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. 2023 Jan 11;12(1):5. doi: 10.3390/antib12010005

Table 3.

List of antibodies that received authorization for COVID-19 treatment up to November 2022.

No Antibodies Name Current Status References
1 Bebtelovimab Remain authorized in the U.S. until further notice by the FDA. [30,83]
2 Tixagevimab with
cilgavimab
Remain authorized with the recommendation of repeat dosing every six months with a dose of 300 mg of tixagevimab and 300 mg of
Cilgavimab.
[84,85]
3 Sotrovimab Since 5 April 2022, no longer
authorized in any U.S. region; approved in Australia, the UK, and the EU.
[86,87,88]
4 Bamlanivimab with etesevimab Pausing all distribution. [81,89]
5 Casirivimab with imdevimab Currently not authorized in any U.S. region; however, it is recommended to be retained for future SARS-CoV-2 variants that may be susceptible. [33,88,90]
6 Amubarvimab/romlusevimab Approved in China. [88]
7 Regdanvimab (CT-P59) Approved in the Republic of Korea and the EU. [88]
8 Ronapreve Approved in Japan, the UK, the EU, and Australia. [88]
9 F61 Approved for clinical trials in China. [91]
10 Tocilizumab Authorized for emergency use in June 2021. [92,93]
11 Sarilumab Clinical trial phase 3. [94]
12 Adalimumab Clinical trial phase 3. [95]
13 Canakinumab Clinical trial phase 3. [96]
14 Ravulizumab Completed clinical phase 3; recruiting phase 4 trials. [97,98]
15 Lenzilumab Clinical trial phase 3. [99]

Abbreviation: EUA, emergency use authorization; FDA, U.S. Food and Drug Administration; mg, milligram.