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临床试验/NCT01002040
NCT01002040已完成4 期

PCIRN Evaluation of Pandemic H1N12009 Influenza Vaccine in Adults With Human Immunodeficiency Virus Infection

University of British Columbia4 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2010年2月最近更新:
适应症
干预措施

试验速览

阶段
4 期
状态
已完成
入组人数
150
试验地点
4
主要终点
Occurrence of adverse events (AEs) for days 0-6 after each vaccination

研究概览

简要总结

The purpose of this study is to assess the safety and effectiveness (immune response) to a licensed H1N12009 influenza vaccine in HIV-infected adults. The study will enroll 150 adults (ages 20-59 years). Participants will be randomized into 2 groups and will receive either one dose or two doses of a licensed H1N1 vaccine. Study procedures include: medical history, blood samples and completing a memory aid. Participants will be involved in study related procedures for approximately 6 days.

详细描述

During the first wave of the H1N12009 pandemic in Canada, adults with immune deficiency were more likely to die with severe infections than were other Canadians. Of 76 deaths attributed to date to this new virus, 37% occurred in persons with immune system compromise. Adults with human immunodeficiency virus (HIV) infection constitute a significant proportion of the at-risk population with over 56,000 affected individuals. Most such individuals retain some capacity to respond to influenza vaccination. The dosing regimen for the pandemic vaccine will be based on limited studies in the general population, leaving open the question of whether HIV-infected persons can respond satisfactorily to the recommended dosing. Availability of an adjuvanted formulation of the pandemic vaccine may improve responsiveness but two doses may be required for the best possible response. Thus it would be optimal to evaluate the safety and immunogenicity of the pandemic vaccine among the earliest HIV-infected persons to receive it, to inform the subsequent vaccination of others.

The objectives of this study are three-fold:

  1. To evaluate the safety and immunogenicity of H1N12009 influenza vaccine in a convenience sample of adults with HIV infection.
  2. To compare immune responses of subjects randomized to receive either one or two doses of adjuvanted vaccine to identify the optimal regimen.
  3. To complete this evaluation soon after the pandemic vaccine becomes available so as to inform the subsequent use of the vaccine in HIV-infected persons.

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
None

入排标准

年龄范围
20 Years 至 59 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Laboratory-confirmed HIV
  • Written informed consent
  • Adults 20-59 years of age

排除标准

  • Allergies to eggs, thimerosal or gentamicin sulphate
  • Life-threatening reaction to previous Flu vaccine
  • Bleeding disorder
  • Pregnancy
  • Receipt of blood or blood products in past 3 months
  • Chronic illness
  • Previous lab-confirmed H1N12009 infection
  • Receipt of any non-study H1N12009 or Seasonal Influenza vaccine for 2009/10

研究组 & 干预措施

One Dose Influenza vaccine

Active Comparator

Arepanrix H1N1 Influenza vaccine (one dose)

干预措施: Arepanrix (Biological)

Two Doses Influenza vaccine

Active Comparator

Arepanrix H1N1 Influenza vaccine (2 doses, 3 weeks apart)

干预措施: Arepanrix (Biological)

结局指标

主要结局

Occurrence of adverse events (AEs) for days 0-6 after each vaccination

时间窗: Day 7 and Day 21 post vaccination

Occurrence of serious adverse events (SAEs) and other significant health events up to 21 days after each vaccination

时间窗: Day 7 and Day 21 post vaccination

次要结局

  • Immunogenicity: Comparison of baseline and post-immunization antibody titres(Day 21 post vaccination)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

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