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Completed Phase 1Phase 2 Interventional Results available

Combination Study Of CP-751,871 With Paclitaxel And Carboplatin In Advanced Lung Cancer

ClinicalTrials.gov ID: NCT00147537

Public ClinicalTrials.gov record NCT00147537. 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 10, 2026, 8:02 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 Phase 1b Dose Escalation/Phase 2 Randomized, Non-Comparative, Multiple Center, Open Label Study Of CP 751,871 In Combination With Paclitaxel And Carboplatin And Of Paclitaxel And Carboplatin Alone As First Line Treatment For Advanced Non-Small Cell Lung Cancer

Brief summary

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

Phase 1b Dose Excalation/Expansion: Identify and characterize safety and tolerability of recommended phase 2 dose of CP-751,871 when administered with paclitaxel and carboplatin Phase 1b Erlotinib Extension: To characterize the safety and tolerability of CP751,871 when administered with paclitaxel, carboplatin and erlotinib. Phase 2: To test the efficacy of CP-751,871 combined with paclitaxel and carboplatin in the treatment of advanced non-small cell lung cancer

Study identification

NCT ID
NCT00147537
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
282 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
Jan 31, 2005
Primary completion
Jul 31, 2011
Completion
Jul 31, 2011
Last update posted
Oct 29, 2013

2005 – 2011

United States locations

U.S. sites
26
U.S. states
13
U.S. cities
18
Facility City State ZIP Site status
Pfizer Investigational Site Tucson Arizona 85719
Pfizer Investigational Site Tucson Arizona 85724-5024
Pfizer Investigational Site Tucson Arizona 85724
Pfizer Investigational Site Greenbrae California 94904
Pfizer Investigational Site Los Angeles California 90048
Pfizer Investigational Site Jacksonville Florida 32216
Pfizer Investigational Site Jacksonville Florida 32224
Pfizer Investigational Site Jeffersonville Indiana 47130
Pfizer Investigational Site Louisville Kentucky 40202
Pfizer Investigational Site Louisville Kentucky 40207
Pfizer Investigational Site Louisville Kentucky 40217
Pfizer Investigational Site Louisville Kentucky 40241
Pfizer Investigational Site Shelbyville Kentucky 40065
Pfizer Investigational Site Baltimore Maryland 21204
Pfizer Investigational Site Rochester Minnesota 55905
Pfizer Investigational Site Corinth Mississippi 38834
Pfizer Investigational Site Southaven Mississippi 38671
Pfizer Investigational Site City of Saint Peters Missouri 63376
Pfizer Investigational Site Creve Coeur Missouri 63141
Pfizer Investigational Site St Louis Missouri 63110
Pfizer Investigational Site The Bronx New York 10461
Pfizer Investigational Site The Bronx New York 10467
Pfizer Investigational Site Philadelphia Pennsylvania 19111
Pfizer Investigational Site Memphis Tennessee 38104
Pfizer Investigational Site Memphis Tennessee 38120
Pfizer Investigational Site Houston Texas 77030

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 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00147537, 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 Oct 29, 2013 · Synced Sep 10, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00147537 live on ClinicalTrials.gov.

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