The FDA said last week that bebtelovimab, a monoclonal antibody drug given through a vein, is no longer authorized because it is not effective against the leading strains of COVID-19.
Dec. 4, 2022 – The number of medications available to treat COVID-19 continues to get smaller as the coronavirus changes to outsmart treatments. The FDA said last week that bebtelovimab, a monoclonal antibody drug given through a vein, isBebtelovimab, made by Eli Lilly, was the last remaining monoclonal antibody treatment of six that had been authorized for emergency use during the pandemic.
Bebtelovimab is not effective against the current primary coronavirus strains of BQ.1 and BQ.1.1. Combined, the two strains account for about 63% of all cases nationwide, according toThe FDA announcement stated that antiviral treatments, including remdesivir, Paxlovid, and Lagevrio, are all still options for patients at high risk for a severe case of COVID-19.
COVID-19 is on the rise nationwide, with hospitalizations averaging more than 35,000 per day. This is a 26% increase over the past two weeks, according to“Cases, hospitalizations and test positivity are all rising at the national level, suggesting that the relative stability seen this fall could be coming to an end,” thesummarized. “Daily case and death data are subject to fluctuations around Thanksgiving that do not affect other metrics.
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