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临床试验/NCT00197158
NCT00197158已完成4 期

Demonstrate the Non-inferiority of Immunogenicity Elicited by GSK Biologicals' Hepatitis B Vaccine, Multidose Engerix™-B to That of Monodose Engerix™-B When Administered According to 0,1,6 Mths Schedule in Healthy Adults Aged ≥ 18 Yrs

GlaxoSmithKline2 个研究点 分布在 1 个国家目标入组 280 人开始时间: 2005年3月最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
入组人数
280
试验地点
2
主要终点
Measurement of antibody concentrations to hepatitis B antigen at Month 7.

研究概览

简要总结

GSK Biologicals' currently licensed multidose hepatitis B vaccine will be compared to the currently licensed monodose hepatitis B vaccine in a population with well documented hepatitis B immunological response to the vaccine (Belgium).

详细描述

Randomized study with two groups. One group will receive GSK's multidose hepatitis B vaccine and the other group will receive GSK's monodose hepatitis B vaccine

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
Single

入排标准

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

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Measurement of antibody concentrations to hepatitis B antigen at Month 7.

次要结局

  • Measurement of antibody concentrations to hepatitis antigen at Months 1,2and6. Occurrence of solicited local symptoms and solicited general symptoms during the 4-day f/u period after vaccination. Occurrence, intensity and relationship to vaccination

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (2)

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