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Completed Phase 3 Interventional

Iressa Versus Docetaxel (Taxotere)

ClinicalTrials.gov ID: NCT00076388

Public ClinicalTrials.gov record NCT00076388. 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 8, 2026, 4:27 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 Randomized, Open-Label, Parallel Group, International, Multicenter, Phase III Study of Oral ZD1839 (IRESSA®) Versus Intravenous Docetaxel (TAXOTERE®) in Patients With Locally Advanced or Metastatic Recurrent Non-Small Cell Lung Cancer Who Have Previously Received Platinum-Based Chemotherapy

Brief summary

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

The purpose of this study is to compare the effects of ZD1839 or docetaxel in patients with advanced non-small cell lung cancer (NSCLC) that has recurred or progressed after receiving prior treatment with platinum-based chemotherapy.

Study identification

NCT ID
NCT00076388
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
AstraZeneca
Industry
Enrollment
1,440 participants

Conditions and interventions

Interventions

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
Jan 31, 2004
Primary completion
Feb 28, 2007
Completion
Sep 30, 2007
Last update posted
May 12, 2011

2004 – 2007

United States locations

U.S. sites
35
U.S. states
22
U.S. cities
35
Facility City State ZIP Site status
Research Site Birmingham Alabama
Research Site Fountain Valley California
Research Site Los Angeles California 90048
Research Site Santa Rosa California
Research Site Stockton California 95204
Research Site Colorado Springs Colorado
Research Site Norwich Connecticut
Research Site Newark Delaware
Research Site Boca Raton Florida
Research Site Orlando Florida 32806
Research Site Macon Georgia
Research Site Tucker Georgia
Research Site Skokie Illinois 60077
Research Site Knoxville Kentucky
Research Site Saint Louis Park Minnesota
Research Site Great Neck New York 11021
Research Site Rochester New York 14621
Research Site Syracuse New York 13210
Research Site Chapel Hill North Carolina 27599
Research Site Charlotte North Carolina
Research Site Durham North Carolina 27710
Research Site Cleveland Ohio 44195
Research Site Portland Oregon
Research Site Philadelphia Pennsylvania
Research Site Pittsburgh Pennsylvania
Research Site Columbia South Carolina
Research Site Nashville Tennessee
Research Site Austin Texas
Research Site Dallas Texas
Research Site Houston Texas 77030-4009
Research Site Tyler Texas
Research Site Salt Lake City Utah
Research Site Fairfax Virginia
Research Site Seattle Washington
Research Site Racine Wisconsin

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 127 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00076388, 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 12, 2011 · Synced Sep 8, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00076388 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →