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    Home > Medical News > Latest Medical News > The first domestic Junshi PD-1/TGFβ double antibody clinical application was accepted

    The first domestic Junshi PD-1/TGFβ double antibody clinical application was accepted

    • Last Update: 2021-03-24
    • Source: Internet
    • Author: User
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    On February 24, the official website of CDE showed that the clinical application for Junshi Bio-JS201 injection was accepted.


    According to the information officially disclosed by Junshi, the PD-1 antibody of JS201 is partly based on teriprizumab.


    Previously, Merck’s PD-L1/TGFβ dual-antibody M7824 showed good efficacy in the subsequent treatment of multiple cancers such as non-small cell lung cancer and cholangiocarcinoma, and received an advance payment of US$340 million from GlaxoSmithKline+37 The introduction of a milestone amount of 100 million US dollars, a number of factors have ignited the enthusiasm for research and development in this field, and many companies have deployed PD-L1/TGFβ dual antibodies; however, in January this year, Merck decided to terminate the project based on phase III clinical data of non-small cell lung cancer.


    At present, for the PD-L1/TGFβ target, domestic Hengrui Pharmaceuticals and Pumis Biologics have entered the clinic, with Hengrui being the fastest, and it is in clinical phase II; the pre-clinical development companies include Chuangsheng Group, Zejing Pharmaceutical, Lijin Biology, Lepu Biology, Hebo Pharmaceutical, Weilizhibo, Changchun Jinsai.


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