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Completed Phase 1Phase 2 Interventional

A Clinical Efficacy Study Of An Oral Tyrosine Kinase Inhibitor Of VEGFR-2 Given In Combination With Chemotherapy

ClinicalTrials.gov ID: NCT00074854

Public ClinicalTrials.gov record NCT00074854. 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 3, 2026, 1:03 AM 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 Clinical Efficacy Study Of An Oral Tyrosine Kinase Inhibitor Of VEGFR-2 Given In Combination With Chemotherapy (Paclitaxel And Carboplatin) Vs. Chemotherapy Alone For The Treatment Of Advanced Stage Non-Small Cell Lung Cancer.

Brief summary

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

The purpose of this study is to determine whether CP-547,632, an oral VEGFR-2 tyrosine kinase inhibitor when given in combination with chemotherapy (carboplatin and paclitaxel) is effective in the treatment of advanced stage non-small cell lung cancer.

Study identification

NCT ID
NCT00074854
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
87 participants

Conditions and interventions

Conditions

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
Apr 30, 2002
Primary completion
Not listed
Completion
Feb 28, 2005
Last update posted
Nov 8, 2006

2002 – 2005

United States locations

U.S. sites
20
U.S. states
7
U.S. cities
16
Facility City State ZIP Site status
Pfizer Investigational Site Greenbrae California 94904
Pfizer Investigational Site San Mateo California 94402
Pfizer Investigational Site San Pablo California 94806
Pfizer Investigational Site Tampa Florida 33612-9497
Pfizer Investigational Site Covington Louisiana 70433
Pfizer Investigational Site Metairie Louisiana 70002
Pfizer Investigational Site Metairie Louisiana 70006
Pfizer Investigational Site New Orleans Louisiana 70115
Pfizer Investigational Site Boston Massachusetts 02215
Pfizer Investigational Site Stony Brook New York 11794
Pfizer Investigational Site Philadelphia Pennsylvania 19111
Pfizer Investigational Site Gallatin Tennessee 37066
Pfizer Investigational Site Hermitage Tennessee 37076
Pfizer Investigational Site Lebanon Tennessee 37087
Pfizer Investigational Site Murfreesboro Tennessee 37130
Pfizer Investigational Site Nashville Tennessee 37203
Pfizer Investigational Site Nashville Tennessee 37205
Pfizer Investigational Site Nashville Tennessee 37207
Pfizer Investigational Site Nashville Tennessee 37211
Pfizer Investigational Site Smyrna Tennessee 37167

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 NCT00074854, 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 Nov 8, 2006 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00074854 live on ClinicalTrials.gov.

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