AstraZeneca: the EMA approves the marketing of Evusheld


(CercleFinance.com) – The European Medicines Agency (EMA) announces that its Committee for Medicinal Products for Human Use (CHMP) has recommended authorizing the marketing of Evusheld, a treatment combining two monoclonal antibodies, for prevention of COVID-19 from 12 years and 40 kilos.

The two antibodies in the treatment are designed to attach to the spike protein of the SARS-CoV-2 virus, preventing the virus from entering cells and then multiplying there.

To reach its conclusion, the CHMP assessed data from a study involving more than 5,000 people.

The data showed that both injections (150 mg of tixagevimab and 150 mg of cilgavimab), reduced the risk of COVID-19 infection by 77%, with a duration of protection of at least six months.

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