The Food and Drug Administration (FDA) has granted emergency use authorization (EUA) for Novavax's COVID-19 vaccine, Covovax.
Covovax is a protein subunit vaccine, meaning it replicates a pure portion of the virus's antigenic part to elicit an immune response.
The vaccine is approved for individuals aged 18 and above and is administered in two doses with a three to four-week interval.
Clinical trials showed Covovax has a very mild adverse event profile and an efficacy rate of approximately 89.7% in preventing COVID-19.
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