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    Home > Active Ingredient News > Blood System > Deqi Pharmaceuticals PAK4/NAMPT dual target inhibitor ATG-019 clinical trial application approved in China

    Deqi Pharmaceuticals PAK4/NAMPT dual target inhibitor ATG-019 clinical trial application approved in China

    • Last Update: 2021-04-19
    • Source: Internet
    • Author: User
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    On April 6, Deqi Pharmaceuticals announced that the National Medical Products Administration (NMPA) has approved the application of ATG-019 to carry out a phase I clinical trial, aiming to evaluate ATG-019 (single agent or combined with niacinER) in advanced solid tumors or advanced solid tumors in China.
    Safety and tolerability in patients with non-Hodgkin's lymphoma.

    It is understood that ATG-019 is an oral bioavailable PAK4 / NAMPT dual target inhibitor, which can exert anti-tumor effects through energy consumption, DNA repair inhibition, cell cycle arrest and cell proliferation inhibition, and ultimately lead to cell metabolism.
    , Has anti-tumor activity on blood and solid tumor cells dependent on PAK4 and NAMPT signaling pathways.

    Studies have found that in murine tumor models, the anti-tumor effect of ATG-019 combined with anti-PD-1 therapy is better than that of anti-PD-1 monotherapy, indicating that this combination therapy has the potential to treat tumors that are resistant to PD-1 dialysis patient.

    Based on the experimental results of the previous anti-tumor animal model, ATG-019 has launched a phase I clinical trial (TEACH) of ATG-019 in the treatment of advanced solid tumors and non-Hodgkin’s lymphoma in Taiwan, China.
    Phase I clinical trials in patients with advanced solid tumors and non-Hodgkin's lymphoma, and plans to further explore the combination of ATG-019 through clinical studies.

    It is worth mentioning that, as the first p21-activated kinase 4 (PAK4) and nicotinamide phosphoribosyltransferase (NAMPT) oral inhibitor of its kind, ATG-019 has been used in multiple Asia-Pacific markets including Greater China, South Korea, Australia, New Zealand and ASEAN countries have obtained exclusive development and commercialization rights.

    The clinical trial application of ATG-019 has been approved by the NMPA, which fully demonstrates the potential of the drug to prevent and treat Chinese patients.

    In the future, I look forward to the launch of the first clinical trial of ATG-019 in mainland China, which will bring a new treatment option for patients with advanced solid tumors and non-Hodgkin's lymphoma.

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