Alphamab Oncology announced that its Investigational New Drug $(IND)$ application for JSKN027, an independently developed PD-L1/VEGFR2 bispecific antibody-drug conjugate, has been officially accepted by the Center for Drug Evaluation $(CDE)$ of the National Medical Products Administration of China. The company plans to initiate a phase I clinical study to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and preliminary anti-tumor activity of JSKN027 in patients with advanced malignant solid tumors.
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