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临床试验/EUCTR2011-001976-21-DE
EUCTR2011-001976-21-DE进行中(未招募)不适用

Safety and Immunogenicity of a Quadrivalent Influenza Vaccine Administered via the Intramuscular Route in Adult and Elderly Subjects

Sanofi Pasteur0 个研究点目标入组 1,568 人开始时间: 2011年7月26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
1,568

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 784
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 784

排除标准

  • - Receipt of any vaccine in the 4 weeks preceding trial vaccination or planned receipt of any vaccine in the 3 weeks following trial vaccination
  • - Previous vaccination against influenza with the 2011-2012 Northern Hemisphere vaccine, with either the trial vaccine or another vaccine

研究者

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