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    Home > Medical News > Medical World News > Suoyuan Biotech's "first-in-class" new drug successfully achieved overseas authorization

    Suoyuan Biotech's "first-in-class" new drug successfully achieved overseas authorization

    • Last Update: 2021-05-02
    • Source: Internet
    • Author: User
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    Source: Guanlan Pharmaceutical

    On April 14, Suoyuan Biopharmaceuticals and Rumpus Therapeutics/Aytu Biopharma signed a global license agreement for the development of DB102 (enzastaurin) for the treatment of vascular Ehlers-Danglos syndrome (vEDS) and other rare genetic diseases.


    vEDS is a rare genetic disease and a severe subtype of Ehlers-Danlos syndrome.


    DB102 was originally developed by Eli Lilly and Company for the first-line treatment of newly diagnosed high-risk diffuse large B-cell lymphoma (DLBCL) and glioblastoma (GBM).


    Note: The original text has been deleted

    ▽ attention [drug Mingkang Germany ] micro-channel public number

    [Medical attention Mingkang Germany ] ] micro-channel public number

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