A Phase 2 interventional study of cetuximab and fluorouracil in Colorectal Cancer, sponsored by Institut du Cancer de Montpellier - Val d'Aurelle. Completed at 1 site in France. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2026-02-05.
Sponsored by Institut du Cancer de Montpellier - Val d'Aurelle · Phase 2, Interventional, and Treatment
RATIONALE: Monoclonal antibodies, such as cetuximab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. Drugs used in chemotherapy work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving cetuximab together with combination chemotherapy may kill more tumor cells.
PURPOSE: This phase II trial is studying how well giving cetuximab together with combination chemotherapy works as first-line therapy in treating patients with metastatic colorectal cancer.
OBJECTIVES:
Primary
Secondary
OUTLINE: This is a multicenter study.
Patients receive cetuximab IV over 1-2 hours on days 1 and 8. Patients also receive FOLFIRINOX chemotherapy comprising oxaliplatin IV over 2 hours, irinotecan hydrochloride IV over 30-90 minutes, and leucovorin calcium IV over 2 hours on day 1 and fluorouracil IV continuously over 46 hours on days 1 and 2. Treatment repeats every 15 days for up to 12 courses in the absence of disease progression or unacceptable toxicity.
After completion of study treatment, patients are followed every 3 months.
5,599 studies on the registry are indexed under Colorectal Neoplasms; 1,459 are open to participants now.
This study's enrollment of 42 is below the median of 77 across 4,123 interventional studies indexed under Colorectal Neoplasms.
Browse Colorectal Neoplasms studies →Institut du Cancer de Montpellier - Val d'Aurelle is the lead sponsor of 138 studies on the registry; 47 are open to participants now.
Counted across the registry records on this site, refreshed daily.
DISEASE CHARACTERISTICS:
Histologically confirmed colorectal cancer
Measurable disease, defined as ≥ 1 measurable lesion by MRI or CT scan
PATIENT CHARACTERISTICS:
PRIOR CONCURRENT THERAPY:
No prior chemotherapy for metastatic disease
5FU + Irinotecan + Oxaliplatine + Cetuximab
Biological: cetuximab · Drug: fluorouracil · Drug: irinotecan hydrochloride · Drug: leucovorin calcium · Drug: oxaliplatin
Complete response rate
Time frame: 6 months
Objective response rate
Time frame: 6 months
Adverse events by using NCI-CTC
Time frame: 6 months
Time to response
Time frame: 6 months
Time to progression
Time frame: 6 months
Survival
Time frame: 6 months
This study is completed, as verified in Feb 2026. You cannot join it, but the record below documents what was studied.
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Institut du Cancer de Montpellier - Val d'Aurelle