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临床试验/JPRN-jRCT2080222050
JPRN-jRCT2080222050已完成1 期

A randomized, double-blind, comparative study of VN-100 in healthy adult Japanese volunteers

DAIICHISANKYO Co.,Ltd.0 个研究点目标入组 600 人开始时间: 2013年3月27日最近更新:

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
600

研究概览

简要总结

As a result of the immunogenicity and safety of VN-100 in healthy adults and elderly, a good increase in antibody titer and safety were confirmed. The immunogenicity of VN-100 with 6 micro g, 9 micro g, and 15 micro g was similar to subcutaneous influenza HA vaccine.

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 20age old 至 ot applicable(—)
性别
All

入选标准

  • Healthy adult Japanese volunteers

排除标准

  • 1) Subjects with history of seasonal influenza in the past 6 months
  • 2) Subjects with history of seasonal influenza vaccination in the past 6 months

研究者

发起方
DAIICHISANKYO Co.,Ltd.

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