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Britain’s GSK said the deal brought the total number of doses secured of the treatment, branded Xevudy, to more than 750,000 globally, adding that the United States would have an option to buy additional doses through March 2022.
The companies did not specify how many doses the U.S. government had signed up for.
The U.S. Food and Drug Administration in May gave an emergency use authorization https://www.reuters.com/business/healthcare-pharmaceuticals/us-fda-gives-emergency-use-approval-gsk-vir-covid-19-antibody-drug-2021-05-26 to the GSK-Vir treatment for treating mild-to-moderate COVID-19 in people aged 12 years and older, who are at the risk of their illness worsening.
