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临床试验/NCT00545987
NCT00545987已完成1 期

Evaluation of Local and Systemic Reactogenicity Following Serial Administration of ADVAX, a Clade C DNA Vaccine, ADVAX e/g + ADVAX p/N-t, by Ichor TriGrid™ in Vivo Electroporation to HIV-Uninfected, Healthy Volunteers

Rockefeller University1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2007年9月1日最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
已完成
入组人数
40
试验地点
1
主要终点
To evaluate the safety of an intramuscular prime and boost injection of the ADVAX DNA-based HIV vaccine via TriGrid™ electroporation at all three dosing levels

研究概览

简要总结

This study will test the safety of a HIV DNA vaccine after it is injected into your muscle using an electroporation device (TriGrid™ Delivery System made by Ichor Medical Systems), and will test the ability of the vaccine to help your body make antibodies and T-Cells.

In this study, we would like to learn about the effects that electroporation of the HIV DNA has on you and your immune system.

详细描述

Over 40 million people worldwide are currently infected with HIV, the virus that causes AIDS (Acquired Immune Deficiency Syndrome). The number of new cases continues to rise at an alarming rate. Other infectious diseases, such as smallpox or poliomyelitis, have been controlled, or even eliminated, by vaccination programs. Many experts believe that an HIV vaccine offers the best hope for controlling the epidemic.

Many different possible HIV vaccines are currently being developed and tested.

The ADVAX vaccine which you will receive is one vaccine that has been tested. To date, one to three doses of the ADVAX vaccine have been given to 45 individuals in a study that took place between December 2003 and October 2005 at the Rockefeller University and the University of Rochester and it appears to be safe. The difference between this ADVAX study and the previous one is that you will only receive two doses of the vaccine or placebo by either standard intramuscular injection or by "electroporation."

This study is part of a broader research effort to see if changes in the way vaccines are given can make vaccines more effective.

The results of other studies suggest that using regular needles may not be the most potent way to inject this type of vaccine. This is why we are studying a new method of injection called electroporation.

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
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Healthy Men and Women
  • •Ages 18 to 60
  • •Not considered to be at high risk to acquire HIV infection.

排除标准

  • •Confirmed HIV-1 or HIV-2 infection
  • •Any clinically significant abnormality on history or examination
  • •Any clinically significant acute or chronic medical condition requiring care of a physician (e.g., diabetes, coronary artery disease, rheumatologic illness, malignancy, substance abuse) that in the opinion of the investigator would preclude participation
  • •Hepatitis B; hepatitis C
  • •If female, pregnant, planning a pregnancy during the trial period, or breastfeeding
  • •Receipt of a live attenuated vaccine (other than influenza) within 30 days or other vaccine within 14 days of ADVAX vaccination
  • •Receipt of blood transfusion or blood products 6 months prior to vaccination
  • •Participation in another clinical study of an investigational product currently or within past 3 months, or expected participation while enrolled in this study
  • •History of severe local or systemic reactogenicity to vaccination or history of severe allergic reactions
  • •Major psychiatric illness including any history of schizophrenia or severe psychosis, bipolar disorder requiring therapy, suicidal attempt or ideation in the previous 3 years
  • •Any electronic stimulation device, such as cardiac demand pacemakers, automatic implantable cardiac defibrillator, nerve stimulators, or deep brain stimulators
  • •Individuals in which a skin-fold measurement of the cutaneous and subcutaneous tissue for all eligible injection sites (deltoid muscles with intact lymph drainage) exceeds 40 mm
  • •In the opinion of the investigator, unlikely to comply with protocol

研究组 & 干预措施

intramuscular injection

Active Comparator

administration of an HIV-1 vaccine by conventional intramuscular injection

干预措施: conventional intramuscular injection (Device)

TriGrid Delivery System

Experimental

electroporation-mediated intramuscular delivery using the TriGridTM device by Ichor Medical Systems, Inc.

干预措施: TriGrid™ Delivery System (Device)

结局指标

主要结局

To evaluate the safety of an intramuscular prime and boost injection of the ADVAX DNA-based HIV vaccine via TriGrid™ electroporation at all three dosing levels

时间窗: wk. 1,2, 4, 9, 10, 12, 16, 24, 36, 48 and 56

次要结局

  • • To evaluate the immunogenicity of an intramuscular prime and boost injection of the ADVAX DNA-based HIV vaccine via TriGrid™ electroporation compared to placebo or standard syringe injection at all three dosing levels.(wk. 1,2, 4, 9, 10, 12, 16, 24, 36, 48 and 56)

研究者

申办方类型
Other

研究点 (1)

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