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    Home > Active Ingredient News > Antitumor Therapy > Kangfang Bio-PD-1/CTLA-4 was approved to start a global phase 3 clinical trial for the treatment of cervical cancer

    Kangfang Bio-PD-1/CTLA-4 was approved to start a global phase 3 clinical trial for the treatment of cervical cancer

    • Last Update: 2021-05-08
    • Source: Internet
    • Author: User
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    On April 28, Kangfang Bio-Bio announced that it has independently developed the world's first innovative tumor immunotherapy new drug Cadonilimab (PD-1/CTLA-4, R&D code: AK104) plus platinum-containing chemotherapy with or without bevacizumab It has been approved by the National Center for Drug Evaluation (CDE) to carry out a randomized, double-blind, placebo-controlled global phase III clinical study for the first-line treatment of persistent, recurrent or metastatic cervical cancer.

    This is China’s first first-line phase III clinical study of dual immunotherapy for cervical cancer.
    It is also approved by the U.
    Food and Drug Administration (FDA) as an orphan drug for the treatment of cervical cancer at the end of February.
    The product will be obtained in 2021.
    Another important development in China.

    There is currently no approved standard treatment for patients with cervical cancer who have failed chemotherapy with platinum-containing drugs.

    The objective response rate (ORR) of late-line chemotherapy is less than 10%, the progression-free survival time is short, the long-term chemotherapy is poorly tolerated, and the incidence of adverse reactions is high.
    Effective treatment drugs are needed to improve the efficacy and benefit of patients.

    Cadonilimab (AK104) is a new and potential next-generation backbone drug for PD-1/CTLA-4 bispecific tumor immunotherapy independently developed by Kangfang Bio.
    Its main indications include liver cancer, cervical cancer, lung cancer, gastric cancer, and esophageal squamous cell carcinoma.
    And nasopharyngeal carcinoma and so on.

    Preliminary data in the research of cervical cancer, gastric cancer and other tumors show that Cadonilimab is significantly less toxic than the combination therapy of PD-1 and CTLA-4, and has obvious safety and efficacy advantages.

    A few days ago, Kangfang Biosciences has successfully held this global phase III clinical research expert seminar.
    Many experts and scholars from world-renowned gynecological oncology research institutions including China, the United States, the European Union and Australia attended the meeting.

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