Table 1.
ICIs approved by the US FDA, 2011–21
Drug category | Generic name | Brand name | Approval date | Patent expiry | Manufacturer |
---|---|---|---|---|---|
CTLA-4 inhibitor | Ipilimumab | Yervoy® | 3/25/2011 | 2023 [41] | Bristol Myers Squibb |
PD-1 inhibitor | Pembrolizumab | Keytruda® | 9/4/2014 | 2036 [41] | Merck |
PD-1 inhibitor | Nivolumab | Opdivo® | 12/22/2014 | 2027 [41] | Bristol Myers Squibb |
PD-L1 inhibitor | Atezolizumab | Tecentriq® | 5/18/2016 | 2028 [41] | Genentech |
PD-L1 inhibitor | Avelumab | Bavencio® | 3/23/2017 | 2033 [42] | Merck, Pfizer |
PD-L1 inhibitor | Durvalumab | Imfinzi® | 5/1/2017 | 2030 [43] | AstraZeneca |
PD-1 inhibitor | Cemiplimab | Libtayo® | 9/28/2018 | 2035 [44] | Regeneron, Sanofi |
The above table describes the drug category, generic and brand names, approval date, patent expiry date, and manufacturers of individual ICIs. Approval dates and patent expiry dates in the table are based on US FDA approval and US patents and may be different from those in different countries
CTLA-4 cytotoxic T-lymphocyte-associated protein 4, FDA Food and Drug Administration, ICI immune checkpoint inhibitors, PD-L1 programmed death-ligand 1