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BioWorld - Friday, July 10, 2026
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Home » China accepts NDA of influenza tablet, clears Tepezza biosimilar
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China accepts NDA of influenza tablet, clears Tepezza biosimilar

March 18, 2025
By Marian (YoonJee) Chu
China’s National Medical Products Administration (NMPA) approved the country’s first injectable teprotumumab biosimilar from Innovent Biologics Inc. under the brand name of Sycume (teprotumumab N-01) to treat thyroid eye disease on March 14. The NMPA on March 15 accepted Simcere Pharmaceutical Group Ltd.’s NDA of deunoxavir marboxil (ADC-189) tablets, a product originally developed by Jiaxing Andicon Biotech Co. Ltd. to treat influenza A and B.
BioWorld BioWorld Asia Regulatory Immune Infection Ocular Respiratory Biosimilar Monoclonal antibody Protein Asia-Pacific China BLA NDA NMPA

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