Novavax Seeks FDA Emergency Authorization for COVID-19 Vaccine

Novavax Seeks FDA Emergency Authorization for COVID-19 Vaccine
An illustration picture shows vials with COVID-19 Vaccine stickers attached and syringes with the logo of U.S. biotech company Novavax, on Nov. 17, 2020. Justin Tallis/AFP via Getty Images
Updated:

Novavax announced Monday it has formally submitted a request to the U.S Food and Drug Administration (FDA) to grant emergency use authorization (EUA) for its two-dose vaccine, NVX-CoV2373, for people 18 years and older.

If granted, NVX-CoV2373 would become the fourth COVID-19 vaccine to be made available in the United States. Currently available COVID-19 vaccines are the mRNA-based vaccines—one from Pfizer-BioNTech and the other from Moderna—as well as the non-replicating viral vector vaccine from Johnson & Johnson.

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