FDA grants emergency use authorization for COVID-19 drug

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FDA grants emergency use authorization for COVID-19 drug
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Chloe Nordquist is a national journalist for the E.W. Scripps Company. She has a passion for telling community stories and giving a voice to the voiceless. Chloe has had the opportunity to report across the world, as far as Milan and Berlin. Previously she worked at news stations in California’s Central Valley and Southwest Florida.

Pemgarda, made by Invivyd, is an infusion drug made for those who are immunocompromised to help support the immune system in preventing COVID-19 infection.

The FDA wrote in the announcement that this treatment is authorized for those who “have moderate-to-severe immune compromise due to a medical condition or due to taking immunosuppressive medications or treatments and are unlikely to mount an adequate immune response to COVID-19 vaccination.” @scrippsnewsQualified individuals can get the monoclonal antibody infusion once every three months at most.

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