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Eli Lilly gets the Go for its Monoclonal Antibody Cocktail for “mild to moderate” COVID-19

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the staff of the Ridgewood blog

Ridgewood NJ, according to Johns Hopkins Center for Health Security on February 9, the US FDA issued an Emergency Use Authorization (EUA) for Eli Lilly’s monoclonal antibody cocktail of bamlanivimab and etesevimab as a treatment for COVID-19. The EUA specifically authorizes the treatment for “mild to moderate” COVID-19 in adults and pediatric patients aged 12 years and older who are “at high risk for progressing to severe” disease.

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