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Cytokine

Proleukin plus antiretroviral therapy for HIV/AIDS (SILCAAT Trial)

Phase 3
Waitlist Available
Led By James D Neaton, PhD
Research Sponsored by University of Minnesota
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up from randomization to date last known to be alive or november 15, 2008, whichever is earlier
Awards & highlights

Summary

This study will examine whether interleukin-2 (IL-2) plus antiretroviral therapy (ART) slows HIV disease progression in patients with low CD4+ T cell counts compared with patients taking ART alone. CD4+ T cells are a subset of lymphocytes-white blood cells that are part of the body's immune system. IL-2 is a protein that is naturally produced by lymphocytes. Given in intermittent cycles, IL-2 can raise CD4+ T cell counts in some HIV-infected patients taking antiretroviral drugs. This study will examine whether the increase in CD4+ T cells lowers the risk of AIDS-related illnesses and death. HIV-infected patients 18 years of age and older with a viral load under 10,000 copies per milliliter and a CD4+ T cell count between 50 and 299 cells per cubic millimeter who are taking antiretroviral therapy and who have not previously received IL-2 therapy may be eligible for this study. Candidates will be screened with a medical history, physical examination, and blood and urine tests. Participation in the study will be from 4.5 to 6 years, depending on what point in the duration of the study the individual patient is enrolled. Patients will be randomly assigned to receive IL-2 plus ART or ART alone. All participants will be advised individually about the best ART regimen for them. Patients in the IL-2 treatment group will be taught how to self-inject IL-2 under the skin (similar to insulin injections). They will inject IL-2 twice a day for 5 days every 8 weeks for the first year (until week 49 of the study). From week 49 on they may receive 5-day cycles of IL-2 every 4 months when needed to maintain CD4+ T cell count elevations. An extra cycle may be given 2 months after the week 49 follow-up visit (see follow-up schedule below), depending on their CD4+ T cell count. Patients whose cell counts have not increased after 12 to 16 months of IL-2 treatment will discuss with the doctor the possibility of stopping IL-2. Those who do stop IL-2 treatment will be asked to remain in the study for follow-up evaluations. All patients will be followed in the clinic every 2 months for the first year of the study (weeks 1, 9, 17, 25, 33, 41 and 49) and every 4 months during years 2-6 for a brief history and physical exam, urine and blood tests, return of diary cards (record of drug side effects) and medication review. During the visits from the second year on, patients will also be asked about their ability to do certain ordinary tasks, such as taking care of themselves; ...

Eligible Conditions
  • HIV/AIDS

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~from randomization to date last known to be alive or november 15, 2008, whichever is earlier
This trial's timeline: 3 weeks for screening, Varies for treatment, and from randomization to date last known to be alive or november 15, 2008, whichever is earlier for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
New or Recurrent Disease Progression Events, as Defined, or Death.
Secondary study objectives
All-cause Mortality
CD4+ Cell Count
Grade 4 Clinical Events
+2 more

Side effects data

From 2007 Phase 3 trial • 1695 Patients • NCT00013611
3%
Infections - pathogen unspecified
2%
Cornoary artery disorders
2%
Bacterial infectious disorders
1%
Gastrointestinal neoplasms malignant and unspecified
1%
Exocrine pancreas conditions
1%
Gastrointestinal haemorrhages NEC
1%
Gastrointestinal motility and defaecation conditions
1%
Hepatic and hepatobiliary disorders
1%
Central nervous system vascular disorders
1%
Joint disorders
1%
Respiratory disorders NEC
1%
Heart failures
1%
Renal disorders (excl nephropathies)
1%
Aneamias nonhaemolytic and marrow depression
1%
Gallbladder disorders
1%
Viral infectious disorders
1%
Injuries NEC
1%
Procedural and device related injuries and complications NEC
1%
Respiratory and mediastinal neoplams malignant and unspecified
100%
80%
60%
40%
20%
0%
Study treatment Arm
Antiretroviral Therapy Only
Proleukin Plus Antiretroviral Therapy

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Proleukin plus antiretroviral therapyExperimental Treatment1 Intervention
Group II: Antiretroviral therapy aloneActive Control1 Intervention
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Aldesleukin
FDA approved

Find a Location

Who is running the clinical trial?

University of MinnesotaLead Sponsor
1,414 Previous Clinical Trials
1,559,663 Total Patients Enrolled
National Institute of Allergy and Infectious Diseases (NIAID)NIH
3,308 Previous Clinical Trials
5,624,365 Total Patients Enrolled
James D Neaton, PhDPrincipal InvestigatorUniversity of Minnesota
1 Previous Clinical Trials
4,688 Total Patients Enrolled
~69 spots leftby Sep 2025