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Eli Lilly's third COVID-19 neutralizing antibody receives FDA emergency use authorization for Omicron

 Last Update: 2022-05-29
 Source: Internet
 Author: User

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Recently, Eli Lilly announced that its new crown neutralizing antibody bebtelovimab has been granted Emergency Use Authorization (EUA) by the FDA for the treatment of patients with mild to moderate new coronary pneumonia

Bebtelovimab, a broad-spectrum neutralizing antibody introduced by Eli Lilly from Abcellera, has potent neutralizing activity against all currently known mutant strains, including the "Omicron" strain

The authorization is based on data from a Phase II clinical BLAZE-4 trial (NCT04634409)

Not long ago, Eli Lilly had signed an order with the U.

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