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临床试验/CTRI/2018/01/011500
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

发起方
Biological ELimited

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