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Deck Pharmaceuticals announced today that the State Food and Drug Administration has approved the application of ATG-019 to start a phase I clinical trial, which aims to evaluate ATG-019 (single agent or combined with niacinER) in advanced solid tumors or non-Hodgkin’s lymphoma in China Safety and tolerability in patients.
As a PAK4/NAMPT dual-target inhibitor with oral bioavailability, ATG-019 exerts anti-tumor effects through energy consumption, DNA repair inhibition, cell cycle arrest and cell proliferation inhibition, and ultimately promotes cell apoptosis.
Deqi Pharmaceuticals has launched a phase I clinical trial (TEACH) of ATG-019 for the treatment of advanced solid tumors and non-Hodgkin's lymphoma in Taiwan, China.