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临床试验/ISRCTN33950739
ISRCTN33950739已完成不适用

Assessment of the humoral immune response and safety of reduced doses of influenza vaccine administered intradermally compared to intramuscular administratio

Berna Biotech AG, Crucell Company (Switzerland)0 个研究点目标入组 275 人开始时间: 2007年11月14日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
275

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • Healthy volunteers between 18 and 60 years of age.

排除标准

  • 1. Pregnancy and lactation
  • 2. Treatment with immunoglobulins or blood transfusions
  • 3. Immunodeficiency
  • 4. History of egg protein allergy/severe atopy/serious adverse reaction to influenza vaccine
  • 5. Previous vaccination against influenza in the past 330 days
  • 6. Participation in another clinical trial
  • 7. Known blood coagulation disorders
  • 8. Acute febrile illness

研究者

发起方
Berna Biotech AG, Crucell Company (Switzerland)

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