AZD7442 request for emergency use authorisation for COVID-19 prophylaxis filed in US

AstraZeneca

5 October 2021 - Filing includes data from PROVENT Phase 3 trial showing 77% reduction in risk of developing symptomatic COVID-19 with long-acting antibody combination (non-vaccine).

AstraZeneca has submitted a request to the US FDA for an emergency use authorisation for AZD7442, its long-acting antibody combination, for prophylaxis of symptomatic COVID-19.

Read AstraZeneca press release

Michael Wonder

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Michael Wonder

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Medicine , US , COVID-19