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Efficacy of Using Interleukin-2 in Antiretroviral Naïve HIV Patients (ANRS119)

Study of the Immunological Efficacy of Using Subcutaneous Interleukin-2 (IL-2) in Antiretroviral Naïve HIV-1-Infected Subjects With a CD4 Cell Count Above 300/mm3. ANRS 119 Trial INTERSTART

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00120185
Enrollment
130
Registered
2005-07-15
Start date
2003-12-01
Completion date
2006-11-01
Last updated
2026-04-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV Infections

Keywords

HIV Infections, Interleukin-2

Brief summary

Interleukin-2 (IL-2) increases the number of CD4 cells in HIV-1 infected patients under highly active antiretroviral therapy (HAART) with a CD4 cell count over 200/mm3, but its activity in patients without antiretroviral therapy is unknown. This study will test the efficacy and safety of IL-2 in naïve patients with a CD4 count between 300 and 500/m3.

Detailed description

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 under antiretroviral therapy and a high level of CD4 cell 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 patient is not receiving antiretroviral therapy is not known. The purpose of this multicentric national study is to compare the effects of IL-2 versus no treatment in HIV naïve patients. One hundred thirty HIV-1-infected patients, with a CD4 count between 300 and 500/mm3, will be randomly assigned to one of two treatment groups : IL-2 or no treatment. 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 5 cycles, ending at Week 96), the first three cycles 8 weeks apart. Evaluation will be done at week 96. The primary endpoint is the proportion of patients reaching an absolute CD4 count below 300/mm3 at Week 96. Secondary endpoints include the occurrence of HIV-related events, drug safety and the evolution of CD4 cells and of HIV RNA and HIV DNA loads over time.

Interventions

DRUGInterleukin-2

Sponsors

French National Agency for Research on AIDS and Viral Hepatitis
Lead SponsorOTHER_GOV
Chiron Corporation
CollaboratorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adult patients with proven HIV-1-infection * No prior exposition to antiretrovirals * CD4 cell count between 300 and 500/mm3 * Signed written inform consent

Exclusion criteria

* Pregnancy

Design outcomes

Primary

MeasureTime frame
Proportion of patients reaching an absolute CD4 count below 300/mm3 at W96

Secondary

MeasureTime frame
Group B or C events (1993 CDC classification of HIV infection)
Initiation of antiretroviral therapy
Evolution of the CD4 count during the study
Time to the first visit with a CD4 count below 300/mm3
Tolerance of IL-2
Evolution of the plasma HIV RNA load
Evolution of the HIV DNA level in PBMCs
Quality of life at W96
Assessment of lipodystrophy at W96
Immunological substudies (CD4 homeostasis, anti HIV cellular immune responses) at W96

Countries

France

Contacts

PRINCIPAL_INVESTIGATORJean-Michel Molina, MD

Hopital Saint Louis Paris service des Maladies infectieuses et Tropicales

STUDY_CHAIRJean-Pierre Aboulker, MD

Inserm SC10

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 4, 2026