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. 2022 Jun 30;13:907591. doi: 10.3389/fimmu.2022.907591

Table 1.

Immune checkpoint inhibitors approved by US and European regulatory authorities.

AGENT TARGET INDICATION FDA approval EMA approval
atezolizumab (Tecentriq) PD-L1 melanoma, small cell and non-small cell lung cancer, hepatocellular carcinoma. urothelial carcinoma 2016 2017
ipilimumab (Yervoy) CTLA-4 Melanoma, renal cell carcinoma, MSI high or MMR deficient colorectal cancer, hepatocellular carcinoma, non-small cell lung cancer, mesothelioma 2011 2011
nivolumab (Opdivo) PD-1 melanoma, renal cell cancer, non-small cell lung cancer, Hepatocellular carcinoma, Head and neck squamous cell carcinoma, urothelial carcinoma, esophageal or gastric cancer, colorectal cancer, Hodgkin lymphoma, mesothelioma 2014 2015
pembrolizumab (Keytruda) PD-L1 melanoma, non-small cell lung cancer, head and neck squamous cell carcinoma, urothelial carcinoma, gastric adenocarcinoma, MSI high or MMR deficient colorectal cancer, Hodgkin lymphoma, cervical cancer, renal carcinoma, Merkel cell carcinoma, cutaneous squamous cell carcinoma, triple-negative breast cancer 2014 2015
Avelumab (Bavencio) PD-L1 Merkel Cell Carcinoma, urothelial carcinoma, renal cell carcinoma 2017 2017
Durvalumab (Imfinzi) PD-L1 Small cell and non-small cell lung cancer 2017 2018
Cemiplimab (Libtayo) PD-1 Non-small cell lung cancer, cutaneous squamous cell carcinoma, Basal cell carcinoma 2018 2019

FDA, United States Federal Drug Administration; EMA, European Medicines Agency; PD-1, Programmed cell death protein 1; PD-L1, Programmed death-ligand 1, CTLA-4; Cytotoxic T-lymphocyte associated protein 4, MSI; Microsatellite instability, MMR; mismatch repair.