CTIS2024-511506-22-00进行中（未招募）1 期
A two-centre open-label non-inferiority trial to assess the immunogenicity and safety of an intradermal and an intramuscular single-visit dosing regimen of purified chick-embryo cell-culture rabies vaccine in adults
Institute Of Tropical Medicine0 个研究点目标入组 360 人开始时间: 2024年2月13日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 360
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
- 年龄范围
- 18 至 64（—）
- 性别
- All
入选标准
- •=18 to =60 years of age at time of inclusion, Willingness to provide written informed consent, Permanent residency in Belgium during the study period, Prepared to follow the study schedule, Willing to use contraception during 1 month after each vaccination (only for women of childbearing potential)
排除标准
- •Any vaccination against rabies (memorised or stated in the vaccination certificate), Known allergy to one of the components of the vaccines, Immunocompromised subjects or subjects who take immunosuppressant and/or –stimulant medication, Planned overseas deployment during the study period, Ongoing pregnancy or active child wish during the study period (for female subjects), Planned vaccination with any inactivated vaccine within 2 weeks before or after each vaccination or with any live attenuated vaccine within 1 month before or after each vaccination
研究者
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