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    Home > Medical News > Medicines Company News > Innovent Biologics PD-1/IL-2 bispecific antibody fusion protein IBI363 completed the first clinical patient administration in Australia

    Innovent Biologics PD-1/IL-2 bispecific antibody fusion protein IBI363 completed the first clinical patient administration in Australia

    • Last Update: 2022-09-24
    • Source: Internet
    • Author: User
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    Cinda Biopharmaceutical Group (HKEx Stock Code: 01801), a biopharmaceutical company dedicated to the research and development, production and sales of innovative drugs in the field of oncology, self-immunity, metabolism, ophthalmology and other major diseases, Today announced the completion of its self-developed recombinant anti-programmed death receptor 1 (PD-1) antibody fusion interleukin 2 (IL-2) bispecific molecule (R&D code: IBI363) in a Phase I clinical trial in Australia for the treatment of advanced solid tumors or


    The study (NCT05290597) was an open-label, multicenter phase I study whose primary objective was to evaluate the safety, tolerability, and initial efficacy of IBI363 in subjects with advanced solid tumors or lymphomas, and to determine the phase II recommended dose (RP2D).


    Interleukin-2 (IL-2) is a cytokine secreted by CD4+ T cells mainly activated by antigens, which plays an important role


    IBI363 is a potential First-in-Class new drug independently developed by Innovent Biologics, with the active ingredient of PD-1/IL-2 bispecific antibody fusion protein


    Dr.


    Dr.


    Cinda Biopharmaceutical Group (HKEx Stock Code: 01801), a biopharmaceutical company dedicated to the research and development, production and sales of innovative drugs in the field of oncology, self-immunity, metabolism, ophthalmology and other major diseases, Today announced the completion of its self-developed recombinant anti-programmed death receptor 1 (PD-1) antibody fusion interleukin 2 (IL-2) bispecific molecule (R&D code: IBI363) in a Phase I clinical trial in Australia for the treatment of advanced solid tumors or


    The study (NCT05290597) was an open-label, multicenter phase I study whose primary objective was to evaluate the safety, tolerability, and initial efficacy of IBI363 in subjects with advanced solid tumors or lymphomas, and to determine the phase II recommended dose (RP2D).


    Interleukin-2 (IL-2) is a cytokine secreted by CD4+ T cells mainly activated by antigens, which plays an important role


    IBI363 is a potential First-in-Class new drug independently developed by Innovent Biologics, with the active ingredient of PD-1/IL-2 bispecific antibody fusion protein


    Dr.


    Dr.


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