Japan’s ministry of health, labour and welfare issued an emergency use authorization (EUA) on 27 September for GlaxoSmithKline plc/Vir Biotechnology, Inc.’s single-dose monoclonal antibody Xevudy (sotrovimab), for the treatment of patients with mild-to-moderate COVID-19 who do not require supplemental oxygen but are at high risk of progressing to severe disease.
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