The Medical Letter on Drugs and Therapeutics
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1614
December 28, 2020
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Issue 1614
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An EUA for Casirivimab and Imdevimab for COVID-19
December 28, 2020 (Issue: 1614)
The FDA has issued an Emergency Use Authorization (EUA) for Regeneron's investigational monoclonal antibodies casirivimab and imdevimab (REGEN-COV) to be administered together by IV infusion or SC injection for treatment of mild to moderate...more
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