Lilly's monoclonal antibody therapy bamlanivimab has been granted Emergency Use Authorization in the US for recently diagnosed, mild-to-moderate COVID-19 in high-risk patients.
The decision by the US Food and Drug Administration makes Lilly the first to bring an antibody therapy to patients, ahead of Regeneron, which submitted its ‘antibody cocktail’ REGN-COV2 on the same day just over a month ago – shortly after President Trump received the treatment
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