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FLU-Q-PAN H7N9 Formulation 1 + AS03B is a **combination vaccine** composed of an inactivated, split-virion monovalent Influenza A (H7N9) virus antigen (typically manufactured via propagation in embryonated hen’s eggs and subsequent inactivation and purification) together with the **AS03B adjuvant** (an oil-in-water emulsion containing squalene, DL-α-tocopherol, and polysorbate 80). This adjuvanted influenza vaccine is designed to improve immunogenicity against avian influenza A (H7N9) and is generally supplied as separate vials to be mixed immediately prior to use. The **mechanism of action** is induction of protective humoral immune responses (notably hemagglutination-inhibition antibodies) against the H7N9 virus, with AS03B enhancing the magnitude and breadth of this response. Clinical data support the use of adjuvanted H7N9 influenza vaccines to achieve greater immune responses than unadjuvanted comparators, particularly in pandemic preparedness scenarios due to the poor immunogenicity of unadjuvanted H7N9 vaccines[2]. Developers and manufacturers commonly include GSK (for the AS03B adjuvant) and Sanofi Pasteur (for the H7N9 antigen)[2].
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