Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00629187 · ClinicalTrials.gov registry record · Phase 1

Safety Study of High Dose Temozolomide to Treat Relapsed/Refractory Central Nervous System (CNS) Malignancy

A Phase 1 study, sponsored by Tufts Medical Center.

Terminated
Registry status
Phase 1
Development phase
2
Enrollment target

NCT00629187: Clinical Trial Phase 1 study, sponsored by Tufts Medical Center.

NCT00629187 is a Phase 1 study that was terminated before completion, run by Tufts Medical Center. The registered enrollment target is 2 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00629187, a Phase 1 study, was terminated before completion, sponsored by Tufts Medical Center.

TERMINATED
Registry status
Phase 1
Development phase
2 participants
Enrollment target

Study Summary

The goal of this study is to find the maximum dose of a drug, temozolomide, that can safely be given to subjects with brain tumors. Past studies showed that the maximum dose of temozolomide was limited by low blood counts. The investigators will use blood stem cells collected from bone marrow to help subjects recover their blood counts, a procedure called autologous stem cell transplant or stem cell rescue. This way, the investigators expect to be able to safely deliver very high doses of temozolomide. This study is only available at Tufts Medical Center.

Interventions

  • DRUG Temozolomide

Trial Details

FieldValue
Enrollment Target 2 participants
Start Date 2004-04
Est. Completion 2012-04
Phase Phase 1
Tufts Medical Center

169 total trials

Why NCT00629187 stopped before completion

NCT00629187 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 2 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (97% lower).

The record links to 0 conditions, and to 1 intervention - of which Temozolomide is the first listed.

NCT00629187 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00629187 about?

NCT00629187 is a clinical study titled "Safety Study of High Dose Temozolomide to Treat Relapsed/Refractory Central Nervous System (CNS) Malignancy". The goal of this study is to find the maximum dose of a drug, temozolomide, that can safely be given to subjects with brain tumors. Past studies showed that the maximum dose of temozolomide was limited by low blood counts. The investigators will use blood stem cells collected from bone marrow to hel...

What is the current status of trial NCT00629187?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 2 participants. The study started on 2004-04. Estimated completion is 2012-04.

What interventions are being tested in trial NCT00629187?

The interventions under investigation include: Temozolomide (DRUG).

Who is sponsoring clinical trial NCT00629187?

This trial is sponsored by Tufts Medical Center, which has 169 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00629187's enrollment target sits among peer trials

2 2000th of 2000 the lowest 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00629187, the US trial registry maintained by the National Library of Medicine. NCT00629187 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.