search
Back to results

AIDS Vaccine Study Comparing Immunogenicity and Safety of 3 Doses of Lipopeptides Versus Placebo in Non Infected HIV Volunteers

Primary Purpose

HIV Infections

Status
Completed
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
LIPO-5
Sponsored by
French National Agency for Research on AIDS and Viral Hepatitis
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional prevention trial for HIV Infections focused on measuring HIV Vaccines, HIV Seronegativity

Eligibility Criteria

21 Years - 55 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Healthy volunteers selected by ANRS (French National Agency for Research on AIDS and Viral Hepatitis) For woman of child-bearing age: use of effective contraception Ability to sign informed consent Beneficiary subjects of social security regimen-- Hepatitis B, hepatitis C, HIV, HTLV1 infection and syphilis negative Hemoglobin over 12.5 g/dl for women and over 13.5 g/dl for men Exclusion Criteria: Previous participation in an HIV clinical trial Volunteers with risk to contract HIV infection during the trial Previous vaccination in the last month, and volunteers requiring vaccination during the trial Gift of blood in the last 2 months Eczema, urticaria Medical history of food allergy, Lyell or Stevens Johnson syndrome and aggravated asthma Previous (last 6 months) or ongoing administration of immunological treatment, chemotherapy, radiotherapy or corticosteroid Medical history of autoimmune disease Clinical or biological aftermath of previous disease Medical history of uveitis Transfusion in the last 6 months

Sites / Locations

  • CIC de Vaccinologie Cochin Pasteur

Outcomes

Primary Outcome Measures

Percentage of patients with CD8 immune response on ELISPOT IFN-gamma at week (W) 48

Secondary Outcome Measures

Local and general adverse events
Percentage of subjects with CD4 immune response against different peptides of LIPO-5
Percentage of subjects with sustained response at week 48
Percentage of subjects with response against more than 1 peptide (multiepitopic response)

Full Information

First Posted
July 18, 2005
Last Updated
June 5, 2008
Sponsor
French National Agency for Research on AIDS and Viral Hepatitis
Collaborators
Aventis Pharmaceuticals
search

1. Study Identification

Unique Protocol Identification Number
NCT00121758
Brief Title
AIDS Vaccine Study Comparing Immunogenicity and Safety of 3 Doses of Lipopeptides Versus Placebo in Non Infected HIV Volunteers
Official Title
Randomised Double Blinded Phase II AIDS Vaccine Study Comparing Immunogenicity and Safety of 3 Doses of Lipopeptide (LIPO-5) Versus Placebo in Non Infected HIV Volunteers (ANRS VAC 18)
Study Type
Interventional

2. Study Status

Record Verification Date
June 2008
Overall Recruitment Status
Completed
Study Start Date
September 2004 (undefined)
Primary Completion Date
November 2007 (Actual)
Study Completion Date
December 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
French National Agency for Research on AIDS and Viral Hepatitis
Collaborators
Aventis Pharmaceuticals

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study will test the safety and immune response to an experimental HIV vaccine, LIPO-5, in healthy volunteers. LIPO-5 contains 5 lipopeptides from gag, nef and pol corresponding to more than 50 epitopes. LIPO-5 has been shown to be immunogenic and well tolerated in a first phase I trial in non-HIV infected volunteers. Lower doses of each peptide could have a similar immunogenicity.
Detailed Description
The aims of HIV lipopeptide vaccination approach are to improve cell mediated immune responses in order to obtain strong, long lasting and polyepitopic responses and to focus these responses on highly conserved and immunogenic epitopes. Lipopeptides are chemically synthetized peptides, bearing HIV epitopes, covalently bound to a fatty acid moiety, a monopalmtoyl chain in this case. This lipid chain produces internalization of the lipopeptide into the cytoplasm of the antigen presenting cells. Combinations of several lipopeptides containing sequences from different HIV proteins are used in vaccination trials in order to increase polyepitopic responses. Lipopeptides have been synthetized by the French National Agency for Research on AIDS and Viral Hepatitis (ANRS) preventive program by the group of Helen Gras following a long and meticulous work of epitope screening performed by the team of Jean-Gérard Guillet at the Cochin Institute in Paris. The epitopes were selected on the basis of their strong affinity for HLA class I molecule, on their ability to form a stable complex with these molecules, and on the capacity of these epitopes to be recognized by T cells. The selected peptides are those containing the richest array of epitopes and those most frequently recognized by HIV infected patients. Each peptide has a length of 23 to 32 amino acids (AA). Different types of lipopeptides constructs have been tested in humans. Among these constructs, LIPO-5 contains 5 lipopeptides from gag, nef and pol corresponding to more than 50 epitopes. LIPO-5 has been shown to be immunogenic and well tolerated in a first phase I trial in non-HIV infected volunteers. Lower doses of each peptide could have a similar immunogenicity.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections
Keywords
HIV Vaccines, HIV Seronegativity

