Safety of and Immune Response to an Investigational HIV-1 Vaccine With or Without Interleukin-12 (IL-12) in HIV-1 Infected Adults

Although highly active antiretroviral therapy (HAART) has greatly reduced HIV
infection-related morbidity and mortality, individual response to therapy can be variable.
Therapeutic vaccination works by augmenting virus-specific immunity and can be given with or
without immunomodulatory agents or adjuvants. In conjunction with HAART, therapeutic
vaccination may be a more effective treatment for the suppression of HIV-1 replication. This
study will examine the safety and efficacy of giving an investigational vaccine with or
without IL-12 in HIV-1 infected adults receiving HAART. This study will also test whether
delivering the vaccine using EP is safe and increases the efficacy of the vaccine.

Participation in this study will last approximately 36 weeks. Participants will be randomly
assigned to one of five cohorts. Cohort 1 will receive the HIV multi-antigen plasmid DNA
(HIV MAG pDNA) vaccine or placebo intramuscularly (IM) in the upper arm followed by EP.
Cohorts 2 through 4 will receive the HIV MAG pDNA vaccine and sequentially increasing doses
of GENEVAX IL-12 pDNA or placebo by IM/EP. Cohort 5 will receive the HIV MAG pDNA vaccine
with the highest dose of IL-12 pDNA or placebo by needle and syringe in the upper arm.

Participants receive two injections at Weeks 0, 4, and 12. Participants will complete a
questionnaire that assesses the acceptability of the vaccine and remain at the clinic 30
minutes for observation after each vaccination. Participants will be contacted by telephone
2 to 3 days post-vaccination to assess vaccination-related signs and/or symptoms. All
participants will be asked to record their temperatures and any symptoms they experience
daily for 4 days following each vaccination on a Vaccination Report Card (VRC). All nonstudy
vaccines or medications should also be recorded on the VRC. Study visits will occur at Weeks
0, 1, 2, 4, 5, 6, 8, 12, 13, 14, 16, 24, and 36. At most visits, participants will undergo a
physical examination. Women of reproductive potential will also undergo pregnancy testing
before receiving injections on Weeks 0, 4, and 12. Blood will be drawn at various time
points to evaluate participants' health and measure immunologic markers, CD4 and CD8 T-cell
counts, and cytokine levels. Blood and plasma will also be stored for future exploratory
studies.

Inclusion Criteria:

- HIV-1 infected

- Stable antiretroviral therapy (ART) for a minimum of 6 consecutive months prior to
study entry and intention to remain on stable ART until study completion

- CD4 T-cell count greater than or equal to 500 cells/mm3 (within 30 days prior to
study entry)

- At least two measurements of HIV-1 RNA levels less than or equal to 200 copies/mL
(first measurement must be performed at least 6 months prior to study entry and
second measurement must be performed between 6 months prior to study entry and at
least 30 days prior to study entry)

- Screening HIV-1 RNA less than 50 copies/mL (within 30 days prior to study entry)

- Hepatitis B surface antigen negative (within 30 days prior to study entry)

- Hepatitis C antibody negative or, if hepatitis C antibody positive, hepatitis C virus
RNA negative (within 30 days prior to study entry)

- Certain laboratory values obtained within 30 days prior to study entry; more
information can be found in the protocol

- Females of reproductive potential must have a negative urine pregnancy test within 3
days prior to study entry

- All study participants participating in sexual activity that could lead to pregnancy
must agree to use at least one of the following forms of birth control for at least
21 days prior to study entry until the final study visit:

- Condoms (male or female) with or without a spermicidal agent

- Diaphragm or cervical cap with spermicide

- Intrauterine device (IUD)

- Hormone-based contraceptive

- Females who are not of reproductive potential are eligible without requiring the use
of a contraceptive

- Ability and willingness of subject to provide written informed consent

- Collection of a pre-entry PBMC specimen for immunologic assays and entered into the
Laboratory Data Management System (LDMS)

Exclusion Criteria:

- Confirmed (defined as two consecutive values) CD4 T-cell count less than 200
cells/mm3 at any time or any history or subject recollection of CD4 T-cell count less
than 200 cells/mm3 prior to screening

- Any active malignancy that may require chemotherapy or radiation therapy

- Bleeding diathesis or condition associated with prolonged bleeding time that would
contraindicate IM injection

- A skin-fold measurement of the cutaneous and subcutaneous tissue for eligible
injection sites (on the medial deltoid muscles) that exceeds 40 mm

- Use of immunomodulatory, cytokine, or growth stimulating factors such as systemic
corticosteroids, cyclosporine, methotrexate, azathioprine, anti-CD25 antibody,
granulocyte macrophage colony-stimulating factor (GM-CSF), chondrocyte
colony-stimulating factor (C-CSF), IFN, or interleukin-2 (IL-2) (within 30 days prior
to study entry)

- Pregnancy or breastfeeding

- Use of any prior HIV vaccine (prophylactic and/or therapeutic) within 1 year before
study entry

- Use of any investigational treatment within 6 months before study entry

- Use of any licensed or experimental non-HIV vaccination (e.g., hepatitis B,
influenza, pneumococcal polysaccharide) within 4 weeks prior to study entry

- Use of any infusion blood product or immune globulin within 3 months prior to study
entry

- Known or suspected hypersensitivity to any vaccine component, including
hypersensitivity to amide-type local anesthetics, such as lidocaine (Xylocaine),
mepivacaine (Polocaine/Carbocaine), etidocaine (Duranest), bupivacaine (Marcaine), or
prilocaine

- Active drug or alcohol use or dependence that, in the opinion of the site
investigator, would interfere with adherence to study requirements

- Serious illness requiring systemic treatment and/or hospitalization within 7 days
prior to study entry

- Current use of any electronic stimulation device, such as cardiac demand pacemakers,
automatic implantable cardiac defibrillators, nerve stimulators, or deep brain
stimulators

- History of cardiac arrhythmia or palpitations (e.g., supraventricular tachycardia,
atrial fibrillation, frequent ectopy, or sinus bradycardia [i.e., <50 beats per
minute on exam]) prior to study entry (NOTE: Sinus arrhythmia is not excluded)

- History of syncope or fainting episode within 1 year of study entry

- Seizure disorder or any history of prior seizure

- Extensive tattoos covering the site of administration (upper left and right medial
deltoid muscles)

- Presence of any surgical or traumatic metal implants at the site of administration
(medial deltoid muscles)

- Any chronic inflammatory disease (e.g., ankylosing spondylitis, psoriasis,
inflammatory bowel disease)