PACTR201008000221638Other未知
Safety and immunogenicity of a heterologous prime-bosst vaccine strategy with AdCh63 ME-TRAP and MVA ME-TRAP in healthy adults, children and infants in a malaria endemic area
Oxford University, Jenner Institute0 个研究点目标入组 52 人开始时间: 2010年6月15日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- Other
- 发起方
- 入组人数
- 52
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
- 2 Year(s) 至 50 Year(s)(—)
- 性别
- Male
入选标准
- •Consenting adult males and children aged 2-6 years in good health
排除标准
- •Any of the following constitute an exclusion criterion:
- •¿Clinically significant history of skin disorder (psoriasis, contact dermatitis etc.), allergy, symptomatic immunodeficiency, cardiovascular disease, respiratory disease, endocrine disorder, liver disease, renal disease, gastrointestinal disease, neurological illness.
- •¿History of allergic disease or reactions likely to be exacerbated by any component of the vaccine, e.g. egg products, Kathon.
- •¿History of splenectomy.
- •¿Haemoglobin less than 9.0 g/dL
- •¿Serum creatinine concentration above >130mmol/L
- •¿Serum ALT concentration >69 IU/L
- •¿Blood transfusion within one month ofenrolment. .
- •¿History of vaccination with previous experimental malaria vaccines.
- •¿Administration of any other vaccine or immunoglobulin within two weeks before vaccination.
- •¿Current participation in another clinical trial, or within 12 weeks of this study.
- •¿Any other finding which in the opinion of the investigators would increase the risk of an adverse outcome from participation in the trial.
- •¿Likelihood of travel away from the study area.
- •¿HIV positive.
研究者
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