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COMPLETED Phase 3

A Study In Patients With Non-Small Cell Lung Cancer To Test If Erlotinib Plus SU011248 Is Better Than Erlotinib Alone

NCT00457392 · View on ClinicalTrials.gov ↗

Study Summary

This study will test whether treatment with erlotinib plus SU011248 is better than erlotinib alone in patients with advanced/metastatic lung cancer who have received previous treatment with a platinum-based regimen.

Interventions

  • DRUG placebo
  • DRUG sunitinib
  • DRUG erlotinib

Study Locations (20)

California

  • Pfizer Investigational Site — Antioch
  • Pfizer Investigational Site — Burbank
  • Pfizer Investigational Site — Downey
  • Pfizer Investigational Site — Fresno
  • Pfizer Investigational Site — La Jolla
  • Pfizer Investigational Site — La Jolla
  • Pfizer Investigational Site — Montebello
  • Pfizer Investigational Site — Pleasant Hill
  • Pfizer Investigational Site — San Diego
  • Pfizer Investigational Site — San Leandro
  • Pfizer Investigational Site — Whittier

Florida

  • Pfizer Investigational Site — Brooksville
  • Pfizer Investigational Site — Cocoa Beach
  • Pfizer Investigational Site — Fort Lauderdale
  • Pfizer Investigational Site — Merritt Island

Alabama

  • Pfizer Investigational Site — Florence
  • Pfizer Investigational Site — Muscle Shoals

Arizona

  • Pfizer Investigational Site — Scottsdale

Arkansas

  • Pfizer Investigational Site — Hot Springs

Connecticut

  • Pfizer Investigational Site — Fairfield

Trial Details

FieldValue
Enrollment Target 960 participants
Start Date 2007-07
Est. Completion 2012-12
Phase Phase 3

Sponsor

Pfizer

769 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00457392

The ClinicalTrials.gov registry entry for NCT00457392 describes a study currently listed as completed. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 960 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Pfizer, which has 769 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Carcinoma, Non-Small Cell Lung appearing as the primary indexed condition, and to 3 interventions — of which placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00457392 reports 20 study locations spanning 6 distinct geographic areas — top geographies include California, Florida, Alabama. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00457392 about?

NCT00457392 is a clinical study titled "A Study In Patients With Non-Small Cell Lung Cancer To Test If Erlotinib Plus SU011248 Is Better Than Erlotinib Alone". This study will test whether treatment with erlotinib plus SU011248 is better than erlotinib alone in patients with advanced/metastatic lung cancer who have received previous treatment with a platinum-based regimen.

What is the current status of trial NCT00457392?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 960 participants. The study started on 2007-07. Estimated completion is 2012-12.

What conditions does trial NCT00457392 study?

This clinical trial studies the following conditions: Carcinoma, Non-Small Cell Lung. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00457392?

The interventions under investigation include: placebo (DRUG), sunitinib (DRUG), erlotinib (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00457392?

This trial is sponsored by Pfizer, which has 769 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00457392 being conducted?

This trial has 20 study locations across Alabama, Arizona, Arkansas, California, Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial