News
Sotrovimab (VIR-7831) receives emergency use authorization from the FDA for treatment of mild-to-moderate COVID-19 in high-risk adults and paediatric patients.- GSK + Vir Biotechnology Inc.,
GlaxoSmithKline plc and Vir Biotechnology, Inc. announced the FDA granted an Emergency Use Authorization (EUA) for sotrovimab (previously VIR-7831), an investigational single-dose monoclonal antibody, for the treatment of mild-to-moderate COVID-19 in adults and paediatric patients (12 years of age and older weighing at least 40 kg) with positive results of direct SARS-CoV-2 viral testing, and who are at high risk for progression to severe COVID-19, including hospitalisation or death.
Adrienne E. Shapiro, M.D., Ph.D., an infectious disease specialist at Fred Hutchinson Cancer Research Center and investigator in the COMET-ICE trial, said: “Monoclonal antibodies like sotrovimab are potentially one of our most effective tools for fighting COVID-19. While preventive measures, including vaccines, can reduce the total number of cases, sotrovimab is an important treatment option for those who become ill with COVID-19 and are at high risk – allowing them to avoid hospitalisation or worse.”.
Condition: Coronavirus/COVID-19 Infection
Type: drug
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