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A randomized, double-blind and placebo-controlled phase I study to evaluate the safety and immunogenicity of a 9-valent Human Papillomavirus (HPV) vaccine, administered intramuscularly according to a 0, 2, 6-month schedule in 9 to 45 years old healthy Chinese females.
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Interventional model
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90 participants in 2 patient groups, including a placebo group
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Data sourced from clinicaltrials.gov
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