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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 Oct 27, 2026, 4:12 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 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
Feb 2005 (Type not available)
Primary completion
Aug 2011 (Actual)
Completion
Aug 2011 (Actual)
Last update posted
Oct 30, 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 30, 2013 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00147537 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →