HIV Immune and Virological Responses Following the Administration of IL-2 Either Alone or Combined to ALVAC-HIV 1433 and HIV Lipopeptides in Patients Treated Early With HAART During Primary Infection
Primary Purpose
HIV Infection
Status
Terminated
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
IL-2
LIPO-6T
ALVAC VIH 1433
Sponsored by
About this trial
This is an interventional treatment trial for HIV Infection focused on measuring HIV infection, AIDS Vaccines, ALVAC vaccine, Interleukin-2, Antiretroviral Therapy, Highly Active
Eligibility Criteria
Inclusion Criteria: History of symptomatic HIV primary infection with p24 positive or incomplete Western Blot Treatment beginning before 4W after the first primary infection serology HAART with IP or NNRTI since one year, wtih no change since 3 months Viral load below 50 cp since 6 months PN over 1000/mm3;Hb over 10.5g/l;Platelets over 75000/mm3, creatinine below 1.5N; transaminases below 2.5N Exclusion Criteria: Vaccination or chemotherapy or corticosteroid since 3 months Evolutive cancer pregnancy or breastfeeding
Sites / Locations
Outcomes
Primary Outcome Measures
Evolution of CD4-CD8 non specific and HIV specific cells, vaccinal peptids and viral load with DNA proviral at W36
Secondary Outcome Measures
Safety of IL-2, ALVAC and LIPO-6T
Tolerability of HAART
Kinetic of viral load rebound with frequency and delay of cv over 10 000 cp and 50 000 cp
Evolution on immune response and predictive value of immunologic parameters on viral load
Full Information
NCT ID
NCT00196651
First Posted
September 12, 2005
Last Updated
September 12, 2005
Sponsor
French National Agency for Research on AIDS and Viral Hepatitis
Collaborators
Aventis Pharmaceuticals
1. Study Identification
Unique Protocol Identification Number
NCT00196651
Brief Title
HIV Immune and Virological Responses Following the Administration of IL-2 Either Alone or Combined to ALVAC-HIV 1433 and HIV Lipopeptides in Patients Treated Early With HAART During Primary Infection
Official Title
Randomized Study on HIV Immune and Virological Responses Following the Administration of IL-2 Either Alone or Combined to ALVAC-HIV 1433 and HIV Lipopeptides (LIPO-6T) in Patients Treated Early With HAART During Primary Infection. ANRS 095 PRIMOVAC
Study Type
Interventional
2. Study Status
Record Verification Date
September 2005
Overall Recruitment Status
Terminated
Study Start Date
August 2000 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
February 2004 (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
French National Agency for Research on AIDS and Viral Hepatitis
Collaborators
Aventis Pharmaceuticals
4. Oversight
5. Study Description
Brief Summary
HIV-specific immune responses are preserved in patients treated early during primary infection.The trial evaluated whether the addition to HAART of IL-2 alone or combined with an immunization procedure might enhance HIV immune responses and improve viral control after HAART discontinuation
Detailed Description
HIV-specific immune responses are preserved in patients treated early during primary infection. The trial evaluated whether the addition to HAART of IL-2 alone or combined with an immunization procedure might enhance HIV immune responses and improve viral control after HAART discontinuation.Patients treated with HAART are randomized to 3 arms:arm1 HAART alone; arm2 with 5 cycles of IL-2 at wk0 ,8 ,16 ,24 and 32;arm3 4 injections of Alvac-HIV 1433 and LIPO-6T at wk0,4,8 followed by 3 cycles of IL-2 at w 16, 24 and 32. HAART is stopped at wk 40 in patient with undetectable plasma viral load. Viral loads and HIV-specific responses are monitored during the therapeutic period and after HAART interruption until w52. HAARTis rei-initiated with viral failure.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infection
Keywords
HIV infection, AIDS Vaccines, ALVAC vaccine, Interleukin-2, Antiretroviral Therapy, Highly Active
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (false)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
IL-2
Intervention Type
Biological
Intervention Name(s)
LIPO-6T
Intervention Type
Biological
Intervention Name(s)
ALVAC VIH 1433
Primary Outcome Measure Information:
Title
Evolution of CD4-CD8 non specific and HIV specific cells, vaccinal peptids and viral load with DNA proviral at W36
Secondary Outcome Measure Information:
Title
Safety of IL-2, ALVAC and LIPO-6T
Title
Tolerability of HAART
Title
Kinetic of viral load rebound with frequency and delay of cv over 10 000 cp and 50 000 cp
Title
Evolution on immune response and predictive value of immunologic parameters on viral load
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
History of symptomatic HIV primary infection with p24 positive or incomplete Western Blot
Treatment beginning before 4W after the first primary infection serology
HAART with IP or NNRTI since one year, wtih no change since 3 months
Viral load below 50 cp since 6 months
PN over 1000/mm3;Hb over 10.5g/l;Platelets over 75000/mm3, creatinine below 1.5N; transaminases below 2.5N
Exclusion Criteria:
Vaccination or chemotherapy or corticosteroid since 3 months
Evolutive cancer
pregnancy or breastfeeding
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Cecile Goujard, MD
Organizational Affiliation
Hopital Kremlin Bicetre Bicetre France
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jean Pierre Aboulker, MD
Organizational Affiliation
Inserm SC10 France
Official's Role
Study Director
12. IPD Sharing Statement
Citations:
PubMed Identifier
17919105
Citation
Goujard C, Marcellin F, Hendel-Chavez H, Burgard M, Meiffredy V, Venet A, Rouzioux C, Taoufik Y, El Habib R, Beumont-Mauviel M, Aboulker JP, Levy Y, Delfraissy JF; PRIMOVAC-ANRS 095 Study Group. Interruption of antiretroviral therapy initiated during primary HIV-1 infection: impact of a therapeutic vaccination strategy combined with interleukin (IL)-2 compared with IL-2 alone in the ANRS 095 Randomized Study. AIDS Res Hum Retroviruses. 2007 Sep;23(9):1105-13. doi: 10.1089/aid.2007.0047.
Results Reference
derived
Learn more about this trial
HIV Immune and Virological Responses Following the Administration of IL-2 Either Alone or Combined to ALVAC-HIV 1433 and HIV Lipopeptides in Patients Treated Early With HAART During Primary Infection
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