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

NCT00354913 · ClinicalTrials.gov registry record · Phase 2

Imatinib Mesylate and Hydroxyurea in Treating Patients With Recurrent or Progressive Meningioma

A Phase 2 study, sponsored by Duke University.

Completed
Registry status
Phase 2
Development phase
21
Enrollment target

NCT00354913: Completed Phase 2 study, sponsored by Duke University.

NCT00354913 is a Phase 2 study that has completed, run by Duke University. The registered enrollment target is 21 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (84% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00354913, a Phase 2 study, has completed, sponsored by Duke University.

COMPLETED
Registry status
Phase 2
Development phase
21 participants
Enrollment target

Study Summary

RATIONALE: Imatinib mesylate may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as hydroxyurea, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving imatinib mesylate together with hydroxyurea may kill more tumor cells. PURPOSE: This phase II trial is studying how well giving imatinib mesylate together with hydroxyurea works in treating patients with recurrent or progressive meningioma.

Primary Outcome

Percentage of participants surviving six months from the start of study treatment without progression of disease. PFS was defined as the time from the date of study treatment initiation to the date of the first documented progression according to the Macdonald criteria, or death due to any cause.

Interventions

  • DRUG imatinib mesylate
  • DRUG hydroxyurea

Trial Details

FieldValue
Enrollment Target 21 participants
Start Date 2005-05
Est. Completion 2010-10
Phase Phase 2
Duke University

1,725 total trials

What the finished NCT00354913 record still lists

NCT00354913 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 21 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (84% lower).

The record links to 0 conditions, and to 2 interventions - of which imatinib mesylate is the first listed.

NCT00354913 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00354913 about?

NCT00354913 is a clinical study titled "Imatinib Mesylate and Hydroxyurea in Treating Patients With Recurrent or Progressive Meningioma". RATIONALE: Imatinib mesylate may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as hydroxyurea, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving ima...

What is the current status of trial NCT00354913?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 21 participants. The study started on 2005-05. Estimated completion is 2010-10.

What interventions are being tested in trial NCT00354913?

The interventions under investigation include: imatinib mesylate (DRUG), hydroxyurea (DRUG).

Who is sponsoring clinical trial NCT00354913?

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 NCT00354913's enrollment target sits among peer trials

21 1794th of 2000 higher than 196 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 enrollment target

  • NCT02447874 · 21 participants · Phase 1

    Arginine Therapy for the Treatment of Pain in Children With Sickle Cell Disease

  • NCT03826992 · 21 participants · Phase 1

    Venetoclax Combined With Vyxeos (CPX-351) for Participants With Relapsed or Refractory Acute Leukemia

  • NCT04107077 · 21 participants · Phase 2

    Phase II Study of the Effects of Laparoscopic Hyperthermic Intraperitoneal Chemotherapy (HIPEC) in Patients With Advanced Gastric Cancer

  • NCT04158635 · 21 participants · Phase 1

    Gemcitabine, Nab-Paclitaxel, and Bosentan for the Treatment of Unresectable Pancreatic Cancer

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 NCT00354913, the US trial registry maintained by the National Library of Medicine. NCT00354913 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.