JPRN-jRCT2080221032未知2 期
A Multi-center, Randomized, Single-blind, Dose-Ranging Study to Evaluate Immunogenicity, Safety and Tolerability of Different Doses of Adjuvanted Cell-Derived, Inactivated Novel Swine Origin A/H1N1 Monovalent Subunit Influenza Virus Vaccine in Healthy Japanese Pediatric Subjects
ovartis Pharma K.K.0 个研究点目标入组 120 人开始时间: 2010年3月2日最近更新:
试验速览
- 阶段
- 2 期
- 发起方
- 入组人数
- 120
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
- >= 至 <= 19age old(—)
- 性别
- All
入选标准
- •Healthy Japanese aged 6 months to 19 years
排除标准
- •- History of anaphylaxis, serious vaccine reactions, hypersensitivity to vaccine viral proteins or excipients
- •- Administration of adjuvanted influenza vaccine or suspected influenza disease within 3 month prior to study start
- •- Administration of any other vaccines within 4 weeks prior to enrollment expect for seasonal influenza vaccines within 1 week
- •- History of progressive or severe neurological disorders
研究者
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A Multi-center, Randomized, Single-blind, Dose-Ranging Study to Evaluate Immunogenicity, Safety and Tolerability of Different Doses of Adjuvanted Cell-Derived, Inactivated Novel Swine Origin A/H1N1 Monovalent Subunit Influenza Virus Vaccine in Healthy Japanese Adult SubjectsJPRN-jRCT2080221031ovartis Pharma K.K.200
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