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Completed Phase 2 Interventional Results available

Intravenous Weekly Topotecan In Subjects With Recurrent Or Persistent Endometrial Cancer

ClinicalTrials.gov ID: NCT00267488

Public ClinicalTrials.gov record NCT00267488. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 2:43 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

An Open-label, Phase II, Multicenter Study of Intravenous Weekly Topotecan in Subjects With Recurrent or Persistent Endometrial Cancer

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to find out if Hycamtin given weekly is safe and effective for treating your endometrial cancer.

Study identification

NCT ID
NCT00267488
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
70 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 30, 2005
Primary completion
Nov 30, 2007
Completion
Nov 30, 2007
Last update posted
Jul 10, 2012

2005 – 2007

United States locations

U.S. sites
19
U.S. states
11
U.S. cities
19
Facility City State ZIP Site status
GSK Investigational Site La Jolla California 92037
GSK Investigational Site Los Angeles California 90033
GSK Investigational Site Newport Beach California 92663
GSK Investigational Site Engelwood Colorado 80113
GSK Investigational Site Coral Gables Florida 33146
GSK Investigational Site Lakeland Florida 33805
GSK Investigational Site Miami Florida 33143
GSK Investigational Site Orlando Florida 32804
GSK Investigational Site Atlanta Georgia 30342
GSK Investigational Site Chicago Illinois 60612
GSK Investigational Site Hinsdale Illinois 60521
GSK Investigational Site New Orleans Louisiana 70115
GSK Investigational Site Minneapolis Minnesota 55455
GSK Investigational Site Lincoln Nebraska 68510
GSK Investigational Site Columbia South Carolina 29210
GSK Investigational Site Greenville South Carolina 29605
GSK Investigational Site Chattanooga Tennessee 37403
GSK Investigational Site Knoxville Tennessee 37917
GSK Investigational Site Seattle Washington 98104

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00267488, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 10, 2012 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00267488 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →