Lung Cancer Clinical Trial

MEK Inhibitor PD-325901 To Treat Advanced Non-Small Cell Lung Cancer

Summary

MEK is a critical member of the MAPK pathway involved in growth and survival of cancer cells. PD-325901 is a new drug designed to block this pathway and kill cancer cells. The purpose of this study is to study the effectiveness of PD-325901 in patients with non-small cell lung cancer. PD-325901 will be given by mouth as a pill twice a day, CT scans will be done and biopsies of a tumor and a blood sample will be taken before treatment to examine the how genes affect tumor response to the study medication. Blood samples will be taken to measure the amount of drug in the blood.

View Full Description

Full Description

This study was terminated prematurely on 23 March 2007 due to safety issues (ocular and neurological toxicity observed in another PD-0325901 study, A4581001) as well as lack of objective responses

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Histologically documented non-small cell lung cancer with metastases (Stage IV or recurrent disease) or locally advanced (Stage IIIB) with malignant pleural effusion with no expectation of further effects of prior anticancer therapy, and resolution of all acute toxic effects
Adequate renal, liver, and bone marrow function, determined within 2 weeks prior to the first treatment and an ECOG status of <=1.
Must have evidence of progression of disease within 6 months of most recent prior systemic anticancer therapy.

Exclusion Criteria:

No parathyroid disorder or history of malignancy associated hypercalcemia
No ongoing radiation therapy or radio-cytotoxic therapy within prior 4 weeks; No immunotherapy, biologic therapy, hormonal, or molecular targeted therapy within prior 2 weeks
No concurrent serious infection or life-threatening illness (unrelated to tumor)
No history of a malignancy (other tha non-small cell lung cancer) except those treated with curative intent for skin cancer (other than melanoma) or in situ breast or cervical cancer or those treated with curative intent for any other cancer with no evidence of disease for 5 years.
No active seizure disorders or untreated brain metastases.

Study is for people with:

Lung Cancer

Phase:

Phase 2

Estimated Enrollment:

34

Study ID:

NCT00174369

Recruitment Status:

Terminated

Sponsor:

Pfizer

Check Your Eligibility

Let’s see if you might be eligible for this study.

What is your age and gender ?

Submit

There are 14 Locations for this study

See Locations Near You

Pfizer Investigational Site
Greenbrae California, 94904, United States
Pfizer Investigational Site
La Jolla California, 92093, United States
Pfizer Investigational Site
LaJolla California, 92037, United States
Pfizer Investigational Site
San Diego California, 92103, United States
Pfizer Investigational Site
San Mateo California, 94402, United States
Pfizer Investigational Site
Tampa Florida, 33612, United States
Pfizer Investigational Site
Ann Arbor Michigan, 48106, United States
Pfizer Investigational Site
Detroit Michigan, 48201, United States
Pfizer Investigational Site
Farmington Hills Michigan, 48334, United States
Pfizer Investigational Site
Coon Rapids Minnesota, 55433, United States
Pfizer Investigational Site
Fridley Minnesota, 55432, United States
Pfizer Investigational Site
Robbinsdale Minnesota, 55422, United States
Pfizer Investigational Site
New York New York, 11725, United States
Pfizer Investigational Site
Philadelphia Pennsylvania, 19111, United States

How clear is this clinincal trial information?

Study is for people with:

Lung Cancer

Phase:

Phase 2

Estimated Enrollment:

34

Study ID:

NCT00174369

Recruitment Status:

Terminated

Sponsor:


Pfizer

How clear is this clinincal trial information?

×

Introducing, the Journey Bar

Use this bar to access information about the steps in your cancer journey.

Please confirm you are a US based health care provider:

Yes, I am a health care Provider No, I am not a health care provider