AIDS Vaccine Study Comparing Immunogenicity and Safety of 3 Doses of Lipopeptides Versus Placebo in Non Infected HIV Volunteers
NCT ID: NCT00121758
Last Updated: 2008-06-06
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE2
156 participants
INTERVENTIONAL
2004-09-30
2007-12-31
Brief Summary
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Detailed Description
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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.
Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
DOUBLE
Interventions
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LIPO-5
Eligibility Criteria
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Inclusion Criteria
* 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
* 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
21 Years
55 Years
ALL
Yes
Sponsors
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French National Agency for Research on AIDS and Viral Hepatitis
OTHER_GOV
Aventis Pharmaceuticals
INDUSTRY
Principal Investigators
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Dominique Salmon, MD
Role: PRINCIPAL_INVESTIGATOR
Hopital Cochin Paris. Centre des essais vaccinaux Cochin Pasteur
Christine Durier
Role: STUDY_CHAIR
Inserm SC10
Locations
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CIC de Vaccinologie Cochin Pasteur
Paris, , France
Countries
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References
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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.
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.
Other Identifiers
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ANRS VAC18
Identifier Type: -
Identifier Source: secondary_id
2004-000233-10
Identifier Type: -
Identifier Source: org_study_id