FDA Approves IND Application for SYS6051 in solid tumors
The Board of Directors (the “Board”) of CSPC Pharmaceutical Group Limited (the “Company”, together with its subsidiaries, the “Group”) is pleased to announce that the Investigational New Drug (IND) application for SYS6051 (the “Product”), an antibody-drug conjugate developed by the Group, has been approved by the U.S.Food and Drug Administration (FDA) to conduct clinical trials in the U.S. The Product also obtained approval from the National Medical Products Administration of the People’s Republic of China in April 2026 to conduct clinical trials in China.
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