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COMPLETED Phase 2

Interferon Alfa in Treating Children With HIV-Related Cancer

NCT00002621 · View on ClinicalTrials.gov ↗

Study Summary

RATIONALE: Interferon alfa may interfere with the growth of cancer cells. PURPOSE: Phase II trial to study the effectiveness of interferon alfa in treating children with an HIV-related cancer including leukemia, non-Hodgkin's lymphoma, CNS lymphoma, or other solid tumors.

Interventions

  • BIOLOGICAL recombinant interferon alfa

Study Locations (10)

Texas

  • Medical City Dallas Hospital — Dallas
  • San Antonio Military Pediatric Cancer and Blood Disorders Center — Lackland Air Force Base
  • University of Texas Health Science Center at San Antonio — San Antonio

Other

  • University of Puerto Rico School of Medicine Medical Sciences Campus — San Juan
  • Clinique de Pediatrie — Geneva

Kansas

  • Via Christi Regional Medical Center — Wichita

Louisiana

  • MBCCOP - LSU Health Sciences Center — New Orleans

New Jersey

  • Tomorrows Children's Institute — Hackensack

North Carolina

  • Mission Saint Joseph's Health System — Asheville

Quebec

  • McGill University Health Center - Montreal Children's Hospital — Montreal

Trial Details

FieldValue
Enrollment Target 8 participants
Start Date 1994-12
Est. Completion 2005-09
Phase Phase 2

Sponsor

Children's Oncology Group

318 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00002621

The ClinicalTrials.gov registry entry for NCT00002621 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 8 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Children's Oncology Group, which has 318 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Lymphoma appearing as the primary indexed condition, and to 1 intervention — of which recombinant interferon alfa is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00002621 reports 10 study locations spanning 7 distinct geographic areas — top geographies include Texas, Other, Kansas. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00002621 about?

NCT00002621 is a clinical study titled "Interferon Alfa in Treating Children With HIV-Related Cancer". RATIONALE: Interferon alfa may interfere with the growth of cancer cells. PURPOSE: Phase II trial to study the effectiveness of interferon alfa in treating children with an HIV-related cancer including leukemia, non-Hodgkin's lymphoma, CNS lymphoma, or other solid tumors.

What is the current status of trial NCT00002621?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 8 participants. The study started on 1994-12. Estimated completion is 2005-09.

What conditions does trial NCT00002621 study?

This clinical trial studies the following conditions: Lymphoma, Leukemia, Unspecified Childhood Solid Tumor, Protocol Specific. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00002621?

The interventions under investigation include: recombinant interferon alfa (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00002621?

This trial is sponsored by Children's Oncology Group, which has 318 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00002621 being conducted?

This trial has 10 study locations across Kansas, Louisiana, New Jersey, North Carolina, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial