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Terminated Phase 2 Interventional

Trial of Pemetrexed With or Without PF-3512676 in Advanced Non-Small Cell Lung Cancer

ClinicalTrials.gov ID: NCT00321308

Public ClinicalTrials.gov record NCT00321308. 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 5, 2026, 8:56 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 Randomized Phase II Trial Of Pemetrexed With Or Without PF-3512676 For The Treatment Of Patients With Locally Advanced Or Metastatic Non-Small Cell Lung Cancer After Failure Of One Prior Chemotherapy Regimen For Advanced Disease

Brief summary

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

To assess the efficacy and safety of PF-3512676 administered in combination with pemetrexed for the treatment of patients with locally advanced or metastatic NSCLC who have failed one prior chemotherapy regimen

Study identification

NCT ID
NCT00321308
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
36 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
Aug 31, 2006
Primary completion
Dec 31, 2007
Completion
Dec 31, 2007
Last update posted
Sep 27, 2009

2006 – 2008

United States locations

U.S. sites
17
U.S. states
7
U.S. cities
15
Facility City State ZIP Site status
Pfizer Investigational Site Litchfield Park Arizona 85340
Pfizer Investigational Site Sun City Arizona 85351
Pfizer Investigational Site Bentonville Arkansas 72712
Pfizer Investigational Site Fayetteville Arkansas 72703
Pfizer Investigational Site Hudson Florida 34667
Pfizer Investigational Site New Port Richey Florida 34655
Pfizer Investigational Site Mahwah New Jersey 07430
Pfizer Investigational Site Midland Park New Jersey 07432
Pfizer Investigational Site Paramus New Jersey 07652
Pfizer Investigational Site Westwood New Jersey 07675
Pfizer Investigational Site Oneida New York 13421
Pfizer Investigational Site Oswego New York 13126
Pfizer Investigational Site Syracuse New York 13210-2306
Pfizer Investigational Site Syracuse New York 13210
Pfizer Investigational Site Sylvania Ohio 43560
Pfizer Investigational Site Seattle Washington 89109
Pfizer Investigational Site Seattle Washington 98195

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 3 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00321308, 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 Sep 27, 2009 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00321308 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →