PER-120-12已完成未知
A PHASE III CLINICAL TRIAL TO STUDY THE IMMUNOGENICITY, TOLERABILITY, AND MANUFACTURING CONSISTENCY OF V503 (A MULTIVALENT HUMAN PAPILLOMAVIRUS [HPV] L1 VIRUS-LIKE PRTICLE [VLP] VACCINE) IN PREADOLESCENTS AND ADOLESCENTS (9 TO 15 YEAR OLDS) WITH A COMPARISON TO YOUNG WOMEN (16 TO 26 YEAR OLDS)
MERCK SHARP & DOHME PERU S.R.L.,0 个研究点目标入组 110 人开始时间: 2013年4月1日最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 110
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 9 至 26（—）
- 性别
- All
入选标准
- •. SUBJECTS WHO ARE ENROLLED IN PROTOCOL 002 BETWEEN 9 AND 15 YEARS OF AGE AND RECEIVED 3 DOSES OF 9-VALENT HPV L1 VLP VACCINE.
排除标准
- •. SUBJECTS WHO ARE CONCURRENTLY ENROLLED IN CLINICAL STUDIES THAT WOULD INVOLVE OR INTERFERE WITH THE COLLECTION OF GENITAL SPECIMENS.
研究者
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A Phase III Clinical Trial to Study the Immunogenicity, Tolerability, and Manufacturing Consistency of V503 (A Multivalent Human Papillomavirus [HPV] L1 Virus-Like Particle [VLP] Vaccine) in Preadolescents and Adolescents (9 to 15 year olds) with a Comparison to Young Women (16 to 26 year olds)Cervical CancersVulvar CancerVaginal CancerGenital LesionsPAP Test AbnormalitiesHPV InfectionsMedDRA version: 20.1Level: LLTClassification code 10063001Term: Human papilloma virus infectionSystem Organ Class: 100000004862EUCTR2009-011617-25-Outside-EU/EEAMerck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc.