Sotrovimab – Emergency use authorization approval
May 26, 2021 - The FDA announced the emergency use authorization (EUA) approval of GlaxoSmithKline (GSK)/Vir Biotechnology’s sotrovimab, for the treatment of mild-to-moderate coronavirus disease 2019 (COVID-19) in adults and pediatric patients (12 years of age and older weighing at least 40 kilograms [about 88 pounds]) with positive results of direct severe acute respiratory symptom coronavirus 2 (SARS-CoV-2) viral testing and who are at high risk for progression to severe COVID-19, including hospitalization or death.
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