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NCT00005952 · ClinicalTrials.gov registry record · Phase 1

Temozolomide Plus Peripheral Stem Cell Transplantation in Treating Children With Newly Diagnosed Malignant Glioma or Recurrent CNS or Other Solid Tumors

A Phase 1 study, sponsored by Duke University.

Completed
Registry status
Phase 1
Development phase
30
Enrollment target

NCT00005952: Completed Phase 1 study, sponsored by Duke University.

NCT00005952 is a Phase 1 study that has completed, run by Duke University. The registered enrollment target is 30 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (50% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00005952, a Phase 1 study, has completed, sponsored by Duke University.

COMPLETED
Registry status
Phase 1
Development phase
30 participants
Enrollment target

Study Summary

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining chemotherapy with peripheral stem cell transplantation may allow the doctor to give higher doses of chemotherapy drugs and kill more tumor cells. PURPOSE: This phase I/II trial is studying the side effects and best dose of temozolomide when given with peripheral stem cell transplantation and to see how well they work in treating children with newly diagnosed malignant glioma or recurrent CNS tumors or other solid tumors.

Interventions

  • DRUG temozolomide
  • PROCEDURE peripheral blood stem cell transplantation
  • BIOLOGICAL filgrastim

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2000-08
Est. Completion 2005-11
Phase Phase 1
Duke University

1,725 total trials

What the finished NCT00005952 record still lists

NCT00005952 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (50% lower).

The record links to 0 conditions, and to 3 interventions - of which temozolomide is the first listed.

NCT00005952 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00005952 about?

NCT00005952 is a clinical study titled "Temozolomide Plus Peripheral Stem Cell Transplantation in Treating Children With Newly Diagnosed Malignant Glioma or Recurrent CNS or Other Solid Tumors". RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining chemotherapy with peripheral stem cell transplantation may allow the doctor to give higher doses of chemotherapy drugs and kill more tumor cells. PURPOSE: This phase I/I...

What is the current status of trial NCT00005952?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 30 participants. The study started on 2000-08. Estimated completion is 2005-11.

What interventions are being tested in trial NCT00005952?

The interventions under investigation include: temozolomide (DRUG), peripheral blood stem cell transplantation (PROCEDURE), filgrastim (BIOLOGICAL).

Who is sponsoring clinical trial NCT00005952?

This trial is sponsored by Duke University, which has 1,725 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00005952's enrollment target sits among peer trials

30 1332nd of 2000 higher than 561 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00005952, the US trial registry maintained by the National Library of Medicine. NCT00005952 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.