13:8037–8047. doi: 10.2147/OTT.S264312

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.