FDA authorized monoclonal antibodies for treatment of COVID-19

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On Nov. 21, 2020, the FDA issued an emergency use authorization (EUA) for Regeneron Pharmaceuticals’ casirivimab and imdevimab to be administered together for treatment of mild to moderate COVID-19 in adults and pediatric patients with positive results of direct SARS-CoV-2 viral testing and who are at high risk for progressing to severe COVID-19.

This included those who are 65 years of age or older or who have certain chronic medical conditions.

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Source: U.S. Food and Drug Administration
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