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临床试验/EUCTR2011-005101-79-Outside-EU/EEA
EUCTR2011-005101-79-Outside-EU/EEA进行中(未招募)不适用

Safety and Immunogenicity of a Quadrivalent Influenza VaccineAdministered via the Intramuscular Route in Child/Adolescent and AdultSubjects

Sanofi Pasteur0 个研究点目标入组 2,083 人开始时间: 2012年10月5日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
2,083

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

  • Children/adolescents aged 9 to 17 years (or adults aged 18 to 60 years) on the day of inclusion.
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 382
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 1701
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Previous vaccination against influenza with the 2012 Southern Hemisphere formulation or the 2011–2012 Northern Hemisphere formulation in the previous 6 months with either the trial vaccine or another vaccine.

研究者

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