EUCTR2017-001798-18-Outside-EU/EEA进行中（未招募）1 期
Partnership for Research on Ebola VACcinationsP/0307/2021P/0334/2021 - PREVAC
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- Inserm
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •- Informed consent/assent
- •- Age greater than or equal to 1 year
- •- Planned residency in the area of the study site for the next 12 months
- •- Willingness to comply with the protocol requirements
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range: 1400
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 3450
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 50
排除标准
- •- Fever greater than 38º Celsius
- •- History of EVD (self-report)
- •- Pregnancy (a negative urine pregnancy test is required for females of child-bearing potential, i.e., females who have experienced menarche or who are aged 14 years and older)
- •- Positive HIV test for participants less than 18 years of age
- •- Reported current breast-feeding
- •- Prior vaccination against Ebola (self-report)
- •- Any vaccination in the past 28 days or planned within the 28 days after randomization (initial vaccination)
- •- In the judgement of the clinician, any clinically significant acute/chronic condition that would limit the ability of the participant to meet the requirements of the study protocol
研究者
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