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    Home > Medical News > Latest Medical News > Deck Pharma announces that the Phase Ib clinical trial application of ATG-008 combined with ATG-010 has been approved in China

    Deck Pharma announces that the Phase Ib clinical trial application of ATG-008 combined with ATG-010 has been approved in China

    • Last Update: 2021-11-14
    • Source: Internet
    • Author: User
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    Shanghai and Hong Kong November 2, 2021/PRNewswire/ - Deqi Pharmaceutical Co.
    , Ltd.
    , a leading innovative biopharmaceutical company dedicated to the development and commercialization of the first of its kind and/or best-in-class hematology and oncology therapies ( Abbreviated as "Deqi Pharmaceutical", Hong Kong Stock Exchange stock code: 6996.
    HK) today announced that the National Medical Products Administration (NMPA) has approved ATG-008 (onatasertib) in combination with ATG-010 (selinexor) for the treatment of relapsed/refractory An open phase Ib study on the dose exploration and safety of diffuse large B-cell lymphoma (rrDLBCL)
    .

    The trial is in China with Sun Yat-sen University Cancer Center as the lead research center, and it is planned to be carried out in 10 domestic research centers
    .
    The study is divided into a dose exploration phase and a dose expansion phase.


    The enrolled subjects with relapsed/refractory diffuse large B-cell lymphoma will receive the combination therapy of ATG-008 and ATG-010


    ATG-008 is a potent and selective inhibitor of mammalian target of rapamycin (mTOR) kinase, which simultaneously inhibits mTORC1 and mTORC2
    .
    ATG-008 inhibits cell growth and induces apoptosis in multiple hematoma cell lines, including 23 DLBCL cell lines


    .


    Professor Cai Qingqing, a professor at Sun Yat-sen University Affiliated Tumor Hospital, doctoral supervisor, and head of the Lymphoma Group of the Oncology Branch of the Guangdong Medical Association, said: “DLBCL is one of the most common types of non-Hodgkin’s lymphoma, about 30- 40% of patients will experience relapse or refractory
    .
    Patients with relapse and refractory have a poor prognosis and limited treatment options


    .


    Dr.


    Mei Jianming, founder, chairman and CEO of Deqi Pharmaceuticals, said: “I am very pleased that the National Medical Products Administration has approved ATG-008 combined with ATG-010 in the treatment of rrDLBCL for the dose exploration and safety of the open phase Ib clinical study.


    About the MATCH test

    The trial is a dose-exploring, open phase Ib clinical study aimed at treating adult patients with relapsed/refractory diffuse large B-cell lymphoma (rrDLBCL) with ATG-008 (onatasertib) combined with ATG-010 (selinexor) Perform dose exploration and safety assessment


    .


    About Deqi Pharmaceutical

    Deqi Pharmaceutical Co.
    , Ltd.
    (abbreviated as "Deqi Pharmaceutical", Hong Kong Stock Exchange stock code: 6996.
    HK) is a leading R&D-driven biopharmaceutical company dedicated to providing the most advanced therapies and treatments for patients in Asia Pacific and even the world Tumors and other life-threatening diseases
    .
    Since its official operation in 2017, Deqi Pharmaceuticals has established a rich product pipeline that extends from pre-clinical to clinical stages through cooperative introduction and independent research and development


    .


    Forward-looking statements

    The forward-looking statements made in this article only relate to events or information as of the date when the statement is made in this article
    .
    Except as required by law, we have no obligation to update or publicly revise any forward-looking statements and unexpected events after the date of forward-looking statements, regardless of whether new information, future events or other circumstances appear


    .


    Source: Deqi Pharmaceutical Co.


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