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Safety of an HIV DNA Vaccine Given to HIV Uninfected Adults

Primary Purpose

HIV Infections

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
pGA2/JS2 Plasmid DNA Vaccine
Sponsored by
National Institute of Allergy and Infectious Diseases (NIAID)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional prevention trial for HIV Infections focused on measuring Injections, Intramuscular, HIV Seronegativity, Plasmids, Vaccines, DNA, HIV Preventive Vaccine

Eligibility Criteria

18 Years - 40 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria Participants may be eligible for this study if they: Are between the ages of 18 and 40. Are at low risk of HIV infection. Have access to a participating study site and are available for follow-up for 12 months. Complete a questionnaire to evaluate understanding of the study prior to enrollment. Are willing to receive HIV test results. Are in good general health. Do not have hepatitis B. Are HCV antibody negative or, if HCV antibody positive, are HCV PCR negative. Have had a negative HIV blood test within 8 weeks prior to enrollment. Women of childbearing potential must agree to use acceptable methods of contraception. Note: All inclusion criteria must be assessed within 56 days prior to study entry. Exclusion Criteria Participants may not be eligible for this study if they: Have been immunized against smallpox. Have received HIV vaccines or placebo in a previous HIV vaccine trial. Have used drugs that interfere with the immune system within the past 6 months. Have received blood products within 120 days before HIV screening. Have received immunoglobulin within 60 days before HIV screening. Have received a live vaccine within 30 days prior to initial study vaccine administration. Have used investigational research agents within 30 days prior to initial study vaccine administration. Have received a killed vaccine or allergy treatment injections within 14 days of study vaccine administration. Are currently taking anti-TB therapy. Have a history of serious harmful reactions to vaccines. Have a history of immune system disease. Have a history of unstable asthma. Have a history of type I or type II diabetes. Have a history of thyroid disease. Have a history of tissue swelling with serious episodes. Have a history of high blood pressure. Have a history of a bleeding disorder that was diagnosed by a doctor. Have active syphilis. Have a history of cancer, unless it has been surgically removed and in the opinion of the investigator is not likely to recur during the study period. Have a history of a seizure disorder. Have had their spleen removed. Have mental illness that would interfere with compliance with the protocol. Have any other conditions that, in the judgement of the investigator, would interfere with the study. Are pregnant or breast-feeding. Note: All exclusion criteria must be assessed within 56 days prior to study entry.

Sites / Locations

  • Alabama Vaccine CRS
  • UCSF, Gen. Clinical Research Ctr., Mt. Zion Hosp.
  • San Francisco Vaccine and Prevention CRS
  • FHCRC/UW Vaccine CRS

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
August 9, 2002
Last Updated
October 13, 2021
Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
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1. Study Identification

Unique Protocol Identification Number
NCT00043511
Brief Title
Safety of an HIV DNA Vaccine Given to HIV Uninfected Adults
Official Title
A Phase I Trial to Evaluate the Safety and Immunogenicity of the HIV-1 pGA2/JS2 Plasmid DNA Vaccine Given Intramuscularly (IM) in HIV-1 Uninfected Adults
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Completed
Study Start Date
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Primary Completion Date
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Study Completion Date
April 2003 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to see if the experimental HIV vaccine pGA2/JS2 is safe and is well tolerated at two different doses. Another important purpose of this study is to observe how the immune system responds to the vaccine at different dose levels. Vaccines are given to people to help their bodies fight infection. The vaccine being tested in this study is a DNA vaccine. The pGA2/JS2 plasmid DNA vaccine instructs the body to make some HIV proteins. These HIV proteins may trigger an immune response. Because only a few of the many proteins HIV needs are made through DNA vaccination, there is no risk of getting HIV from the vaccination. This and other similar DNA vaccines have been tested for safety in mice, rabbits, and monkeys. The vaccine has been well tolerated at doses to be used in this study.
Detailed Description
DNA vaccination has induced immune responses in animals to a number of viral, bacterial, and parasite derived antigens. Early clinical experiences with HIV DNA vaccines in humans indicate: 1) the tolerability and short-term safety of DNA at doses up to 5000 mcg in humans are excellent; and 2) there is potential for immunogenicity. The pGA2/JS2 DNA vaccine is part of a planned prime/boost regimen of a DNA vaccine prime followed by a modified vaccinia Ankara (MVA) vaccine boost. In studies in monkeys, a combination of a DNA vaccine and an MVA vaccine protected the monkeys against disease caused by a monkey virus similar to HIV. The current study is an initial investigation of the safety and immunogenicity of the DNA vaccine given alone. The pGA2/JS2 DNA vaccine expresses gag, protease, reverse transcriptase, env, tat, vpu, and rev. Participants are randomized to 1 of 2 groups. People in Group A receive either 2 injections of a lower dose (300 mcg) of the DNA plasmid vaccine or the placebo control. People in Group B receive either 2 injections of a higher dose (3000 mcg) of the DNA plasmid vaccine or the control. Group B will be enrolled only if the vaccine is found to be safe and well-tolerated during the initial 2-week evaluation of all participants in Group A. Participants receive vaccinations administered at Months 0 and 2. All vaccinations are administered by intramuscular (IM) injection in an outpatient setting. Participants have about 10 clinic visits during this study, including the screening and injection visits. Participants give blood and urine samples at study visits. They are tested for HIV before entering the study and 4 more times during the study. Women who can become pregnant may undergo up to 3 pregnancy tests during the study period.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections
Keywords
Injections, Intramuscular, HIV Seronegativity, Plasmids, Vaccines, DNA, HIV Preventive Vaccine

