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TARRYTOWN, N.Y., Aug. 20, 2021 /PRNewswire/ — UK chief medical officers to confirm how antibody cocktail will be rolled-out on the National Health Service (NHS) in the coming weeks In the U.S., Regeneron has completed the first FDA BLA submission for the antibody cocktail; more than 130,000 doses were distributed in the past week to address COVID-19 outbreaks Regeneron Pharmaceuticals, Inc. (NASDAQ: REGN) today announced that the United Kingdom’s (UK) Medicines and Healthcare products Regulatory Agency (MHRA) has granted Conditional Marketing Authorization (CMA) for the casirivimab and imdevimab antibody cocktail, known as REGEN-COV™ in the U.S. and Ronapreve® in the UK and other countries, to prevent and treat acute COVID-19 infection.
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