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临床试验/NCT01335347
NCT01335347已完成1 期

A Dose Escalation Phase 1 Safety and Immunogenicity Study of an Oral Viral Vector Vaccine Encoding Avian Influenza H5N1 Hemagglutinin Protein and dsRNA Adjuvant in Healthy Adults

Vaxart1 个研究点 分布在 1 个国家目标入组 54 人开始时间: 2011年4月最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
发起方
Vaxart
入组人数
54
试验地点
1
主要终点
Frequency or severity of vaccine related events as measured through reported AEs

研究概览

简要总结

The purpose of this study is to demonstrate the safety and immunogenicity of an oral vaccine to prevent avian influenza. Volunteers will receive either one or two doses of research vaccine or placebo as part of this study.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 49 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • In good health as established by medical history, physical examination and laboratory testing at the time of enrollment.

排除标准

  • Has had any other vaccines within the past 8 weeks.
  • Has had prior H5 avian influenza investigational vaccine.
  • Current history of chronic alcohol consumption and/or illicit and/or recreational drug use.
  • History of autoimmune related disease.
  • History of any confirmed or suspected immunodeficient or immunosuppressive condition (no congenital or acquired condition that impedes normal immune response, no concurrent immunosuppressive therapy).
  • Positive serology for HIV, HCV, or HBV.
  • Previous serious reactions to vaccination such as anaphylaxis, respiratory problems, hives or abdominal pain.
  • History of irritable bowel disease or other inflammatory digestive or gastrointestinal conditions that could affect the intended distribution or safety evaluation of an orally administered vaccine targeting the mucosa of the small intestine.
  • Use of proton pump inhibitors (Nexium, Prilosec) that substantially increases stomach pH.
  • Stool sample with occult blood at baseline exam

结局指标

主要结局

Frequency or severity of vaccine related events as measured through reported AEs

时间窗: up to 1 year

次要结局

  • Magnitude of humoral immune responses to avian influenza as measured by functional assays(up to 1 year)
  • Magnitude of cellular immune responses to avian influenza as measured by functional assays(up to 1 year)

研究者

发起方
Vaxart
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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