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临床试验/EUCTR2012-005243-25-FR
EUCTR2012-005243-25-FR进行中(未招募)不适用

Immunogenicity and Safety of the Trivalent Influenza Vaccine (Split-Virion, Inactivated), Northern Hemisphere 2013-2014 Formulation (Intradermal Route)

Sanofi Pasteur0 个研究点开始时间: 2014年4月2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)

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

  • - Aged over 18 years on the day of inclusion
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 65
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 65

排除标准

  • - Subject is pregnant, or lactating, or of childbearing potential
  • - Receipt of any vaccine in the 4 weeks preceding the trial vaccination or
  • planned receipt of any vaccine in the 3 weeks following trial vaccination
  • - Vaccination against flu in the previous 12 months if administered in the
  • context of a clinical trial, or in the previous 6 months if administered in
  • the context of a flu vaccination campaign

研究者

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