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Completed Phase 2 Interventional Results available

Comparison of IV Topotecan/Docetaxel to Docetaxel Alone in Second-Line Stage IIIB/IV Non-Small Cell Lung Cancer

ClinicalTrials.gov ID: NCT00065182

Public ClinicalTrials.gov record NCT00065182. 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 Oct 14, 2026, 8:56 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

WEEKLY IV TOPOTECAN/DOCETAXEL COMBINATION COMPARED TO DOCETAXEL IN PATIENTS WITH PRETREATED ADVANCED NSCLC: AN OPEN-LABEL MULTICENTER RANDOMIZED PHASE III TRIAL

Brief summary

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

The purpose of this study is to compare the efficacy and safety of a weekly regimen of two FDA approved drugs in combination versus one FDA approved drug in subjects with advanced non-small cell lung cancer who have received one previous chemotherapy excluding TAXOTERE or HYCAMTIN.

Study identification

NCT ID
NCT00065182
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
399 participants

Conditions and interventions

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
Aug 14, 2003 (Actual)
Primary completion
Aug 30, 2007 (Actual)
Completion
Aug 30, 2007 (Actual)
Last update posted
Jun 24, 2019

2003 – 2007

United States locations

U.S. sites
67
U.S. states
30
U.S. cities
62
Facility City State ZIP Site status
GSK Investigational Site Huntsville Alabama 35801 —
GSK Investigational Site Mobile Alabama 36608 —
GSK Investigational Site Tucson Arizona 85712 —
GSK Investigational Site Little Rock Arkansas 72205 —
GSK Investigational Site Fresno California 93720 —
GSK Investigational Site Los Angeles California 90067 —
GSK Investigational Site Poway California 92064 —
GSK Investigational Site Denver Colorado 80210 —
GSK Investigational Site Washington D.C. District of Columbia 20307-5001 —
GSK Investigational Site Washington D.C. District of Columbia 20422 —
GSK Investigational Site Boca Raton Florida 33428 —
GSK Investigational Site Boca Raton Florida 33486 —
GSK Investigational Site Lakeland Florida 33805 —
GSK Investigational Site Miami Shores Florida 33138 —
GSK Investigational Site Orange Park Florida 32073 —
GSK Investigational Site Orlando Florida 32804 —
GSK Investigational Site Stuart Florida 34994 —
GSK Investigational Site Columbus Georgia 31902 —
GSK Investigational Site Decatur Illinois 62526 —
GSK Investigational Site Elk Grove Village Illinois 60007 —
GSK Investigational Site Skokie Illinois 60077 —
GSK Investigational Site Urbana Illinois 61801 —
GSK Investigational Site Indianapolis Indiana 46202 —
GSK Investigational Site Bowling Green Kentucky 42101 —
GSK Investigational Site Louisville Kentucky 40207 —
GSK Investigational Site Louisville Kentucky 40215 —
GSK Investigational Site Baton Rouge Louisiana 70808 —
GSK Investigational Site Lafayette Louisiana 70506 —
GSK Investigational Site Lake Charles Louisiana 70601 —
GSK Investigational Site Frederick Maryland 21701 —
GSK Investigational Site Boston Massachusetts 02118 —
GSK Investigational Site Grosse Pointe Woods Michigan 48236 —
GSK Investigational Site Minneapolis Minnesota 55407-3799 —
GSK Investigational Site Minneapolis Minnesota 55417 —
GSK Investigational Site Robbinsdale Minnesota 55422 —
GSK Investigational Site Springfield Missouri 65807 —
GSK Investigational Site St Louis Missouri 63141 —
GSK Investigational Site Las Vegas Nevada 89106 —
GSK Investigational Site Reno Nevada 89502 —
GSK Investigational Site Hackensack New Jersey 07601 —
GSK Investigational Site Buffalo New York 14215-1199 —
GSK Investigational Site East Syracuse New York 13057 —
GSK Investigational Site Manhasset New York 11030 —
GSK Investigational Site New Hyde Park New York 11040 —
GSK Investigational Site Nyack New York 10960 —
GSK Investigational Site Rochester New York 14623 —
GSK Investigational Site The Bronx New York 10467 —
GSK Investigational Site Fayetteville North Carolina 28302-2000 —
GSK Investigational Site Winston-Salem North Carolina 27103 —
GSK Investigational Site Canton Ohio 44718 —
GSK Investigational Site Dunmore Pennsylvania 18512 —
GSK Investigational Site Philadelphia Pennsylvania 19114 —
GSK Investigational Site Columbia South Carolina 29203 —
GSK Investigational Site Hilton Head Island South Carolina 29926 —
GSK Investigational Site Spartanburg South Carolina 29303 —
GSK Investigational Site Knoxville Tennessee 37916 —
GSK Investigational Site Nashville Tennessee 37203 —
GSK Investigational Site Irving Texas 75038 —
GSK Investigational Site Tyler Texas 75701 —
GSK Investigational Site Abingdon Virginia 24211 —
GSK Investigational Site Norfolk Virginia 23502 —
GSK Investigational Site Norfolk Virginia 23507 —
GSK Investigational Site Spokane Washington 99204 —
GSK Investigational Site Tacoma Washington 98405 —
GSK Investigational Site Milwaukee Wisconsin 53295 —
GSK Investigational Site Sheboygan Wisconsin 53081 —
GSK Investigational Site Casper Wyoming 85601 —

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 18 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00065182, 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 Jun 24, 2019 · Synced Oct 14, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00065182 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →