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FDA Authorizes New Long-Acting, Monoclonal Antibodies for Pre-exposure Prevention of COVID-19 in Certain Individuals

U.S. Food & Drug Administration   |  December 13, 2021

The FDA is working with sponsors of all currently authorized therapeutics to assess the activity against any global SARS-CoV-2 variant(s) of interest and is committed to communicating with the public as we learn more.

The EUA was issued to AstraZeneca.

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Filed under:Drug Updates Tagged with:AstraZenecacilgavimabCOVID-19EvusheldFDAmonoclonal antibodytixagevimabU.S. Food and Drug Administration (FDA)

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