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This recombinant human papillomavirus bivalent vaccine targets types 16 and 18 of the Human Papillomavirus. It is designed to evaluate its safety and immunogenicity in healthy females aged 9-45 years. The vaccine is administered via a three-dose schedule (0, 2, 6 months) and aims to induce an immune response, specifically neutralizing antibodies, against HPV types 16 and 18. The recombinant proteins are produced in yeast.
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