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FDA Issues Emergency Use Authorization for Regeneron Monoclonal Antibody Cocktail

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FDA Issues Emergency Use Authorization for Regeneron Monoclonal Antibody Cocktail

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The Food and Drug Administration on Saturday issued an emergency use authorization to Regeneron for its covid-19 monoclonal antibody cocktail, which is made up of the antibodies casirivimab and imdevimab, citing a reduction in hospitalizations and emergency room visits in patients in a clinical trial as well as a…

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