跳至主要内容
临床试验/ACTRN12612000709842
ACTRN12612000709842已完成1 期

A randomised controlled trial to evaluate the immune response to an adjuvanted 2012 seasonal trivalent inactivated influenza vaccine in adults

Vaxine Pty Ltd0 个研究点目标入组 200 人开始时间: 2012年7月3日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
200

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Prevention

入排标准

年龄范围
18 Years 至 o limit(—)
性别
All

入选标准

  • Male or female
  • Age 18 years or over
  • Able to provide written informed consent
  • Willing and able to comply with the protocol for the duration of the study.

排除标准

  • History of vaccination with the 2012 seasonal influenza vaccine
  • History of serious vaccine or egg allergy
  • Women of childbearing potential, unless using a reliable and appropriate contraceptive method, specifically oral contraceptive pill, IUD or mechanical barrier device.
  • Pregnant or lactating women.
  • Receipt of another investigational agent within 14 days preceding initiation of treatment.
  • Any other serious medical, social or mental condition which, in the opinion of the investigator, would be detrimental to the subjects or the study.

研究者

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