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A Study to Evaluate the Effects of Giving Proleukin (rIL-2) to HIV-Positive Patients With CD4 Counts Greater Than 300 Cells/mm3

Phase 3CompletedNCT00000949
National Institute of Allergy and Infectious Diseases (NIAID)460 enrolled

Overview

The purpose of this study is to examine how rIL-2 affects HIV-positive patients with CD4 counts over 300 cells/mm3 who are on anti-HIV drug therapy. The drug rIL-2 has been shown to increase CD4 cell counts, which help the body fight off HIV. There is strong evidence that rIL-2 increases CD4 cell counts (cells of the immune system that fight infection). This study examines the effect of 2 different amounts of rIL-2 on CD4 cell count and the amount of HIV in the blood (viral burden).

There is substantial evidence that rIL-2 increases CD4+ cell count. Whether or not rIL-2 delays progression to AIDS and extends survival is currently unknown, such clinical benefits of rIL-2 can only be established in a large, long-term, randomized trial. This study examines the effect of two different rIL-2 doses on HIV viral burden and CD4+ cell count and provides additional information on optimal dosing, safety, and antiviral activity of rIL-2. Patients are randomized to receive one of two subcutaneous (sc) doses of recombinant rIL-2 or no rIL-2. Those patients who take rIL-2 initially receive three courses of treatment. For this study, a course is defined as eight calendar weeks, including the five-day period of sc rIL-2 administration. Additional courses are given (no more frequently than every 6 weeks) in order to maintain a CD4+ count of at least twice its baseline level or at least 1,000 cells/mm3. Follow-up will continue for all patients until a common closing date of 12 months following enrollment of the last patient.

Study Type

INTERVENTIONAL

Purpose

TREATMENT

Masking

NONE

Enrollment

460

Conditions

HIV Infections

Interventions

AldesleukinDRUG

Eligibility

Sex: ALLMin age: 18 Years
Medical Language ↔ Plain English
Inclusion Criteria You may be eligible for this study if you: * Are HIV-positive. * Agree to practice abstinence or use effective birth control methods during the study. * Are on anti-HIV therapy and have a CD4 count of at least 300 cells/mm3. * Are at least 18 years old. Exclusion Criteria You will not be eligible for this study if you: * Have a history of progressive diseases. * Have a history of severe autoimmune/inflammatory disease. * Have Crohn's disease. * Are taking antiseizure medications or certain other medications. * Are receiving chemotherapy. * Are pregnant or breast-feeding. * Have ever received rIL-2.

Locations (15)

Community Consortium / UCSF

San Francisco, California, United States

Denver CPCRA / Denver Public Hlth

Denver, Colorado, United States

Washington Reg AIDS Prog / Dept of Infect Dis

Washington D.C., District of Columbia, United States

AIDS Research Consortium of Atlanta

Atlanta, Georgia, United States

AIDS Research Alliance - Chicago

Chicago, Illinois, United States

Louisiana Comm AIDS Rsch Prog / Tulane Univ Med

New Orleans, Louisiana, United States

Wayne State Univ - WSU/DMC / Univ Hlth Ctr

Detroit, Michigan, United States

Henry Ford Hosp

Detroit, Michigan, United States

Southern New Jersey AIDS Clinical Trials

Camden, New Jersey, United States

North Jersey Community Research Initiative

Newark, New Jersey, United States

...and 5 more locations

Data from ClinicalTrials.gov

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