USFDA study shows Evusheld retains neutralising activity against Omicron: AstraZeneca

Evusheld is the first long-acting antibody to receive emergency use authorisation in the US for pre-exposure prophylaxis of COVID-19, in addition to authorisations in other countries, and the drug firm is now working with regulators on applications for the use of Evusheld in treating COVID-19, he added. The Omicron variant was not in circulation during the Evusheld clinical trials.