A Study of Cetuximab in Patients Who Have Stage IV Colorectal Cancer

Completed · Phase 2

Conditions studied: Colorectal Neoplasms

In brief

The purpose of this clinical research study is to learn about the safety of cetuximab in patients with stage IV colorectal cancer, and who may benefit from cetuximab.

Key facts

Study ID: NCT00055419
Run by: Eli Lilly and Company
People needed: 744
Starts: 2003-02-01
Expected to finish: 2004-08-01
Last updated by the study team: 2010-04-09

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Subjects must have signed an approved informed consent prior to any study procedures.
Subjects with histologically or pathologically confirmed metastatic colorectal cancer, which is EGFR-positive by IHC (may be based on archival samples)
Subjects with ECOG performance status 0, 1 or 2.
Subjects who have failed, either due to lack of efficacy or due to intolerance, all available chemotherapy for the treatment of metastatic colorectal cancer.
Subjects who have failed to meet eligibility criteria for any other existing cetuximab trial.
Subjects must have received at least two chemotherapy regimens for metastatic disease OR adjuvant therapy plus one chemotherapy regimen for metastatic disease, provided the subject progressed within 6 months of completing their adjuvant therapy.
Prior chemotherapy must have included all of the follow drugs: irinotecan, oxaliplatin, and a fluoropyrimidine.
Subjects adequately recovered from any recent surgery, radiation therapy or chemotherapy.
Subjects accessible for treatment and follow-up. Subjects enrolled in this trial must be treated at the participating center.
Subjects greater or equal to 18 years of age.
Women of childbearing potential must be using an adequate method of contraception to avoid pregnancy throughout the study and for up to 4 weeks afterwards.

You may not qualify if…

Women of childbearing potential who are unwilling or unable to use an acceptable method to avoid pregnancy for the entire study period and for up to 4 weeks after the study.
Women who are pregnant or breastfeeding.
Women with a positive pregnancy test on enrollment or prior to study drug administration.
Sexually active, fertile men not using adequate birth control.
Subjects with dementia, altered mental status, or any psychiatric condition that would prohibit the understanding or rendering of informed consent.
Subjects with a serious uncontrolled medical disorder that would impair the ability of the patient to receive protocol therapy.
Subjects with a history of uncontrolled angina, arrhythmias, congestive heart failure, or myocardial infarction within the previous 6 months.
Subjects with any concurrent malignancy other than non-melanoma skin cancer, or carcinoma in situ of the cervix. Subjects with a previous malignancy but without evidence of disease for > 5 years will be allowed to enter the trial.
Subjects with any history of severe hypersensitivity reactions and/or anaphylaxis resulting from the administration of protein based therapeutic agents.
Subjects with inadequate hematologic function defined by an absolute neutrophil count (ANC) <1,250/mm3, a platelet count <75,000/mm3, and a hemoglobin level <8 g/dL.
Subjects with inadequate hepatic function, defined by a total bilirubin level ³3 times the upper limit of normal (ULN) and an aspartate transaminase (AST) and alanine transaminase (ALT) levels >5 x ULN.
Subjects with inadequate renal function defined by a serum creatinine level >2.5 x ULN.
Prior cetuximab therapy, prior randomization on a study which includes cetuximab therapy in a treatment arm, or any other prior therapy that targets the EGFR pathway.
A history of prior therapy with a chimerized or murine monoclonal antibody.
Prisoners or subjects who are compulsorily detained (involuntarily incarcerated) for treatment of either a psychiatric or physical (e.g., infectious disease) illness must not be enrolled into this study.
A history of cetuximab or therapy that targeted the EGFR receptor.
A history of prior anti-cancer murine monoclonal antibody therapy.
Additional concurrent chemotherapy or other investigational anticancer agents may not be administered to subjects on this study.

Where it is running

ImClone Investigational Site — Bakersfield, California, United States
ImClone Investigational Site — Los Angeles, California, United States
ImClone Investigational Site — Denver, Colorado, United States
ImClone Investigational Site — Torrington, Connecticut, United States
ImClone Investigational Site — Washington D.C., District of Columbia, United States
ImClone Investigational Site — Jacksonville, Florida, United States
ImClone Investigational Site — Miami, Florida, United States
ImClone Investigational Site — Orlando, Florida, United States
ImClone Investigational Site — Atlanta, Georgia, United States
ImClone Investigational Site — Decatur, Illinois, United States
ImClone Investigational Site — Louisville, Kentucky, United States
ImClone Investigational Site — New Orleans, Louisiana, United States
ImClone Investigational Site — Baltimore, Maryland, United States
ImClone Investigational Site — Ypsilanti, Michigan, United States
ImClone Investigational Site — Minneapolis, Minnesota, United States
ImClone Investigational Site — Saint Charles, Missouri, United States
ImClone Investigational Site — Great Falls, Montana, United States
ImClone Investigational Site — Las Vegas, Nevada, United States
ImClone Investigational Site — Voorhees Township, New Jersey, United States
ImClone Investigational Site — East Setauket, New York, United States
ImClone Investigational Site — Latham, New York, United States
ImClone Investigational Site — New York, New York, United States
ImClone Investigational Site — Cleveland, Ohio, United States
ImClone Investigational Site — Portland, Oregon, United States
ImClone Investigational Site — Greenville, South Carolina, United States

Full record on ClinicalTrials.gov

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