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    Home > Active Ingredient News > Drugs Articles > Deck Pharma announced that the Phase I clinical trial application of ATG-101 (the first PD-L1/4-1BB double antibody) was approved in Australia for the treatment of solid tumors and non-Hodgkin’s lymphoma

    Deck Pharma announced that the Phase I clinical trial application of ATG-101 (the first PD-L1/4-1BB double antibody) was approved in Australia for the treatment of solid tumors and non-Hodgkin’s lymphoma

    • Last Update: 2021-07-28
    • Source: Internet
    • Author: User
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    Shanghai, China and Hong Kong, July 20, 2021 – A leading biopharmaceutical company dedicated to the development and commercialization of the world’s first and/or best-in-class blood and innovative tumor therapies – Deqi Pharmaceutical Co.


    ATG-101 is an innovative drug developed by Deqi Pharmaceutical’s R&D team and has global rights and interests.



    ATG-101 is a new PD-L1/4-1BB bispecific antibody, which can block the immunosuppressive PD-L1/PD-1 binding and activate the 4-1BB costimulatory signal to activate the anti-tumor immune effect Cells, while enhancing the efficacy of drugs, enhance safety


    "The entry of ATG-101 into the first human trial as scheduled is a key milestone in the development of Deqi Pharmaceuticals, which fully demonstrates our team's ability to promote preclinical research


    About ATG-101

    ATG-101 is a new PD-L1/4-1BB bispecific antibody that is being developed for the treatment of cancer


    About Deqi Pharmaceutical

    Deqi Pharmaceutical Co.


    Forward-looking statement

    The forward-looking statements made in this article only relate to events or information as of the date when the statement is made in this article


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