AB&B Bio-Tech Receives NMPA Approval for Trivalent Subunit Influenza Vaccine

Reuters01-30
AB&B Bio-Tech Receives NMPA Approval for Trivalent Subunit Influenza Vaccine

AB&B Bio-Tech Co. Ltd. JS announced that its new drug application for a trivalent subunit influenza vaccine has been approved by the National Medical Products Administration (NMPA) of China. This vaccine is the first and only trivalent subunit influenza vaccine approved in China for all age groups at full dosage level as of the date of the announcement. The company states that this product offers comprehensive protection, high antigen purity, and low risks of adverse reactions compared to traditional split-virion vaccines. The announcement notes that there is no assurance the company will ultimately be able to develop and market the vaccine for all intended age groups successfully.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. AB&B Bio-Tech Co. Ltd. JS published the original content used to generate this news brief via IIS, the Issuer Information Service operated by the Hong Kong Stock Exchange (HKex) (Ref. ID: HKEX-EPS-20260130-12005846), on January 30, 2026, and is solely responsible for the information contained therein.

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