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 1
Masking
Double
Enrollment
30 (false)

8. Arms, Groups, and Interventions

Intervention Type
Biological
Intervention Name(s)
pGA2/JS2 Plasmid DNA Vaccine

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria Participants may be eligible for this study if they: Are between the ages of 18 and 40. Are at low risk of HIV infection. Have access to a participating study site and are available for follow-up for 12 months. Complete a questionnaire to evaluate understanding of the study prior to enrollment. Are willing to receive HIV test results. Are in good general health. Do not have hepatitis B. Are HCV antibody negative or, if HCV antibody positive, are HCV PCR negative. Have had a negative HIV blood test within 8 weeks prior to enrollment. Women of childbearing potential must agree to use acceptable methods of contraception. Note: All inclusion criteria must be assessed within 56 days prior to study entry. Exclusion Criteria Participants may not be eligible for this study if they: Have been immunized against smallpox. Have received HIV vaccines or placebo in a previous HIV vaccine trial. Have used drugs that interfere with the immune system within the past 6 months. Have received blood products within 120 days before HIV screening. Have received immunoglobulin within 60 days before HIV screening. Have received a live vaccine within 30 days prior to initial study vaccine administration. Have used investigational research agents within 30 days prior to initial study vaccine administration. Have received a killed vaccine or allergy treatment injections within 14 days of study vaccine administration. Are currently taking anti-TB therapy. Have a history of serious harmful reactions to vaccines. Have a history of immune system disease. Have a history of unstable asthma. Have a history of type I or type II diabetes. Have a history of thyroid disease. Have a history of tissue swelling with serious episodes. Have a history of high blood pressure. Have a history of a bleeding disorder that was diagnosed by a doctor. Have active syphilis. Have a history of cancer, unless it has been surgically removed and in the opinion of the investigator is not likely to recur during the study period. Have a history of a seizure disorder. Have had their spleen removed. Have mental illness that would interfere with compliance with the protocol. Have any other conditions that, in the judgement of the investigator, would interfere with the study. Are pregnant or breast-feeding. Note: All exclusion criteria must be assessed within 56 days prior to study entry.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mark Mulligan
Organizational Affiliation
University of Alabama at Birmingham
Official's Role
Study Chair
Facility Information:
Facility Name
Alabama Vaccine CRS
City
Birmingham
State/Province
Alabama
Country
United States
Facility Name
UCSF, Gen. Clinical Research Ctr., Mt. Zion Hosp.
City
San Francisco
State/Province
California
ZIP/Postal Code
94102
Country
United States
Facility Name
San Francisco Vaccine and Prevention CRS
City
San Francisco
State/Province
California
Country
United States
Facility Name
FHCRC/UW Vaccine CRS
City
Seattle
State/Province
Washington
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
11050940
Citation
Robinson HL, Pertmer TM. DNA vaccines for viral infections: basic studies and applications. Adv Virus Res. 2000;55:1-74. doi: 10.1016/s0065-3527(00)55001-5. No abstract available.
Results Reference
background
PubMed Identifier
10837079
Citation
Gurunathan S, Klinman DM, Seder RA. DNA vaccines: immunology, application, and optimization*. Annu Rev Immunol. 2000;18:927-74. doi: 10.1146/annurev.immunol.18.1.927.
Results Reference
background
PubMed Identifier
11393868
Citation
Amara RR, Villinger F, Altman JD, Lydy SL, O'Neil SP, Staprans SI, Montefiori DC, Xu Y, Herndon JG, Wyatt LS, Candido MA, Kozyr NL, Earl PL, Smith JM, Ma HL, Grimm BD, Hulsey ML, Miller J, McClure HM, McNicholl JM, Moss B, Robinson HL. Control of a mucosal challenge and prevention of AIDS by a multiprotein DNA/MVA vaccine. Science. 2001 Apr 6;292(5514):69-74. doi: 10.1126/science.1058915.
Results Reference
background
PubMed Identifier
10740236
Citation
Ramshaw IA, Ramsay AJ. The prime-boost strategy: exciting prospects for improved vaccination. Immunol Today. 2000 Apr;21(4):163-5. doi: 10.1016/s0167-5699(00)01612-1. No abstract available.
Results Reference
background

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Safety of an HIV DNA Vaccine Given to HIV Uninfected Adults

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