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Safety, Tolerability, and Anti-HIV Activity of PEG-Intron in HIV-Positive Children

Phase 1
Completed
Conditions
HIV Infections
Registration Number
NCT00006325
Lead Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
Brief Summary

The purpose of this study is to see if PEG-Intron is safe and tolerated when given to children, to see how much gets into the blood and how long it stays in the blood, and to see how well it works to reduce viral load (level of HIV in the blood).

PEG-Intron is an experimental drug that works differently than other anti-HIV medications. It decreases the ability of HIV to infect the T cells (a special type of cell that helps fight infection). PEG-Intron has been approved by the Food and Drug Administration (FDA) to treat hepatitis C in adults, but in this study, it is being used as an investigational agent for the treatment of HIV/AIDS. It has not been tested in children before and experience with PEG-Intron in adults is limited. (This protocol has been changed to reflect FDA approval of PEG-Intron for treating hepatitic C in adults.)

Detailed Description

The current optimal clinical management of HIV infection involves therapy with combinations of nucleoside and nonnucleoside reverse transcriptase inhibitors and HIV protease inhibitors. These regimens, though effective, do not completely eliminate HIV and the development of drug resistance is a major clinical problem. Interferons have been proposed as a possible treatment of HIV. Interferon-alfa inhibits HIV replication in vitro, and HIV-infected patients appear to have reduced production of interferons. Previous short-term clinical studies in adults showed anti-HIV activity, although there were safety and tolerability problems associated with the higher dose regimens used. This study will utilize a rising multiple-dose design to assess the safety, tolerability, and pharmacokinetics of single and multiple doses of PEG-Intron in HIV-infected children.

In a dose-escalation study, patients add weekly PEG-Intron to their antiretroviral therapy for up to 6 weeks. The first 2 doses are received in the clinic where parents/guardians are trained to administer injections, and succeeding doses are given at home.

Patients are enrolled from 2 cohorts. An older cohort of ages 2 to 16 years receives PEG-Intron at the lowest drug level. If the dose is tolerated, patients are added and if safety criteria are met, patients are enrolled in the next higher dose level. The dose level will be increased similarly for up to 4 doses. An optimal dose level is chosen.

Cohort II patients are a younger group ranging from 3 months to under 2 years of age. Patients initially receive the next lower PEG-Intron dose to the optimal dose identified in Cohort I \[AS PER AMENDMENT 07/23/01: or 1 microg/kg if the optimal dose proves to be 1 microg/kg\]. If this dose is safely tolerated, additional patients are added. If this dose level meets safety criteria, patients are enrolled to receive the optimal dose level. Patients are evaluated with the same safety criteria as Cohort I. Patients in both cohorts who have at least a 0.5 log reduction in HIV RNA at 28 days of treatment are offered continued treatment for a total of 60 weeks.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
54
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (15)

Children's Hosp of Los Angeles/UCLA Med Ctr

🇺🇸

Los Angeles, California, United States

Los Angeles County - USC Med Ctr

🇺🇸

Los Angeles, California, United States

SUNY Health Sciences Ctr at Syracuse / Pediatrics

🇺🇸

Syracuse, New York, United States

Children's Hosp of Boston

🇺🇸

Boston, Massachusetts, United States

Texas Children's Hosp / Baylor Univ

🇺🇸

Houston, Texas, United States

UCSF / Moffitt Hosp - Pediatric

🇺🇸

San Francisco, California, United States

Univ of Miami (Pediatric)

🇺🇸

Miami, Florida, United States

Univ of Florida Health Science Ctr / Pediatrics

🇺🇸

Jacksonville, Florida, United States

Connecticut Children's Med Ctr

🇺🇸

Farmington, Connecticut, United States

Univ of Medicine & Dentistry of New Jersey / Univ Hosp

🇺🇸

Newark, New Jersey, United States

Schneider Children's Hosp

🇺🇸

New Hyde Park, New York, United States

Univ of Massachusetts Med School

🇺🇸

Worcester, Massachusetts, United States

Long Beach Memorial (Pediatric)

🇺🇸

Long Beach, California, United States

Baystate Med Ctr of Springfield

🇺🇸

Springfield, Massachusetts, United States

Harlem Hosp Ctr

🇺🇸

New York, New York, United States

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