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Completed Phase 2 Interventional

The Study Of An Oral Drug Called A Radiation Sensitizer In Patients With Newly Diagnosed Small Cell Lung Cancer (SCLC)

ClinicalTrials.gov ID: NCT00043862

Public ClinicalTrials.gov record NCT00043862. 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 Jun 25, 2026, 4:09 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

A Phase II Trial of Twice Daily Oral Topotecan as a Radiation Sensitizer With Twice Daily Radiotherapy for Newly Diagnosed Small Cell Lung Cancer

Study identification

NCT ID
NCT00043862
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
60 participants

Conditions and interventions

Interventions

  • topotecan Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
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
Jul 31, 2002
Primary completion
Oct 31, 2005
Completion
Not listed
Last update posted
May 30, 2017

Started 2002

United States locations

U.S. sites
31
U.S. states
17
U.S. cities
30
Facility City State ZIP Site status
GSK Investigational Site Phoenix Arizona 85013 - 4496
GSK Investigational Site Little Rock Arkansas 72205
GSK Investigational Site Bakersfield California 93309
GSK Investigational Site Fountain Valley California 92708
GSK Investigational Site Los Angeles California 90057
GSK Investigational Site Gainesville Florida 32610
GSK Investigational Site Indianapolis Indiana 46260
GSK Investigational Site Lexington Kentucky 40536-0098
GSK Investigational Site New Orleans Louisiana 70112
GSK Investigational Site New Orleans Louisiana 70121
GSK Investigational Site Shreveport Louisiana 71103
GSK Investigational Site Scarborough Maine 04074
GSK Investigational Site Springfield Massachusetts 01107
GSK Investigational Site Duluth Minnesota 55805
GSK Investigational Site Minneapolis Minnesota 55455
GSK Investigational Site Robbinsdale Minnesota 55422
GSK Investigational Site St Louis Missouri 63141
GSK Investigational Site Saint Louis Montana 63110
GSK Investigational Site Albuquerque New Mexico 87109
GSK Investigational Site Raleigh North Carolina 27609
GSK Investigational Site Akron Ohio 44304
GSK Investigational Site Cincinnati Ohio 45236
GSK Investigational Site Cleveland Ohio 44106
GSK Investigational Site Toledo Ohio 43614-5809
GSK Investigational Site Fort Worth Texas 76104
GSK Investigational Site San Antonio Texas 78229
GSK Investigational Site Green Bay Wisconsin 54301
GSK Investigational Site La Crosse Wisconsin 54601
GSK Investigational Site Madison Wisconsin 53792
GSK Investigational Site Milwaukee Wisconsin 53215
GSK Investigational Site Wausau Wisconsin 54401

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00043862, 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 May 30, 2017 · Synced Jun 25, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00043862 live on ClinicalTrials.gov.

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