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NCT00005031 · ClinicalTrials.gov registry record · Phase 2

Irofulven in Treating Patients With Persistent or Recurrent, Refractory Endometrial Cancer

A Phase 2 study of Endometrial Cancer, sponsored by Gynecologic Oncology Group.

Completed
Registry status
Phase 2
Development phase
20
Study locations

NCT00005031: Completed Phase 2 study of Endometrial Cancer, sponsored by Gynecologic Oncology Group.

NCT00005031 is a Phase 2 study of Endometrial Cancer that has completed, run by Gynecologic Oncology Group. The trial reports 20 study locations across 15 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00005031, a Phase 2 study of Endometrial Cancer, has completed, sponsored by Gynecologic Oncology Group.

COMPLETED
Registry status
Phase 2
Development phase
20
Study locations

Study Summary

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. PURPOSE: Phase II trial to study the effectiveness of irofulven in treating patients who have persistent or recurrent refractory endometrial cancer.

Conditions Studied

Interventions

  • DRUG irofulven

Study Locations (20)

California

  • Community Hospital of Los Gatos - Los Gatos
  • Chao Family Comprehensive Cancer Center - Orange

Illinois

  • Rush-Presbyterian-St. Luke's Medical Center - Chicago
  • University of Chicago Cancer Research Center - Chicago

Massachusetts

  • Tufts University School of Medicine - Boston
  • University of Massachusetts Memorial Medical Center - Worcester

Missouri

  • Ellis Fischel Cancer Center - Columbia
  • Washington University School of Medicine - St Louis

New York

  • Cancer Center of Albany Medical Center - Albany
  • University of Rochester Cancer Center - Rochester

Alabama

  • University of Alabama at Birmingham Comprehensive Cancer Center - Birmingham

District of Columbia

  • Walter Reed Army Medical Center - Washington D.C.

Florida

  • H. Lee Moffitt Cancer Center and Research Institute - Tampa

Trial Details

FieldValue
Start Date 2000-08
Phase Phase 2
Gynecologic Oncology Group

154 total trials

What the finished NCT00005031 record still lists

NCT00005031 is an interventional study that assigns participants to a tested intervention. An enrollment target was not published in the registry record, which is common for early-stage or observational entries.

The record links to 1 condition, with Endometrial Cancer appearing as the primary indexed condition, and to 1 intervention - of which irofulven is the first listed.

NCT00005031 names 20 study sites across 15 states, led by California, Illinois, Massachusetts.

Frequently Asked Questions

What is clinical trial NCT00005031 about?

NCT00005031 is a clinical study titled "Irofulven in Treating Patients With Persistent or Recurrent, Refractory Endometrial Cancer". RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. PURPOSE: Phase II trial to study the effectiveness of irofulven in treating patients who have persistent or recurrent refractory endometrial cancer.

What is the current status of trial NCT00005031?

This trial is currently completed. It is a Phase 2 study. The study started on 2000-08.

What conditions does trial NCT00005031 study?

This clinical trial studies the following conditions: Endometrial Cancer.

What interventions are being tested in trial NCT00005031?

The interventions under investigation include: irofulven (DRUG).

Who is sponsoring clinical trial NCT00005031?

This trial is sponsored by Gynecologic Oncology Group, which has 154 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00005031 being conducted?

This trial has 20 study locations across Alabama, California, District of Columbia, Florida, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT00005031, the US trial registry maintained by the National Library of Medicine. NCT00005031 (unsized enrollment · wide site footprint · completed) retrieved and formatted by PlainTrial, see methodology.