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)
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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