跳至主要内容
临床试验/NCT00350623
NCT00350623终止2 期

A Phase IIa Dose-Refinement Study of the Safety and Immunogenicity of a 3-Dose Regimen of the Merck Adenovirus Serotype 5 HIV-1 Gag/Pol/Nef Vaccine in Healthy Adults

Merck Sharp & Dohme LLC0 个研究点目标入组 210 人开始时间: 2006年10月最近更新:
适应症

试验速览

阶段
2 期
状态
终止
入组人数
210
主要终点
Number of Enzyme-linked Immunosorbent Spot (ELISPOT) Responders at 30 Weeks

研究概览

简要总结

This study will test the safety and immunogenicity of an investigational Human Immunodeficiency Virus (HIV) vaccine. Immunogenicity will be measured by evaluating the immune response to several different dose levels.

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
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Demonstrates good general health
  • Human Immunodeficiency Virus (HIV), Hepatitis B surface Antigen (HBsAg), and Hepatitis C (HCV) seronegative
  • Low risk of acquiring HIV infection
  • ALT lab value within normal range

排除标准

  • Previously received an investigational HIV vaccine
  • Has a known or suspected impairment of immunologic function
  • Has a clinically significant chronic medical condition that is considered progressive
  • Has a major psychiatric illness
  • Has any history of malignancy, with the exception of basal cell or squamous cell skin cancer
  • Weighs less than 105 lbs.
  • Has a recent (within two years) history of chronic alcohol abuse
  • Has a contraindication to intramuscular (IM) injection, such as anticoagulant therapy or thrombocytopenia
  • Female is pregnant or breast feeding, or expecting to conceive or donate eggs during the study
  • Male subject is planning to impregnate or provide sperm donation during the study

结局指标

主要结局

Number of Enzyme-linked Immunosorbent Spot (ELISPOT) Responders at 30 Weeks

时间窗: 30 weeks

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

相似试验