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临床试验/ACTRN12605000680662
ACTRN12605000680662尚未招募3 期

Safety and Tolerability of the Japanese Encephalitis Vaccine IC51(JE-PIV).

Intercell AG0 个研究点目标入组 600 人开始时间: 2005年10月21日最近更新:
适应症

试验速览

阶段
3 期
状态
尚未招募
发起方
Intercell AG
入组人数
600

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
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 ot stated(—)
性别
All

入选标准

  • Written informed consent obtained prior to study entry.

排除标准

  • Use of any other investigational or non-registered drug or vaccine in addition to the study vaccine during the study period or within 30 days preceding the first dose of study vaccine- History of any previous JE vaccination- Immunodeficiency including post-organ-transplantation or immunosuppressive therapy- A family history of congenital or hereditary immunodeficiency- History of autoimmune disease- Any acute infections within 2 weeks prior to enrollment- Known or suspected HIV Infection- Pregnancy, lactation or unreliable contraception in female subjects.

研究者

发起方
Intercell AG

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