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A Phase I Safety and Immunogenicity Study of HIV p17/p24:Ty-VLP in HIV-1 Seronegative Subjects

Primary Purpose

HIV Infections

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
HIV p17/p24:Ty-VLP
Aluminum hydroxide
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 Vaccines, Synthetic, Recombinant Proteins, HIV-1, AIDS Vaccines, HIV Core Protein p24, p24-VLP vaccine, Gene Products, gag, HIV Seronegativity, HIV Preventive Vaccine

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria Concurrent Medication: Required: Omeprazole given concurrently in patients receiving the oral vaccine dose. Volunteers must have: HIV-1 negativity. Normal history and physical exam. Lower risk for HIV infection. CD4 count >= 400 cells/mm3. Normal urine dipstick with esterase and nitrite. NOTE: No more than 10 percent of volunteers may be over age 50. Exclusion Criteria Co-existing Condition: Volunteers with the following conditions are excluded: Positive for hepatitis B surface antigen. Medical or psychiatric condition (including recent suicidal ideation or present psychosis) that precludes compliance. Occupational responsibilities that preclude compliance. Active syphilis (NOTE: If serology is documented to be a false positive or due to a remote (> 6 months) infection, subject is eligible). Active tuberculosis (NOTE: Subjects with a positive PPD and normal x-ray showing no evidence of TB and who do not require INH therapy are eligible). Volunteers with the following prior conditions are excluded: History of immunodeficiency, chronic illness, malignancy, autoimmune disease, or use of immunosuppressive medications. History of cancer unless surgically excised with reasonable assurance of cure. History of suicide attempts or past psychosis. History of anaphylaxis or other serious adverse reactions to vaccines. History of serious allergic reaction requiring hospitalization or emergent medical care. Prior Medication: Excluded: Prior HIV-1 vaccines or placebo in an HIV vaccine trial. Live attenuated vaccines within the past 60 days. NOTE: Medically indicated subunit or killed vaccines (e.g., influenza, pneumococcal) do not exclude but should be administered at least 2 weeks prior to HIV immunizations. Experimental agents within the past 30 days. Prior Treatment: Excluded: Blood products or immunoglobulin within the past 6 months. Higher risk behavior for HIV infection as determined by screening questionnaire, including: History of injection drug use within the past year. Higher or intermediate risk sexual behavior.

Sites / Locations

  • Univ. of Rochester AVEG

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
November 2, 1999
Last Updated
October 28, 2021
Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
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1. Study Identification

Unique Protocol Identification Number
NCT00001053
Brief Title
A Phase I Safety and Immunogenicity Study of HIV p17/p24:Ty-VLP in HIV-1 Seronegative Subjects
Official Title
A Phase I Safety and Immunogenicity Study of HIV p17/p24:Ty-VLP in HIV-1 Seronegative Subjects
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Completed
Study Start Date
undefined (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
March 1996 (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
To evaluate the safety and immunogenicity of HIV p17/p24:Ty-VLP (virus-like particles) vaccine in uninfected volunteers. Specifically, to determine whether the vaccine formulated with and without alum induces CD8+ cytotoxic T lymphocytes ( CTLs ) that may be cross-reactive against multiple HIV-1 stains. Also, to determine whether boosting with the vaccine orally or rectally will help induce mucosal antibody responses. Induction of CD8+ CTL activity is considered a critical property for a candidate vaccine. Additionally, since the majority of HIV-1 infections occur after inoculation of a mucosal surface, it is desirable to induce mucosal immunity as well as systemic immunity. The HIV p17/p24:Ty-VLP vaccine may potentially induce both CTL and mucosal antibody responses against HIV-1.
Detailed Description
Induction of CD8+ CTL activity is considered a critical property for a candidate vaccine. Additionally, since the majority of HIV-1 infections occur after inoculation of a mucosal surface, it is desirable to induce mucosal immunity as well as systemic immunity. The HIV p17/p24:Ty-VLP vaccine may potentially induce both CTL and mucosal antibody responses against HIV-1. Volunteers receive HIV p17/p24:Ty-VLP vaccine or placebo by IM injection (with or without alum adjuvant) at months 0, 2, and 6, and then either by mouth or rectal enema at months 10 and 11. Volunteers who receive oral vaccine boosting will receive concurrent omeprazole to decrease stomach acid.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections
Keywords
Vaccines, Synthetic, Recombinant Proteins, HIV-1, AIDS Vaccines, HIV Core Protein p24, p24-VLP vaccine, Gene Products, gag, HIV Seronegativity, HIV Preventive Vaccine

