The US Food and Drug Administration has moved to limit the use of GlaxoSmithKline plc/Vir Biotechnology, Inc.’s Xevudy (sotrovimab) in places where SARS-CoV-2 variants resistant to the antibody are spreading.
In an updated fact sheet issued 23 February, the agency said the drug “is not authorized for treatment of mild-to-moderate COVID-19 in geographic regions where infection is likely to have been caused by a non-susceptible SARS-CoV-2 variant based on available
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