HIV Infections Clinical Trial
Official title:
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 TriGridâ„¢ in Vivo Electroporation to HIV-Uninfected, Healthy Volunteers
This study will test the safety of a HIV DNA vaccine after it is injected into your muscle
using an electroporation device (TriGridâ„¢ 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.
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.
Electroporation uses a device that injects substances into muscle along with small amounts
of electricity. This device has been used to a limited extent in human subjects and has been
shown to be more effective than regular needles and safe when tested in animals. Devices
similar to this have been used in many studies to deliver chemotherapy directly into
patients' tumors.
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Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention
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