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    Home > Medical News > Latest Medical News > 5 COVID-19 drugs included in the EU priority accelerated review: 4 antibodies and 1 JAK inhibitor

    5 COVID-19 drugs included in the EU priority accelerated review: 4 antibodies and 1 JAK inhibitor

    • Last Update: 2021-08-29
    • Source: Internet
    • Author: User
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    In the fight against epidemic variants, the European Union has identified five COVID-19 treatment drugs, which will be reviewed on a priority basis, and it is hoped that three of them will be approved by October


    Specifically, the EU has selected 4 monoclonal antibody programs, including: Eli Lilly antibody cocktail bamlanivimab/etesevimab, Celltrion regdanvimab, Roche/regeneron antibody cocktail casirivimab/imdevimab, Vir/GSK sotrovimab


    Also selected was Eli Lilly’s oral JAK inhibitor Olumiant (baricitinib), a drug that has been approved for the treatment of rheumatoid arthritis and atopic dermatitis


    This work aims to provide greater regulatory flexibility through rolling reviews, conditional marketing authorizations, and flexible labeling and packaging requirements


    To this end, the EU will hold an industry "blind date conference" on July 12th and 13th


    An obvious leader is the antibody cocktail therapy from Regeneron


    Eli Lilly’s antibody cocktail bamlanivimab/etesevimab is the first drug approved in the United States to treat patients at high risk of developing severe COVID-19


    GSK/Vir’s sotrovimab antibody was licensed for use in the United States last month, but the two companies have not yet reached a supply agreement with the U.


    In October last year, Europe purchased 500,000 doses of Gilead’s antiviral drug Remdesivir for US$1.


    In a statement, the EU said: “The EU hopes to add more promising treatments to this investment portfolio in the fight against COVID-19, reaching 10 by the end of the year, but this will depend on the results of research and development


    Reference source: Regeneron, GlaxoSmithKline and Eli Lilly COVID-19 drugs prioritized for expedited review in Europe

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