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21 December 2021 | By Hannah Balfour (European Pharmaceutical Review)
The EMA has recommended granting marketing authorisation for the use of Xevudy (sotrovimab) to treat COVID-19 in adults and adolescents.
2 December 2021 | By Anna Begley (European Pharmaceutical Review)
The Medicines and Healthcare products Regulatory Agency (MHRA) approve sotrovimab for people with mild to moderate COVID-19 infection and at least one risk factor for developing severe illness.
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