FDA authorises additional monoclonal antibody for treatment of COVID-19

FDA

26 May 2021 - Today, the U.S. FDA issued an emergency use authorisation for the investigational monoclonal antibody therapy sotrovimab 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. 

This includes, for example, individuals who are 65 years of age and older or individuals who have certain medical conditions.

Read FDA press release

Michael Wonder

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Michael Wonder

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Outcome , Medicine , US , COVID-19