Expired Study
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Anchorage, Alaska


Purpose:

The primary purpose of this study is to estimate the number of patients with non-small cell lung cancer whose tumor responds to the treatments given in this study.


Criteria:

Inclusion Criteria: - Must have advanced or metastatic non-small cell lung cancer that has not been previously treated with any chemotherapy. - Must not have received cetuximab or any medications that target the same pathway as cetuximab (such as Iressa or Tarceva). - Must not have had hypersensitivity or severe allergic reactions to any monoclonal antibodies and must not have severe restrictive or interstitial lung disease. - Must be able to carry out work of light or sedentary nature (e.g. light house work, office work). - It must be at least 4 weeks since last major surgery or prior treatment with an investigational product and at least 12 weeks from any radiation therapy to the chest. Exclusion Criteria: - Women who are pregnant or breastfeeding. - Women with a positive pregnancy test on enrollment or prior to study drug administration. - Any concurrent malignancy (subjects with a previous malignancy but without evidence of disease for 5 years will be allowed to enter the trial). - Symptomatic or uncontrolled metastases in the central nervous system (CNS). - Peripheral neuropathy. - Inadequate hematologic function defined by an absolute neutrophil count (ANC) <1,500/mm^3, a platelet count <100,000/mm^3, or a hemoglobin level < 9g/dL. - Inadequate liver function. - Inadequate kidney function.


NCT ID:

NCT00112346


Primary Contact:

Study Director
Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST)
Eli Lilly and Company


Backup Contact:

N/A


Location Contact:

Anchorage, Alaska
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: November 18, 2019

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