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FDA Expands Junshi/Eli Lilly New Crown Neutralizing Antibody Emergency Authorization

 Last Update: 2021-09-28
 Source: Internet
 Author: User

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On September 16, Eli Lilly announced that the US FDA has expanded its new coronavirus neutralizing antibodies bamlanivimab (700mg) and etesevimab (1400mg) emergency use authorization (EUA) in cooperation with Junshi for post-exposure prevention (PEP)

FDA prevents COVID-19 immune infection

This expanded authorization is based on data from BLAZE-2

bamlanivimab (LY-CoV555) was discovered by AbCellera and developed by Eli Lilly.

etesevimab (JS016 or LY-CoV016) is a recombinant fully human monoclonal neutralizing antibody that specifically binds to the receptor binding domain of the spike protein on the surface of SARS-CoV-2 with high affinity, and can effectively block the virus and host cells Binding of the surface receptor ACE2

On June 25, 2021, the U.

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