Efficacy of Adding Interleukin-2 to an Optimized Antiretroviral Regimen in HIV Patients in Therapeutic Failure (ANRS123)
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|ClinicalTrials.gov Identifier: NCT00113282|
Recruitment Status : Completed
First Posted : June 8, 2005
Last Update Posted : December 22, 2011
|Condition or disease||Intervention/treatment||Phase|
|HIV Infections||Drug: Interleukin-2 (IL-2)||Phase 2|
IL-2 is produced naturally in the body and helps CD4 cells multiply. In earlier studies in HIV-infection, most of the patients with a controlled viral load and a high level of CD4 count (over 200/mm3) who received IL-2, experienced an increase of their CD4 cell count superior to what is observed with antiretroviral therapy alone.
The efficacy of IL-2 when the viral load is high and the CD4 cell count is low is not known. The purpose of this multicentric national study is to compare the effects of an optimized antiretroviral regimen with or without IL-2.The choice of the antiretroviral regimen will be made from a genotype resistance test.
Ninety eight HIV-1-infected patients experiencing advanced treatment failure with a CD4 count below 200/mm3 and a plasma viral load above 10,000 HIV RNA copies/ml, will be randomly assigned to one of two treatment groups: with or without IL-2.
The group with IL-2 will receive a dose of 4.5 million International units by subcutaneous injection twice a day for 5 days (up to a total of 8 cycles, ending at Week 42), the first two cycles 4 weeks apart, the following cycles 6 weeks apart.
Evaluation will be done at week 52 and further at W76. The primary endpoint is the proportion of patients reaching an absolute CD4 count over 200/mm3 at Week 52. Secondary endpoints include the proportion of patients increasing their CD4 count over 50/mm3 between Week 00 and Week 24,and between Week 00 and Week 52, the occurrence of HIV-related events, drug safety and the evolution of CD4 cells and of HIV RNA and HIV DNA loads over time.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||57 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Official Title:||Study of the Immunological Efficacy of Adding Subcutaneous Interleukin-2 (IL-2) to an Optimized Antiretroviral Regimen in HIV-1-infected Subjects Experiencing Therapeutic Failure on an Ongoing Antiretroviral Combination With a CD4 Cell Count ≤ 200/mm3 ANRS 123 Trial|
|Study Start Date :||June 2004|
|Actual Primary Completion Date :||December 2007|
|Actual Study Completion Date :||February 2008|
- proportion of patients reaching an absolute CD4 count over 200/mm3 at Week 52 (W52)
- group B or C events (1993 CDC classification of HIV infection)between Week 00 and Week 96
- median value of the CD4 count at W52
- evolution of the CD4 count during the study
- time to the first visit with a CD4 count ≥ 200/mm3
- tolerance of IL-2
- tolerance of antiretroviral drugs
- evolution of the plasma HIV RNA load at W64 and W76
- evolution of the HIV DNA level in PBMCs at W64 and W76
- number of modifications of antiretroviral regimen until W52
- clinical status at W64 and W76
- CD4 count at W64, W76 and W96
- plasma HIV RNA load at W64, W76 and W96
- number of modifications of antiretroviral regimen at W64 and W76
- proportion of patients increasing their CD4 count over 50/mm3 between Week 00 and Week 24, and between Week 00 and Week 52
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00113282
|Hôpital Necker service des Maladies Infectieuses|
|Paris, France, 75015|
|Study Chair:||Geneviève Chêne, Pr||Inserm Unite 593|
|Principal Investigator:||Jean Paul VIARD, Dr||Assistance Publique - Hôpitaux de Paris|