Monoclonal antibody therapy for prevention of severe disease in nosocomial COVID-19
Background: In November 2020, the FDA issued an emergency use authorization (EUA) for monoclonal antibodies (mAbs) to be used in outpatients with COVID-19 infections who are at a high risk of progressing to severe disease. However, becuase the EUA had limited indications for inpatients, data on thei...
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Cambridge University Press,
2022-07-01T00:00:00Z.
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