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临床试验/NCT00698893
NCT00698893已完成1 期

An Open Study in Healthy Herpes Simplex Virus (HSV)-Positive Adults to Evaluate the Safety of GSK Biologicals' Candidate gD Vaccine, With or Without 3D MPL

GlaxoSmithKline0 个研究点目标入组 16 人开始时间: 1992年5月1日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
16
主要终点
To evaluate the vaccine safety by repeated physical examination and by recording all local and general signs/symptoms

研究概览

简要总结

The purpose of the study is to evaluate the safety and reactogenicity of candidate gD vaccine, with or without MPL, in HSV-seropositive subjects. The immune response elicited in these subjects will also be evaluated.

详细描述

At the time of conduct of this study, the sponsor GlaxoSmithKline was known by its former name SmithKline Beecham

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Between 18 and 40 years of age
  • Seropositive for antibodies against HSV
  • Female volunteers must have been using contraceptives for at least 2 months before the entry and should avoid becoming pregnant for the duration of this study.
  • Good physical condition as established by physical examination and history taking at the time of entry

排除标准

  • Any abnormal laboratory value among the tests performed at screening.
  • History of persistent hepatic, renal, cardiac or respiratory diseases
  • Clinical signs of acute illness at the time of entry into the study.
  • Previous history of asthma or hypersensitivity to drugs.
  • Seropositive for antibodies against the human immunodeficiency virus
  • Pregnancy and lactation.
  • Treatment with corticosteroids or immunomodulating drugs.
  • Simultaneous participation in another clinical trial.
  • Administration of any other vaccine or immunoglobulins during the study period

结局指标

主要结局

To evaluate the vaccine safety by repeated physical examination and by recording all local and general signs/symptoms

时间窗: Throughout the study

Measurement of haematology/biochemical parameters on blood samples

时间窗: Throughout the study

Vaccine reactogenicity by soliciting of local and general signs/symptoms

时间窗: On the day of vaccination and the subsequent 7 days

Vaccine immunogenicity by 6 measurements of anti-HSV antibodies

时间窗: From day 0 to day 45 following vaccination

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

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