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    Home > Biochemistry News > Biotechnology News > The world's first FRα ADC is expected to submit an FDA Biologics License Application in March

    The world's first FRα ADC is expected to submit an FDA Biologics License Application in March

    • Last Update: 2022-05-22
    • Source: Internet
    • Author: User
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    On March 20, 2022, Huadong Medicine issued an announcement stating that ImmunoGen, a wholly-owned subsidiary of the company’s Sino-US Huadong-US partner, announced that its organization developed a new class 1 biological drug for the treatment of ovarian cancer, Mirvetuximab Soravtansine (IMGN853, referred to as "" Mirvetuximab") full study results of the US pivotal single-arm clinical trial ("SORAYA trial"): the trial has met the primary endpoint, with a confirmed objective response rate (ORR) of 32.


    ImmunoGen expects to file a Biologics License Application (BLA) for Mirvetuximab in the United States this month


    Huadong Medicine stated that Mirvetuximab is the world's first FRα-targeted ADC drug and is a key product under development in the company's innovative oncology drug pipeline


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