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This is an inactivated, split-virion, non-adjuvanted monovalent vaccine developed for the prevention of influenza A (H1N1) virus infection. Developed and evaluated by the Jiangsu Province Centers for Disease Control and Prevention, the vaccine contains 15 μg of hemagglutinin antigen. It was specifically studied in a prospective cohort and stratified controlled clinical trial involving pregnant women in China to assess safety and immunogenicity. The vaccine demonstrated a high seroconversion rate of 90.4% and was found to be safe for both the mothers and fetal growth, with a low adverse event rate. It was part of the public health response in China following the 2009 H1N1 pandemic.
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