Evaluating the Safety and Immunogenicity of pDNA Vaccines Expressing HIV M Group p24^Gag Conserved Elements and/or p55^Gag, Administered With IL-12 pDNA by Intramuscular Electroporation, in Healthy, HIV-Uninfected Adults

This study will evaluate the safety, tolerability, and immunogenicity of two HIV-1 pDNA
vaccines: p24CE1/2 pDNA and p55^gag pDNA administered with IL-12 pDNA adjuvant, given by
intramuscular (IM) injection with electroporation (EP), in healthy, HIV-uninfected adults.

Participants will be randomly assigned to one of four groups: Group 1 Treatment, Group 1
Control, Group 2 Treatment, or Group 2 Control.

Participants in Group 1 Treatment will receive p24CE1/2 pDNA and IL-12 pDNA at Day 0 and
Month 1, then p24CE1/2 pDNA plus p55^gag pDNA and IL-12 pDNA at Months 3 and 6. Participants
in Group 1 Control will receive placebo (sodium chloride for injection) at Day 0 and Months
1, 3, and 6.

Participants in Group 2 Treatment will receive p55^gag pDNA and IL-12 pDNA at Day 0 and
Months 1, 3, and 6. Participants in Group 2 Control will receive placebo (sodium chloride for
injection) at Day 0 and Months 1, 3, and 6.

Study visits will occur at Day 0, Week 2, and Months 1, 1.25, 1.5, 3, 3.5, 6, 6.25, 6.5, 9,
and 12. Visits may include physical examinations and clinical assessments, blood and urine
collection, optional stool collection, HIV testing, risk reduction counseling, and
interviews/questionnaires. At Month 18, study staff will contact participants for follow-up
health monitoring.

Inclusion Criteria:

General and Demographic Criteria

- Age of 18 to 50 years

- Access to a participating HIV Vaccine Trials Network (HVTN) clinical research site
(CRS) and willingness to be followed for the planned duration of the study

- Agrees not to enroll in another study of an investigational research agent prior to
completion of last required protocol visit (excludes annual health contact visit)

- Good general health as shown by medical history, physical exam, and screening
laboratory tests

HIV-Related Criteria:

- Assessed by the clinic staff as being at "low risk" for HIV infection and committed to
maintaining behavior consistent with low risk of HIV exposure through the last
required protocol clinic visit.

Laboratory Inclusion Values

- Hemoglobin greater than or equal to 11.0 g/dL for volunteers who were born female,
greater than or equal to 13.0 g/dL for volunteers who were born male

- White blood cell count equal to 3,300 to 12,000 cells/mm^3

- Total lymphocyte count greater than or equal to 800 cells/mm^3

- Remaining differential either within institutional normal range or with site physician
approval

- Platelets equal to 125,000 to 550,000/mm^3

- Chemistry panel: alanine aminotransferase (ALT), aspartate aminotransferase (AST), and
alkaline phosphatase less than 1.25 times the institutional upper limit of normal;
creatine phosphokinase (CPK) less than or equal to 2.0 times the institutional upper
limit of normal; creatinine less than or equal to institutional upper limit of normal.

Virology

- Negative HIV-1 and -2 blood test: U.S. volunteers must have a negative Food and Drug
Administration (FDA)-approved enzyme immunoassay (EIA).

- Negative Hepatitis B surface antigen (HBsAg)

- Negative anti-Hepatitis C virus antibodies (anti-HCV), or negative HCV polymerase
chain reaction (PCR) if the anti-HCV is positive

- Normal urine:

- Negative urine glucose, and

- Negative or trace urine protein, and

- Negative or trace urine hemoglobin

Reproductive Status

- Reproductive status: A volunteer who was born female must:

- Agree to consistently use effective contraception for sexual activity that could
lead to pregnancy from at least 21 days prior to enrollment through the last
required protocol clinic visit.

- Or not be of reproductive potential, such as having reached menopause (no menses
for 1 year) or having undergone hysterectomy, bilateral oophorectomy, or tubal
ligation;

- Or be sexually abstinent.

Exclusion Criteria:

General

- Allergy to amide-type local anesthetics (bupivacaine [Marcaine], lidocaine
[Xylocaine], mepivacaine [Polocaine/Carbocaine], etidocaine [Duranest], prilocaine
[Citanest, EMLA® cream])

- Investigational research agents received within 30 days before first vaccination

- Body mass index (BMI) greater than or equal to 40; or BMI greater than or equal to 35
with 2 or more of the following: age greater than 45, systolic blood pressure greater
than 140 mm Hg, diastolic blood pressure greater than 90 mm Hg, current smoker, known
hyperlipidemia

- Intent to participate in another study of an investigational research agent or any
other study that requires non-HVTN HIV antibody testing during the planned duration of
the study

- Pregnant or breastfeeding

- Active duty and reserve U.S. military personnel

Vaccines and other Injections

- HIV vaccine(s) received in a prior HIV vaccine trial. For volunteers who have received
control/placebo in an HIV vaccine trial, the HVTN Protocol Safety Review Team (PSRT)
will determine eligibility on a case-by-case basis.

- Previous receipt of monoclonal antibodies (mAbs), whether licensed or investigational;
the HVTN 119 PSRT will determine eligibility on a case-by-case basis.

- Non-HIV experimental vaccine(s) received within the last 5 years in a prior vaccine
trial.

Immune System

- Immunosuppressive medications received within 168 days before first vaccination.

- Serious adverse reactions to vaccines or to vaccine components

- Autoimmune disease

- Immunodeficiency

Clinically significant medical conditions

- Untreated or incompletely treated syphilis infection

- Clinically significant medical condition, physical examination findings, clinically
significant abnormal laboratory results, or past medical history with clinically
significant implications for current health.

- Any medical, psychiatric, occupational, or other condition that, in the judgment of
the investigator, would interfere with, or serve as a contraindication to, protocol
adherence, assessment of safety or reactogenicity, or a volunteer's ability to give
informed consent

- Psychiatric condition that precludes compliance with the protocol. Specifically
excluded are persons with psychoses within the past 3 years, ongoing risk for suicide,
or history of suicide attempt or gesture within the past 3 years.

- Current anti-tuberculosis (TB) prophylaxis or therapy

- Asthma exclusion criteria: Asthma other than mild, well-controlled asthma.

- Diabetes mellitus type 1 or type 2, including cases controlled with diet alone. (Not
excluded: history of isolated gestational diabetes.)

- Thyroidectomy, or thyroid disease requiring medication during the last 12 months

- Hypertension

- Bleeding disorder diagnosed by a doctor (e.g., factor deficiency, coagulopathy, or
platelet disorder requiring special precautions)

- Malignancy

- Seizure disorder

- Asplenia

- History of hereditary angioedema, acquired angioedema, or idiopathic angioedema.

- Presence of implanted electronic medical device (e.g., cochlear implant, pacemaker,
implantable cardioverter defibrillator)

- Presence of surgical or traumatic metal implant at the intended site of administration
(including the deltoid muscles and/or overlying skin)

- Sinus bradycardia (defined as less than 50 beats per minute (bpm) on exam) or a
history of cardiac arrhythmia: e.g., supraventricular tachycardia, atrial
fibrillation, or frequent ectopy. NOTE: Sinus arrhythmia is not excluded.