HIV Infections
Conditions
Keywords
IL-12, IL-15, HIV Seronegativity, HIV Preventive Vaccine
Brief summary
The purpose of this study is to determine the safety of and immune response to an experimental HIV vaccine, HIV-1 gag DNA, with and without an IL-15 DNA adjuvant (at escalating doses of 100, 500, and 1500 mcg). This study will also test the safety of and immune response to the HIV-1 gag DNA vaccine plus IL-15 DNA adjuvant given with or without 2 other adjuvant-containing booster vaccines.
Detailed description
The HIV epidemic is a major global health challenge, causing tremendous human suffering and economic loss throughout the world. The need for a safe, effective, and affordable HIV preventive vaccine is critical. This 2-part study will determine the safety and immunogenicity of the experimental HIV vaccine HIV-1 gag DNA with or without IL-15 adjuvant, boosted with either the HIV-1 gag DNA and IL-15 adjuvant vaccine or the HIV-1 gag DNA and IL-12 adjuvant vaccine. There are two parts to this study. Part A will last 12 months. In Part A, 48 participants will be randomly assigned to 1 of 4 groups in sequential order (dose escalation). All participants will receive 3 vaccinations. Group 1 will receive 3 vaccinations of the HIV-1 gag DNA vaccine or placebo. Group 2 will receive 3 vaccinations of either the HIV-1 gag DNA vaccine with a low dose of IL-15 adjuvant or a placebo. Group 3 will receive 3 vaccinations of either the HIV-1 gag vaccine with a medium dose of IL-15 adjuvant or a placebo. Group 4 will receive 3 vaccinations of either the HIV-1 gag vaccine with a high dose of IL-15 adjuvant or a placebo. Vaccinations will be given at Months 0, 1, and 3. There will be 11 study visits in Part A. A physical exam, pregnancy prevention counseling, medication history, and adverse event reporting will occur at most visits. Urine and blood collection will occur at some visits. Participants will also be asked to complete questionnaires at certain visits. Part B will last 15 months. In Part B, 72 participants will be randomly assigned to 1 of 2 groups. All Part B participants will receive 5 vaccinations. Group 5 will receive 5 vaccinations of either the HIV-1 gag vaccine plus IL-15 DNA or placebo; the vaccinations will occur at Months 0, 1, 3, 6, and 9. Group 7 will receive 3 vaccinations of the HIV-1 gag vaccine with a high dose of IL-15 adjuvant (maximum tolerated dose from Part A) followed by 2 vaccinations of the gag DNA vaccine with IL-12 DNA adjuvant. Some participants will receive placebo instead of this vaccine regimen. For Group 7, the HIV-1 gag vaccine with IL-15 adjuvant vaccinations will be given at Months 0, 1, and 3, and booster vaccinations will be given at Months 6 and 9. There will be 13 study visits in Part B. A physical exam, pregnancy prevention counseling, medication history, and adverse event reporting will occur at most visits. Urine and blood collection will occur at some visits. Participants will also be asked to complete questionnaires at certain visits.
Interventions
BIOLOGICALHIV-1 gag DNA
DNA vaccine containing the HIV gene gag
BIOLOGICALIL-15 DNA adjuvant
Cytokine injection
BIOLOGICALIL-12 DNA adjuvant
Cytokine injection
Sponsors
National Institute of Allergy and Infectious Diseases (NIAID)
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
DOUBLE (Subject, Caregiver)
Eligibility
Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes
Inclusion criteria
Note: Group 6 has been removed from Part B of the protocol as of the 04/11/06 amendment. Because a regimen similar to Group 6's regimen is being tested in HVTN 060, the vaccine manufacturer decided that Group 6's regimen was not a priority for testing. Inclusion Criteria: * HIV uninfected * Access to a participating HIV Vaccine Trials Unit (HVTU) * Willing to receive HIV test results * Willing and able to comply with all study requirements * In good general health * Willing to use acceptable methods of contraception for at least 21 days prior to study entry and until the last study visit. More information about this criterion can be found in the protocol. * Hepatitis B surface antigen negative * Anti-hepatitis C virus (anti-HCV) antibody negative or negative HCV PCR if anti-HCV antibody is positive
Exclusion criteria
* HIV vaccines in prior HIV vaccine trial * Immunosuppressive medications within 168 days prior to first vaccination * Blood products within 120 days prior to first vaccination * Immunoglobulin within 60 days prior to first vaccination * Live attenuated vaccines within 30 days prior to first vaccination * Investigational research agents within 30 days prior to first vaccination * Medically indicated subunit or killed vaccines within 14 days prior to first study vaccine administration, or allergy treatment with antigen injections within 30 days prior to first vaccination * Current tuberculosis (TB) prophylaxis or therapy * Clinically significant medical condition, physical exam findings, abnormal laboratory results, or past medical history with clinically significant implications for current health * Any medical, psychiatric, or social condition that, in the opinion of the investigator, may interfere with the study * Any occupational or other responsibility that, in the opinion of the investigator, may interfere with the study * Diagnosis of allergy to amide-type local anesthetics * Serious adverse reaction to vaccines, including anaphylaxis and related symptoms such as hives, respiratory difficulty, angioedema, or abdominal pain. A person who had an adverse reaction to pertussis vaccine as a child is not excluded. * Autoimmune disease or immunodeficiency * Unstable asthma * Diabetes mellitus Type 1 or Type 2. Participants with histories of isolated gestational diabetes are not excluded. * Thyroid disease requiring treatment in the past 12 months * Serious angioedema within the last 3 years * Uncontrolled hypertension * Body mass index (BMI) of 40 or greater OR BMI of 35 or greater, when certain other criteria are met. More information about these criteria can be found in the protocol. * Bleeding disorder * Cancer. Participants with surgically removed cancer that, in the opinion of the investigator, is unlikely to recur are not excluded. * Seizure disorder requiring medication within the past 3 years * Absence of the spleen * Psychiatric condition, including psychoses within the past 3 years, ongoing risk for suicide, or history of suicide attempt or gesture within the past 3 years * Pregnant or breastfeeding, or plan to become pregnant during the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Local and systemic reactogenicity signs and symptoms, as assessed after each injection | 12 months postinjection for Part A, and 15 months after the first injection in Part B |
| Laboratory measures of safety, as assessed after each injection | 12 months postinjection for Part A, and 15 months after the first injection in Part B |
| Adverse and serious adverse experiences, as assessed after each injection | 12 months postinjection for Part A, and 15 months after the first injection in Part B |
Secondary
| Measure | Time frame |
|---|---|
| HIV-specific cellular responses by IFN-gamma ELISpot | 12 months postinjection for Part A, and 15 months after the first injection in Part B |
| HIV binding antibody by ELISA | 12 months postinjection for Part A, and 15 months after the first injection in Part B |
| Social impact variables | At the end of the study |
Countries
Brazil, United States
Outcome results
None listed