PACTR202307828402450尚未招募3 期
The Impact of a combination of the RTS,S/AS01E Malaria Vaccibe and Perennial Malaria Chemoprevention in Ghanaian Children
适应症
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 发起方
- PATH
- 入组人数
- 2,310
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
- 1 Month(s) 至 23 Month(s)（—）
- 性别
- All
入选标准
- •1. Provision of a signed and dated informed consent form by a parent or guardian.
- •2. A statement by the parent or guardian of a willingness to comply with all study procedures and of their availability for the duration of the study.
- •3. Aged 14 - 18 weeks at enrollment.
- •4. The infant is in good general health as evidenced by their medical history and by a physical examination.
- •5. The infant is able to take oral medication.
排除标准
- •1. Current use of a disallowed concomitant medications.
- •2. Current participation in another intervention trial.
- •3. Prior administration of a malaria vaccine.
- •4. Known allergic reactions to components of SP, AQ or to RTSS/AS01 E .
- •5. Any other condition(s) or diagnosis, or physical examination finding that precludes participation
- •as assessed by a study clinician.
研究者
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