Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 1Phase 2 Interventional Results available

Evaluation Of The Efficacy Of The Combination Of Axitinib With Pemetrexed And Cisplatin In The Treatment Of Non-Squamous Non-Small Cell Lung Cancer

ClinicalTrials.gov ID: NCT00768755

Public ClinicalTrials.gov record NCT00768755. 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, 5:44 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

Randomized Phase 2 Study Of Cisplatin/Pemetrexed With Or Without Axitinib (AG-013736) As First-Line Treatment For Patients With Non-Squamous Non-Small Cell Lung Cancer

Brief summary

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

AG-013736 (axitinib) in combination with cisplatin and pemetrexed will be evaluated as first-line treatment of patients with locally advanced, recurrent, or metastatic non-squamous, non small cell lung cancer (NSCLC).

Study identification

NCT ID
NCT00768755
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
180 participants

Conditions and interventions

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
Dec 31, 2008
Primary completion
Feb 28, 2011
Completion
Feb 29, 2012
Last update posted
Oct 27, 2015

2009 – 2012

United States locations

U.S. sites
12
U.S. states
5
U.S. cities
11
Facility City State ZIP Site status
Pfizer Investigational Site Huntsville Alabama 35805
Pfizer Investigational Site Atlanta Georgia 30341
Pfizer Investigational Site Decatur Georgia 30033
Pfizer Investigational Site Macon Georgia 31217
Pfizer Investigational Site Marietta Georgia 30060
Pfizer Investigational Site Sandy Springs Georgia 30342
Pfizer Investigational Site Bloomington Illinois 61701
Pfizer Investigational Site Peoria Illinois 61615
Pfizer Investigational Site Hershey Pennsylvania 17033-0850
Pfizer Investigational Site West Reading Pennsylvania 19611
Pfizer Investigational Site East Providence Rhode Island 02914
Pfizer Investigational Site East Providence Rhode Island 02915

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 40 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00768755, 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 27, 2015 · Synced Sep 5, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00768755 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →