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On July 19, the information on the website of the Center for Drug Evaluation (CDE) of the National Medical Products Administration (NMPA) showed that BeiGene’s PD-1 antibody tislelizumab was planned to be included in the priority review on the grounds of priority.
It is reported that the application for the new indication is based on the results of a single-arm, multi-center, open phase 2 clinical trial