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临床试验/PACTR201008000221638
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

发起方
Oxford University, Jenner Institute

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