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COMPLETED Phase 1

Busulfan in Treating Children and Adolescents With Refractory CNS Cancer

NCT00006246 · View on ClinicalTrials.gov ↗

Study Summary

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. PURPOSE: Phase I trial to study the safety of delivering intrathecal busulfan in children and adolescents who have refractory CNS cancer and to estimate the maximum tolerated dose of this treatment regimen.

Interventions

  • DRUG busulfan

Study Locations (8)

Pennsylvania

  • Children's Hospital of Philadelphia — Philadelphia
  • Children's Hospital of Pittsburgh — Pittsburgh

California

  • UCSF Cancer Center and Cancer Research Institute — San Francisco

District of Columbia

  • Children's National Medical Center — Washington D.C.

Massachusetts

  • Dana-Farber Cancer Institute — Boston

North Carolina

  • Duke Comprehensive Cancer Center — Durham

Texas

  • Baylor College of Medicine — Houston

Washington

  • Children's Hospital and Regional Medical Center - Seattle — Seattle

Trial Details

FieldValue
Enrollment Target 28 participants
Start Date 2000-11
Phase Phase 1

Sponsor

Pediatric Brain Tumor Consortium

8 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00006246

The ClinicalTrials.gov registry entry for NCT00006246 describes a study currently listed as completed. It is categorized as Phase 1, 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 28 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Pediatric Brain Tumor Consortium, which has 8 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 7 conditions, with Lymphoma appearing as the primary indexed condition, and to 1 intervention — of which busulfan 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: NCT00006246 reports 8 study locations spanning 7 distinct geographic areas — top geographies include Pennsylvania, California, District of Columbia. 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 NCT00006246 about?

NCT00006246 is a clinical study titled "Busulfan in Treating Children and Adolescents With Refractory CNS Cancer". RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. PURPOSE: Phase I trial to study the safety of delivering intrathecal busulfan in children and adolescents who have refractory CNS cancer and to estimate the maximum tolerated dose...

What is the current status of trial NCT00006246?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 28 participants. The study started on 2000-11.

What conditions does trial NCT00006246 study?

This clinical trial studies the following conditions: Lymphoma, Leukemia, Sarcoma, Metastatic Cancer, Brain and Central Nervous System Tumors. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00006246?

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

Who is sponsoring clinical trial NCT00006246?

This trial is sponsored by Pediatric Brain Tumor Consortium, which has 8 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00006246 being conducted?

This trial has 8 study locations across California, District of Columbia, Massachusetts, North Carolina, Pennsylvania. 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