Phase I Safety and Immunogenicity Trial of Vaccinia-HIV Envelope Recombinant Vaccine (HIVAC-1e) in Combination With Soluble Recombinant Envelope Vaccine (gp160; VaxSyn)
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Purpose
To determine if priming (giving the first vaccination) with a vaccinia recombinant (HIVAC-1e) provides a significant advantage in immunogenicity (production of antibodies) compared to priming with a soluble recombinant protein (gp160); to learn more about the safety of the combination use of the two HIV envelope vaccines utilized in the study.
Recent studies at the AIDS vaccine units have shown the safety of two candidate HIV vaccines, HIVAC-1e and gp160. Specific questions to be addressed in this part of the study include: Does combination vaccination result in a synergistic (added) response not predicted by just the addition of a second vaccination, and does this synergism depend on the unique priming effect of a vaccinia recombinant, or will any combination do?
| Condition | Intervention | Phase |
|---|---|---|
|
HIV Infections |
Biological: HIVAC-1e Biological: gp160 Vaccine (MicroGeneSys) |
Phase 1 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Primary Purpose: Prevention |
| Official Title: | Phase I Safety and Immunogenicity Trial of Vaccinia-HIV Envelope Recombinant Vaccine (HIVAC-1e) in Combination With Soluble Recombinant Envelope Vaccine (gp160; VaxSyn) |
| Estimated Enrollment: | 35 |
| Study Completion Date: | December 1992 |
Recent studies at the AIDS vaccine units have shown the safety of two candidate HIV vaccines, HIVAC-1e and gp160. Specific questions to be addressed in this part of the study include: Does combination vaccination result in a synergistic (added) response not predicted by just the addition of a second vaccination, and does this synergism depend on the unique priming effect of a vaccinia recombinant, or will any combination do?
Volunteers will be randomized to one of four groups. Group A (20 volunteers) will receive gp160 (VaxSyn) followed two months later by a repeat dose. Group B (20 volunteers) will receive VaxSyn followed two months later by HIVAC-1e. Group C (20 volunteers) will receive HIVAC-1e followed two months later by VaxSyn. Group D (10 volunteers) will receive HIVAC-1e followed two months later by HIVAC-1e. For volunteers in Groups A, B, and C who do not react to the initial vaccination, a second attempt to obtain a reaction may be made 7 or more days following the initial inoculation. Per addendum, two additional booster inoculations are given: one at 6 months or later post initial inoculation (Groups A, C, and D receive VaxSyn and Group B receives HIVAC-1e) and another at 12 months or later (all Groups receive VaxSyn).
Eligibility| Ages Eligible for Study: | 18 Years to 60 Years (Adult) |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria
- Volunteers must be healthy adults without high-risk behavior for HIV-1 infection and with history of smallpox vaccination more than 5 years prior to enrollment.
Exclusion Criteria
Co-existing Condition:
Patients with the following symptoms and conditions are excluded:
- Identifiable high-risk behavior for HIV infection including active intravenous drug use and multiple sexual partners or sexual contact with high-risk partners within the past 6 months.
- Eczema, active or within the past year.
- Household contact with someone who is pregnant.
- Household contact with children less than 12 years old.
- Household contact with anyone with eczema.
- Household contact with anyone with immunodeficiencies.
- Hypersensitivity to insects.
- Medical or psychiatric conditions that would make compliance unlikely.
- Evidence of depression.
Patients with the following prior conditions are excluded:
- History of immunodeficiency or chronic illness or use of immunosuppressive medications.
- Blood or blood product transfusion within previous six months.
- Eczema, active or within the past year.
- Prior receipt of experimental HIV vaccine. [Specific other requirements are stated elsewhere in the record.]
Prior Treatment:
Excluded within 6 months prior to study entry:
- Blood or blood product transfusions.
Risk Behavior:
Excluded:
- Active intravenous drug use.
- Syphilis, gonorrhea, or any sexually transmitted diseases including chlamydia or pelvic inflammatory disease within the past 6 months.
- More than 2 sexual partners in the past 6 months or sexual contact with a high-risk partner.
Contacts and LocationsPlease refer to this study by its ClinicalTrials.gov identifier: NCT00000630
| United States, Tennessee | |
| Vanderbilt Univ. Hosp. AVEG | |
| Nashville, Tennessee, United States, 37232 | |
| United States, Washington | |
| UW - Seattle AVEG | |
| Seattle, Washington, United States, 981050371 | |
| Study Chair: | Koff W |
More Information
| Responsible Party: | National Institute of Allergy and Infectious Diseases (NIAID) |
| ClinicalTrials.gov Identifier: | NCT00000630 History of Changes |
| Other Study ID Numbers: | AVEG 002A 10538 |
| Study First Received: | November 2, 1999 |
| Last Updated: | May 22, 2012 |
| Health Authority: | United States: Federal Government |
Keywords provided by National Institute of Allergy and Infectious Diseases (NIAID):
|
Vaccines, Synthetic Vaccinia Virus Viral Envelope Proteins Acquired Immunodeficiency Syndrome |
AIDS Vaccines HIV Seronegativity HIV Preventive Vaccine |
Additional relevant MeSH terms:
|
HIV Infections Vaccinia Lentivirus Infections Retroviridae Infections RNA Virus Infections Virus Diseases Sexually Transmitted Diseases, Viral Sexually Transmitted Diseases |
Immunologic Deficiency Syndromes Immune System Diseases Poxviridae Infections DNA Virus Infections Vaccines Immunologic Factors Physiological Effects of Drugs |
ClinicalTrials.gov processed this record on September 26, 2016