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The trivalent subunit influenza vaccine is a seasonal prophylactic vaccine designed to protect against three strains of the influenza virus. Unlike whole-virus or split-virion vaccines, subunit vaccines contain only highly purified viral surface proteins—specifically hemagglutinin (HA) and neuraminidase (NA)—which are the primary targets for neutralizing antibodies. This purification process is intended to minimize the presence of internal viral proteins and host-cell contaminants, potentially leading to a better safety profile and lower reactogenicity. The specific candidate mentioned in the context is being developed by Beijing Baihui Biotechnology and Bohui Biopharmaceutical. It is currently in Phase I clinical trials in China (CTR20254002), where it is being evaluated for safety and immunogenicity in a population aged 3 years and older using both single and two-dose immunization schedules.
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