CTRI/2018/01/011500已完成4 期
An open label study for Collection of Human Blood Sample for Development of Anti-Vi IgG testing standard, in process of developing a new Conjugate Vaccine for Typhoid Enteric fever caused by Salmonella Typhi - None
Biological ELimited0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
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
入选标准
- •1. Provide voluntary written and signed informed consent from volunteer.
- •2. Healthy subjects aged 18 to 30 years of both gender.
- •3. Are not participating in or plan to participate in another research during the next three months & be available throughout study period.
- •4. Family does not plan to move during the study period, and housed not further that 50 KM away from the study site.
排除标准
- •1. Fever of any origin or infections more than 3 days within one month prior
- •to screening or on the day of screening
- •2. Any confirmed or suspected immunosuppressive condition.
- •3. Use of any marketed or investigational or herbal medicine or non-registered drug or vaccine for typhoid.
- •4. In receipt of systemic immunosuppressant or systemic corticosteroids.
- •5. Prior or anticipated receipt of immune globulin or other blood products, or other immune modulator therapy.
- •6. Life threatening or serious cardiac, respiratory, gastrointestinal, hepatic, renal, endocrine and systemic disorders.
- •7. Have been vaccinated against typhoid fever or had exposure to typhoid fever within the last three years.
- •8. Suspected or known hypersensitivity to any of the investigational or marketed vaccine components.
- •9. Any condition that, in the opinion of the investigator, would pose a health risk to the participant, or interfere with the evaluation of the study objectives.
研究者
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