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Poliovirus vaccine SSI is an inactivated poliovirus vaccine (IPV) developed by the Statens Serum Institut (SSI) for the prevention of poliomyelitis. It is a trivalent biologic containing formalin-inactivated poliovirus antigens of Type 1 (Brunhilde strain), Type 2 (MEF-1 strain), and Type 3 (Saukett strain). The development program includes a standard full-dose non-adjuvanted formulation (Poliovaccine SSI) and several reduced-dose formulations (1/3, 1/5, and 1/10 of the standard dose) adsorbed to an aluminium hydroxide adjuvant (IPV-Al SSI). These dose-sparing strategies are intended to improve the affordability and availability of IPV in global markets. A Phase 1 first-in-human trial conducted in Denmark evaluated the safety and immunogenicity of these formulations as boosters in adolescents, confirming they are safe and capable of inducing neutralizing antibody responses.
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