The Australian regulator, the Therapeutic Goods Administration, has granted a provisional approval to GlaxoSmithKline plc/Vir Biotechnology, Inc.’s monoclonal antibody, Xevudy (sotrovimab), for the treatment of COVID-19 in adults and adolescents aged 12 years and older who do not require supplemental oxygen but who are at increased risk of progression to hospitalization or death.
Sotrovimab has been granted interim or emergency authorization in a number of jurisdictions including the US, Canada and Singapore, and the European Medicines Agency has issued advice on its
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