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
156 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Biological
Intervention Name(s)
LIPO-5
Primary Outcome Measure Information:
Title
Percentage of patients with CD8 immune response on ELISPOT IFN-gamma at week (W) 48
Secondary Outcome Measure Information:
Title
Local and general adverse events
Title
Percentage of subjects with CD4 immune response against different peptides of LIPO-5
Title
Percentage of subjects with sustained response at week 48
Title
Percentage of subjects with response against more than 1 peptide (multiepitopic response)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Healthy volunteers selected by ANRS (French National Agency for Research on AIDS and Viral Hepatitis) For woman of child-bearing age: use of effective contraception Ability to sign informed consent Beneficiary subjects of social security regimen-- Hepatitis B, hepatitis C, HIV, HTLV1 infection and syphilis negative Hemoglobin over 12.5 g/dl for women and over 13.5 g/dl for men Exclusion Criteria: Previous participation in an HIV clinical trial Volunteers with risk to contract HIV infection during the trial Previous vaccination in the last month, and volunteers requiring vaccination during the trial Gift of blood in the last 2 months Eczema, urticaria Medical history of food allergy, Lyell or Stevens Johnson syndrome and aggravated asthma Previous (last 6 months) or ongoing administration of immunological treatment, chemotherapy, radiotherapy or corticosteroid Medical history of autoimmune disease Clinical or biological aftermath of previous disease Medical history of uveitis Transfusion in the last 6 months
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dominique Salmon, MD
Organizational Affiliation
Hopital Cochin Paris. Centre des essais vaccinaux Cochin Pasteur
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Christine Durier
Organizational Affiliation
Inserm SC10
Official's Role
Study Chair
Facility Information:
Facility Name
CIC de Vaccinologie Cochin Pasteur
City
Paris
ZIP/Postal Code
75014
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
23759749
Citation
Richert L, Hue S, Hocini H, Raimbault M, Lacabaratz C, Surenaud M, Wiedemann A, Tisserand P, Durier C, Salmon D, Lelievre JD, Chene G, Thiebaut R, Levy Y; ANRS Vaccine Network/Vaccine Research Institute. Cytokine and gene transcription profiles of immune responses elicited by HIV lipopeptide vaccine in HIV-negative volunteers. AIDS. 2013 Jun 1;27(9):1421-31. doi: 10.1097/QAD.0b013e32835f5b60.
Results Reference
derived
PubMed Identifier
20625264
Citation
Salmon-Ceron D, Durier C, Desaint C, Cuzin L, Surenaud M, Hamouda NB, Lelievre JD, Bonnet B, Pialoux G, Poizot-Martin I, Aboulker JP, Levy Y, Launay O; ANRS VAC18 trial group. Immunogenicity and safety of an HIV-1 lipopeptide vaccine in healthy adults: a phase 2 placebo-controlled ANRS trial. AIDS. 2010 Sep 10;24(14):2211-23. doi: 10.1097/QAD.0b013e32833ce566.
Results Reference
derived

Learn more about this trial

AIDS Vaccine Study Comparing Immunogenicity and Safety of 3 Doses of Lipopeptides Versus Placebo in Non Infected HIV Volunteers

We'll reach out to this number within 24 hrs