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This is an investigational vaccine combination consisting of a pentavalent DTaP-HB-PRP~T vaccine and an oral poliovirus vaccine (OPV), developed by Sanofi Pasteur. The pentavalent component is a biologic containing diphtheria toxoid, tetanus toxoid, acellular pertussis antigens (pertussis toxoid and filamentous hemagglutinin), hepatitis B surface antigen, and Haemophilus influenzae type b (Hib) capsular polysaccharide conjugated to tetanus toxoid (PRP~T). It is intended for the active immunization of infants against diphtheria, tetanus, pertussis, hepatitis B, and invasive Hib infections. In clinical trials, it is administered concomitantly with OPV to provide additional protection against poliomyelitis, following the WHO Expanded Programme on Immunization (EPI) schedule. This combination aims to simplify infant vaccination schedules by reducing the number of injections while maintaining immunogenicity comparable to established whole-cell pertussis-based pentavalent vaccines.
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