Safety and Effectiveness of PENNVAX-B Vaccine Alone, With Il-12, or IL-15 in Healthy Adults

National Institute of Allergy and Infectious Diseases (NIAID)

Status and phase: Completed; Phase 1

Conditions: HIV Infections

Treatments: Biological: PennVax B; Biological: IL-15; Biological: IL-12

Study type: Interventional

Funder types: NETWORK; NIH

Identifiers

NCT00528489

HVTN 070

10490 (Registry Identifier)

Details and patient eligibility

About

The purpose of this study is to determine the safety, tolerability, and immune response to the DNA HIV vaccine, PENNVAX-B alone, in combination with IL-12, or with 2 different doses of IL-15.

Full description

A vaccine that is effective against multiple strains of HIV remains the best option for preventing the spread of HIV. Plasmid DNA vaccines are inexpensive and easy to construct. When DNA vaccines are administered in combination with cytokines, such as IL-12 or IL-15, the immune response to the vaccine is increased. The purpose of this study is to determine the safety and tolerability of the DNA plasmid vaccine, PENNVAX-B when administered alone, or with IL-12 or IL-15 DNA adjuvants. The most effective and safe dose of IL-15 will also be determined during this study.

This study will last approximately 12 months. Participants will be randomly assigned to one of four groups. Group 1 will receive an injection of PENNVAX-B combined with 0.8 mg IL-15 in each deltoid or placebo. Group 2 will receive an injection of PENNVAX-B alone or placebo. Group 3 will receive an injection of PENNVAX-B combined with IL-12 in each deltoid or placebo. Group 4 will receive PENNVAX-B combined with 2 mg IL-15 or placebo. Injections will occur at study entry, Months 1, 3, and 6. Additional study visits will occur on Days 14, 42, 98, 182, 273, and 364. At these visits a brief physical, blood collection, interview, and risk reduction counseling will occur. At some visits HIV testing, urine collection, and pregnancy tests will also occur.

As of 05/30/08, participants will be enrolled into Groups 3 and 4 at a limited pace to allow for additional safety reviews for the first few participants in these groups. Additionally, safety data will be reviewed for Groups 1 and 2 to determine whether the remainder of participants in Groups 2, 3, and 4 will be enrolled.

Enrollment: 120 patients

Sex: All

Ages: 18 to 50 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• HIV-1 and -2 uninfected
• Willing to receive HIV test results
• Good general health
• Certain laboratory values within normal range or with site physician approval
• Negative for Hepatitis B surface antigen
• Negative Hepatitis C test
• Willing to use acceptable methods of contraception

Exclusion criteria

• HIV vaccines or placebos in prior HIV trial. Participants who can provide documentation that they received a placebo in a prior HIV trial may be eligible.
• Immunosuppressive medications within 168 days prior to first study vaccination. Participants using corticosteroid nasal spray for allergies or topical corticosteroids for mild, uncomplicated dermatitis are not excluded.
• Blood products within 120 days prior to first study vaccination
• Receipt of immunoglobulin within 60 days prior to first vaccination
• Live attenuated vaccines within 30 days prior to first study vaccination
• Any vaccine that is not a live attenuated vaccine within 14 days prior to first study vaccination
• Investigational research agents within 60 days prior to first study vaccination
• Current anti-tuberculosis (TB) preventive therapy or treatment clinically significant medical condition, abnormal physical exam findings, abnormal laboratory results, or past medical history that may affect current health. More information about this criterion can be found in the protocol.
• Any medical, psychiatric, social, occupational, or other condition or responsibility that in the opinion of the investigator would interfere with the study. More information about this criterion can be found in the protocol.
• Allergy to amide-type local anesthetics
• Serious adverse reactions to vaccines
• Autoimmune disease or immunodeficiency
• Active syphilis infection. Participants who have been fully treated for syphilis over 6 months prior to study entry are not excluded.
• Asthma other than mild, well-controlled asthma. More information on this criterion can be found in the protocol.
• Type 1 or type 2 diabetes mellitus. Participants with histories of isolated gestational diabetes are not excluded.
• Thyroidectomy or thyroid disease requiring medication during the 12 months prior to study entry
• Accumulation of fluid in the blood vessels (angioedema) within 3 years prior to study entry if episodes are considered serious or have required medication in the 2 years prior to study entry
• Uncontrolled hypertension
• Body Mass Index of 40 or greater OR of 35 or greater if certain other criteria apply. More information about these criteria can be found in the protocol
• Bleeding disorder
• Cancer. Participants with surgically removed cancer that is unlikely to recur are not excluded.
• Seizure disorder
• Absence of the spleen
• Pregnancy or breastfeeding

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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120 participants in 4 patient groups

1

Experimental group

Description:

PENNVAX-B with 0.8 mg IL-15 administered in both deltoids at Months 0, 1, 3, and 6

Treatment:

Biological: IL-15

Biological: PennVax B

2

Experimental group

Description:

PENNVAX-B administered alone in both deltoids at Months 0, 1, 3, and 6

Treatment:

Biological: PennVax B

3

Experimental group

Description:

PENNVAX-B administered alone in both deltoids at Months 0, 1, 3, and 6

Treatment:

Biological: IL-12

Biological: PennVax B

4

Experimental group

Description:

PENNVAX-B with 2 mg IL-15 injected into both deltoids at Months 0, 1, 3, and 6

Treatment:

Biological: IL-15

Biological: PennVax B