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Completed Phase 1 Interventional

A Study to Test the Safety of Recombinant Interleukin-2 (rIL-2) in HIV-Infected Children

ClinicalTrials.gov ID: NCT00000849

Public ClinicalTrials.gov record NCT00000849. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 5, 2026, 4:42 AM EST

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Official title

Phase I/II Trial of Recombinant Interleukin-2 In Symptomatic Human Immunodeficiency Virus-Infected Children

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to determine the safety and maximum tolerated dose (the highest dose that can be given safely) of recombinant Interleukin-2 (rIL-2) in HIV-infected children. This study also evaluates the effect of rIL-2 on the immune system of these patients. IL-2 is a substance naturally produced by the body's white blood cells that plays an important role in helping the body fight infection. HIV-infected patients do not produce enough IL-2, and it is hoped that the use of rIL-2 may improve immune system function in these patients. First, it is necessary to determine the safety and effectiveness of this drug in HIV-infected children.

Study identification

NCT ID
NCT00000849
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Enrollment
27 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
3 Years to 12 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Not listed
Primary completion
Not listed
Completion
Mar 2001 (Actual)
Last update posted
Oct 29, 2021

Ends 2001

United States locations

U.S. sites
14
U.S. states
10
U.S. cities
11
Facility City State ZIP Site status
Long Beach Memorial Med. Ctr., Miller Children's Hosp. Long Beach California 90801 —
UCSF Pediatric AIDS CRS San Francisco California 941430105 —
Univ. of Colorado Denver NICHD CRS Aurora Colorado 802181088 —
Univ. of Florida Jacksonville NICHD CRS Jacksonville Florida 32209 —
Chicago Children's CRS Chicago Illinois 606143394 —
Univ. of Chicago - Dept. of Peds., Div. of Infectious Disease Chicago Illinois 606371470 —
Tulane/LSU Maternal/Child CRS New Orleans Louisiana 701122699 —
HMS - Children's Hosp. Boston, Div. of Infectious Diseases Boston Massachusetts 021155724 —
NYU Med. Ctr., Dept. of Medicine New York New York 10016 —
Columbia IMPAACT CRS New York New York 10032 —
Incarnation Children's Ctr. New York New York 10032 —
The Children's Hosp. of Philadelphia IMPAACT CRS Philadelphia Pennsylvania 191044318 —
Texas Children's Hosp. CRS Houston Texas 77030 —
VCU Health Systems, Dept. of Peds Richmond Virginia 23219 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00000849, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 29, 2021 · Synced Nov 5, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00000849 live on ClinicalTrials.gov.

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