Lung Cancer Clinical Trial
A Clinical Efficacy Study Of An Oral Tyrosine Kinase Inhibitor Of VEGFR-2 Given In Combination With Chemotherapy
Summary
The purpose of this study is to determine whether CP-547,632, an oral VEGFR-2 tyrosine kinase inhibitor when given in combination with chemotherapy (carboplatin and paclitaxel) is effective in the treatment of advanced stage non-small cell lung cancer.
Eligibility Criteria
Inclusion Criteria:
Histologically or cytologically confirmed stage IIIB (inicluding those with pleural effusion), IV or recurrent non-small cell lung cancer (nsclc).
Bidimensionally measurable disease >2cm x 1 cm by conventional CT Scan or >1 cm x 1cm by spiral CT Scan.
Exclusion Criteria:
No tumors in close proximity to major veins or arteries.
No sanguinous pleural effusion due to disease or pericardial effusion suspicious for disease.
No evidence or history brain metastases.
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There are 20 Locations for this study
Greenbrae California, 94904, United States
San Mateo California, 94402, United States
San Pablo California, 94806, United States
Tampa Florida, 33612, United States
Covington Louisiana, 70433, United States
Metairie Louisiana, 70002, United States
Metairie Louisiana, 70006, United States
New Orleans Louisiana, 70115, United States
Boston Massachusetts, 02215, United States
Stony Brook New York, 11794, United States
Philadelphia Pennsylvania, 19111, United States
Gallatin Tennessee, 37066, United States
Hermitage Tennessee, 37076, United States
Lebanon Tennessee, 37087, United States
Murfreesboro Tennessee, 37130, United States
Nashville Tennessee, 37203, United States
Nashville Tennessee, 37205, United States
Nashville Tennessee, 37207, United States
Nashville Tennessee, 37211, United States
Smyrna Tennessee, 37167, United States
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