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Marketing Application for Quadrivalent Influenza Virus Subunit Vaccine for Children Aged 6-35 Months Accepted!
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- Time of issue:2024-06-28
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(Summary description)On June 28, 2024, Ab&B Bio Tech Co., Ltd. (hereinafter referred to as "Ab&B Bio") submitted a marketing application for its "quadrivalent influenza virus subunit vaccine" for children aged 6-35 months, which was accepted by the Center for Drug Evaluation (CDE) of the National Medical Products Administration (NMPA) of China.
Marketing Application for Quadrivalent Influenza Virus Subunit Vaccine for Children Aged 6-35 Months Accepted!
(Summary description)On June 28, 2024, Ab&B Bio Tech Co., Ltd. (hereinafter referred to as "Ab&B Bio") submitted a marketing application for its "quadrivalent influenza virus subunit vaccine" for children aged 6-35 months, which was accepted by the Center for Drug Evaluation (CDE) of the National Medical Products Administration (NMPA) of China.
- Categories:Company news
- Author:
- Origin:
- Time of issue:2024-06-28 10:17
- Views:
On June 28, 2024, Ab&B Bio Tech Co., Ltd. (hereinafter referred to as "Ab&B Bio") submitted a marketing application for its "quadrivalent influenza virus subunit vaccine" for children aged 6-35 months, which was accepted by the Center for Drug Evaluation (CDE) of the National Medical Products Administration (NMPA) of China.

Source: Center for Drug Evaluation of the National Medical Products Administration
At present, the influenza virus remains one of the most important respiratory pathogens threatening public health. Seasonal influenza outbreaks or occasional cross-species transmission and pandemics of the influenza virus have significant impacts on human health and socioeconomic development. Especially for infants, the elderly, and patients with underlying cardiovascular and pulmonary diseases, infection with the influenza virus may lead to serious complications such as pneumonia, potentially resulting in severe illness or death. Currently, getting vaccinated against influenza is the most effective measure to prevent influenza infection and pandemics.
The acceptance of this marketing application for the quadrivalent influenza virus subunit vaccine for children aged 6-35 months is another significant milestone for Ab&B Bio's subunit influenza vaccine portfolio. The vaccine has completed Phase III clinical trials and met the expected endpoints. This high-quality vaccine, which combines high purity, low adverse effects, good safety, and comprehensive protection, will become China's first universally applicable quadrivalent influenza virus subunit vaccine for all age groups! It is expected to be approved for market launch in 2025! Ab&B Bio will continue to work diligently to achieve the launch of multiple products, safeguarding human life and health!
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