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

NCT00378911 · ClinicalTrials.gov registry record · Phase 2

Sunitinib in Treating Patients With Recurrent or Persistent Leiomyosarcoma of the Uterus

A Phase 2 study of Uterine Leiomyosarcoma and Recurrent Uterine Sarcoma, sponsored by National Cancer Institute (NCI).

Completed
Registry status
Phase 2
Development phase
44
Enrollment target
1
Study location

NCT00378911: Completed Phase 2 study of Uterine Leiomyosarcoma and Recurrent Uterine Sarcoma, sponsored by National Cancer Institute (NCI).

NCT00378911 is a Phase 2 study of Uterine Leiomyosarcoma and Recurrent Uterine Sarcoma that has completed, run by National Cancer Institute (NCI). The registered enrollment target is 44 participants, above the 35-participant average among 3 other Uterine Leiomyosarcoma trials with a reported enrollment target (26% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00378911, a Phase 2 study of Uterine Leiomyosarcoma and Recurrent Uterine Sarcoma, has completed, sponsored by National Cancer Institute (NCI).

COMPLETED
Registry status
Phase 2
Development phase
44 participants
Enrollment target
1
Study location

Study Summary

This phase II trial is studying how well sunitinib works in treating patients with recurrent or persistent leiomyosarcoma of the uterus. Sunitinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor.

Interventions

  • DRUG sunitinib malate

Study Locations (1)

Pennsylvania

  • Gynecologic Oncology Group - Philadelphia

Trial Details

FieldValue
Enrollment Target 44 participants
Start Date 2006-10
Est. Completion 2010-01
Phase Phase 2
National Cancer Institute (NCI)

3,257 total trials

What the finished NCT00378911 record still lists

NCT00378911 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 44 participants, a relatively small participant target, above the 35-participant average among 3 other Uterine Leiomyosarcoma trials with a reported enrollment target (26% higher).

The record links to 2 conditions, with Uterine Leiomyosarcoma appearing as the primary indexed condition, and to 1 intervention - of which sunitinib malate is the first listed.

NCT00378911 reports a single indexed study location in Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT00378911 about?

NCT00378911 is a clinical study titled "Sunitinib in Treating Patients With Recurrent or Persistent Leiomyosarcoma of the Uterus". This phase II trial is studying how well sunitinib works in treating patients with recurrent or persistent leiomyosarcoma of the uterus. Sunitinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor.

What is the current status of trial NCT00378911?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 44 participants. The study started on 2006-10. Estimated completion is 2010-01.

What conditions does trial NCT00378911 study?

This clinical trial studies the following conditions: Uterine Leiomyosarcoma, Recurrent Uterine Sarcoma.

What interventions are being tested in trial NCT00378911?

The interventions under investigation include: sunitinib malate (DRUG).

Who is sponsoring clinical trial NCT00378911?

This trial is sponsored by National Cancer Institute (NCI), which has 3,257 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00378911 being conducted?

This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Uterine Leiomyosarcoma

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

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

  • NCT02323945 · 44 participants · NA

    Effects of Breathing Mild Bouts of Low Oxygen on Limb Mobility After Spinal Injury

  • NCT03093909 · 44 participants · Phase 1

    Study of Aerosol Gemcitabine in Patients With Solid Tumors and Pulmonary Metastases

  • NCT03104491 · 44 participants · Phase 1

    Inotuzumab Ozogamicin Post-Transplant For Acute Lymphocytic Leukemia

  • NCT03781765 · 44 participants · Phase 4

    Stimulant vs. Non-stimulant Treatments and Reward Processing in Drug-naive Youth at SUD Risk

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 NCT00378911, the US trial registry maintained by the National Library of Medicine. NCT00378911 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.