Lung Cancer Clinical Trial
Erlotinib Is Being Studied With Or Without An Investigational Drug, PF-02341066, In Patients With Lung Cancer
Summary
This is a Phase 1/2 study comparing the safety and anti-tumor activity of erlotinib alone versus erlotinib in combination with PF-02341066 in patients with advanced non-small cell lung cancer.
Eligibility Criteria
Inclusion Criteria:
histologically proven diagnosis of Non-Small Cell Lung Cancer (NSCLC) that is locally advanced or metastatic and of the adenocarcinoma subtype (including mixed adenosquamous histology)
evident disease progression by Response Evaluation Criterion in Solid Tumors (RECIST) after at least one but no more than 2 chemotherapy regimens for advanced disease
tumors must have measurable disease as per RECIST
Exclusion Criteria:
known interstitial lung disease
prior treatment with an agent that is known or proposed to be active by action on EGFR tyrosine kinase or c-Met/HGF (Phase 2 Portion)
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There are 13 Locations for this study
Birmingham Alabama, 35233, United States
Birmingham Alabama, 35294, United States
Orange California, 92868, United States
Orange California, 92868, United States
Orange California, 92868, United States
Fort Lauderdale Florida, 33308, United States
Creve Coeur Missouri, 63141, United States
St. Louis Missouri, 63110, United States
St. Louis Missouri, 63110, United States
St. Peters Missouri, 63376, United States
Columbus Ohio, 43205, United States
Columbus Ohio, 43210, United States
Columbus Ohio, 43221, United States
San Antonio Texas, 78229, United States
Seattle Washington, 98109, United States
Seattle Washington, 98195, United States
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