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 1
Masking
Double
Enrollment
36 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Biological
Intervention Name(s)
HIV p17/p24:Ty-VLP
Intervention Type
Biological
Intervention Name(s)
Aluminum hydroxide

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria Concurrent Medication: Required: Omeprazole given concurrently in patients receiving the oral vaccine dose. Volunteers must have: HIV-1 negativity. Normal history and physical exam. Lower risk for HIV infection. CD4 count >= 400 cells/mm3. Normal urine dipstick with esterase and nitrite. NOTE: No more than 10 percent of volunteers may be over age 50. Exclusion Criteria Co-existing Condition: Volunteers with the following conditions are excluded: Positive for hepatitis B surface antigen. Medical or psychiatric condition (including recent suicidal ideation or present psychosis) that precludes compliance. Occupational responsibilities that preclude compliance. Active syphilis (NOTE: If serology is documented to be a false positive or due to a remote (> 6 months) infection, subject is eligible). Active tuberculosis (NOTE: Subjects with a positive PPD and normal x-ray showing no evidence of TB and who do not require INH therapy are eligible). Volunteers with the following prior conditions are excluded: History of immunodeficiency, chronic illness, malignancy, autoimmune disease, or use of immunosuppressive medications. History of cancer unless surgically excised with reasonable assurance of cure. History of suicide attempts or past psychosis. History of anaphylaxis or other serious adverse reactions to vaccines. History of serious allergic reaction requiring hospitalization or emergent medical care. Prior Medication: Excluded: Prior HIV-1 vaccines or placebo in an HIV vaccine trial. Live attenuated vaccines within the past 60 days. NOTE: Medically indicated subunit or killed vaccines (e.g., influenza, pneumococcal) do not exclude but should be administered at least 2 weeks prior to HIV immunizations. Experimental agents within the past 30 days. Prior Treatment: Excluded: Blood products or immunoglobulin within the past 6 months. Higher risk behavior for HIV infection as determined by screening questionnaire, including: History of injection drug use within the past year. Higher or intermediate risk sexual behavior.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Spearman P
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Graham B
Official's Role
Study Chair
Facility Information:
Facility Name
Univ. of Rochester AVEG
City
Rochester
State/Province
New York
ZIP/Postal Code
14642
Country
United States

12. IPD Sharing Statement

Citations:
Citation
Martin SJ, Weber J, Roitt I, Matear P, Jones K, Vyakarnam A. Recombinant HIV-1 gag p24-Ty virus-like particles (VLP's) induce HIV-1 p24-specific T helper cells in seronegative volunteers vaccinated with these particles. Int Conf AIDS. 1992 Jul 19-24;8(2):A35 (abstract no PoA 2194)
Results Reference
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PubMed Identifier
7483805
Citation
Weber J, Cheinsong-Popov R, Callow D, Adams S, Patou G, Hodgkin K, Martin S, Gotch F, Kingsman A. Immunogenicity of the yeast recombinant p17/p24:Ty virus-like particles (p24-VLP) in healthy volunteers. Vaccine. 1995 Jun;13(9):831-4. doi: 10.1016/0264-410x(94)00061-q.
Results Reference
background
PubMed Identifier
8267904
Citation
Martin SJ, Vyakarnam A, Cheingsong-Popov R, Callow D, Jones KL, Senior JM, Adams SE, Kingsman AJ, Matear P, Gotch FM, et al. Immunization of human HIV-seronegative volunteers with recombinant p17/p24:Ty virus-like particles elicits HIV-1 p24-specific cellular and humoral immune responses. AIDS. 1993 Oct;7(10):1315-23.
Results Reference
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Learn more about this trial

A Phase I Safety and Immunogenicity Study of HIV p17/p24:Ty-VLP in HIV-1 Seronegative Subjects

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