CTRI/2017/07/009038进行中（未招募）3 期
Randomized, Multi-centric, Open-label, Comparator-controlled Study to evaluate the efficacy and safety of RABIMABs administered in conjunction with Vaxirab N for Post-exposure Prophylaxis in Patients following Potential Rabies Exposure
试验速览
- 阶段
- 3 期
- 状态
- 进行中（未招募）
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.Male and Female patients aged 5 years or more than 5 years.
- •2.WHO Category III exposure(s) by a suspected rabid animal.
- •3.Have documented informed consent from individuals, the childâ??s parent(s) or legal guardian(s) and assent from the child if appropriate.
- •4.Free of obvious health problems as determined by history and examination.
- •5.If female, not pregnant or lactating at the time of enrolment and not planning pregnancy during the vaccination period.
- •6.Male subjects must be agree to use at least one effective contraceptive method throughout the entire duration of the study.
排除标准
- •1.Pregnant and lactating women.
- •2.Patient has received any dose of rabies vaccines / rabies immunoglobulin in the past.
- •3.Allergic to any of the vaccine component / human rabies immunoglobulin components.
- •4.Chronic administration of immunosuppressants or other immune-modifying agents.
- •5.Unable to follow all required study procedures for the whole period of the study.
- •6.Acute febrile illness or acute infectious disease.
研究者
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