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临床试验/NCT00973700
NCT00973700已完成3 期

A Randomized, Open Label, Single Center, Dose- and Regimen-Ranging Study to Evaluate Immunogenicity, Safety and Tolerability of Different Formulations of an Adjuvanted and Non-Adjuvanted Egg-Derived, Inactivated Novel Swine Origin A/H1N1 Monovalent Subunit Influenza Virus Vaccine in Healthy Children and Adults Ages 3 to 64 Years

Novartis Vaccines1 个研究点 分布在 1 个国家目标入组 784 人开始时间: 2009年8月最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
784
试验地点
1
主要终点
Percentage of Subjects With Seroconversion and HI Titer ≥1:40 in Children 3 to 17 Years of Age

研究概览

简要总结

This study will evaluate the safety and immunogenicity of different combinations of A/H1N1 S-OIV (swine flu) vaccine in healthy young children, adolescents, and adults.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
3 Years 至 64 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Children, adolescents, and adults 3 to 64 years of age in good health as determined by medical history, physical assessment and clinical judgement of the investigator and without influenza within the past 6 months.

排除标准

  • History of serious disease.
  • History of serious reaction following administration of vaccine or hypersensitivity to vaccine components.
  • Known or suspected impairment/alteration of immune function.
  • Receipt or planned receipt of seasonal trivalent influenza vaccine within 1 week before or after each study vaccination.
  • For additional entry criteria, please refer to protocol.

结局指标

主要结局

Percentage of Subjects With Seroconversion and HI Titer ≥1:40 in Children 3 to 17 Years of Age

时间窗: Day 1 to day 387

Seroconversion: The percentage of subjects with either a pre-vaccination HI titer \< 1:10 and a post-vaccination HI titer \>1:40 or a prevaccination HI titer \>1:10 and a minimum four-fold rise in post-vaccination HI antibody titer. The analyses were performed on the Per-Protocol Set (PPS).

Percentage of Subjects With Seroconversion and HI Titer ≥ 1:40 in Adults 18 to 64 Years of Age

时间窗: Day 1 to day 387

Seroconversion: The percentage of subjects with either a pre-vaccination HI titer \< 1:10 and a post-vaccination HI titer \>1:40 or a prevaccination HI titer \>1:10 and a minimum four-fold rise in post-vaccination HI antibody titer. Analyses were performed on the Per-Protocol set (PPS).

次要结局

  • Percentage of Subjects With Seroconversion and HI Titer ≥1:40, in Adults 18 to 64 Years(7 days and 21 days after each vaccination)
  • Percentage of Subjects With Seroconversion and HI Titer ≥1:40, in 3 to <9 Years and 9 to 17 Years(Day 1 to day 387)
  • HI GMRs, in 3 to <9 Years and 9 to 17 Years(Day 1 to day 387)
  • Number of Subjects With at Least One Reactogenicity Sign, in 18 to 64 Years of Age(7 days after each vaccination)
  • Age Distribution at Baseline(Baseline)
  • HI GMR, in Adults 18 to 64 Years(Day 1 to day 387)
  • Number of Subjects With at Least One Reactogenicity Sign, in 3 to <9 Years of Age(7 days after each vaccination)
  • Number of Subjects With at Least One Reactogenicity Sign, in 9 to 17 Years of Age(7 days after each vaccination)

研究者

发起方
Novartis Vaccines
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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