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临床试验/EUCTR2013-001231-51-ES
EUCTR2013-001231-51-ES进行中(未招募)1 期

Efficacy and Immunogenicity Study of Quadrivalent Influenza Vaccine Administered via the Intramuscular Route in Healthy Children Aged 6 to 35 Months

Sanofi Pasteur0 个研究点目标入组 9,000 人开始时间: 2014年4月4日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
9,000

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Healthy children aged 6 to less than 36 months not previously vaccinated against influenza.
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 9000
  • F.1.2 Adults (18-64 years) no
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • ?At risk? children according to the definition from the Advisory Committee on Immunization Practices (ACIP).

研究者

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