NCT02980510CompletedPhase 2
Comparison FOLFIRINOX Panitumumab vs mFOLFOX6 Panitumumab in RAS/B-RAF Wild-type Metastatic Colorectal Cancer Patients
Phase II Randomized Study Comparing FOLFIRINOX + Panitumumab Versus mFOLFOX6 + Panitumumab in Metastatic Colorectal Cancer Patients Selected by RAS and B-RAF Status From Circulating DNA Analysis
Source: ClinicalTrials.gov · Last updated 29 Sept 2026
Brief summary (registry, in English)
National trial, multicenter, randomized, phase II assessing FOLFIRINOX + Panitumumab versus mFOLFOX6 + Panitumumab in metastatic colorectal cancer patients selected by RAS and B-RAF status from circulating DNA analysis. Evaluation of complete response rate on treatment combining FOLFIRINOX and panitumumab.
- Status (registry)
- Completed
- Phase (registry)
- Phase 2
- Study type
- Interventional
- Enrollment
- 219 (actual)
- First submitted
- 30 Nov 2016
- Start date
- Dec 2016
- Primary completion date
- Dec 2025
- Lead sponsor
- UNICANCER
- Diseases
- Colorectal cancer
- NCT number
- NCT02980510
- EU CT number
- 2024-510645-34-00
- EudraCT number
- 2016-001490-33
What you commit to
- Study type: Interventional · Phase 2
- Participants enrolled: 219
- From Dec 2016 to the primary completion date, Dec 2025
- 23 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study design.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Adjuvant treatment with oxaliplatin
- Previous treatment for metastatic disease
- Patients who received any chemo- and/or radiotherapy within 15 days from the date of blood sampling for the RAS and BRAF test
- Previous organ transplantation, HIV or other immunodeficiency syndromes
- Concomitant medications/comorbidities that may prevent the patient from receiving study treatment as uncontrolled intercurrent illness (for instance: active infection, active inflammatory disorders, inflammatory bowel disease, intestinal obstruction, symptomatic congestive heart failure, uncontrolled hypertension…)
- Patient with contraindication for trial drugs (investigators have to refer to SmPC drugs, see Appendix 7)
- Concomitant intake of St. John's wort
- Other concomitant cancer
Other illness
- History of other malignancy within the previous 5 years (except for appropriately treated in-situ cervix carcinoma and non-melanoma skin carcinoma)
- Patients with a history of severe or life-threatening hypersensitivity to the active substances or to any of the excipients delivered in this study
- Patient with history of pulmonary fibrosis or interstitial pneumonitis
- Ionic disorders as:
- Kalemia ≤1 x LLN
- Magnesemia \<0.5mmol/L
- Calcemia \<2mmol/L
- Patients with psychological, familial, sociological or geographical condition hampering compliance with the study protocol and follow-up schedule
Lab values
- QT/QTc\>450msec for men and \>470msec for women
Other
- Brain metastases
- Persistent peripheral neuropathy \>grade1 (NCI CT v4.03)
- Patient with known dihydropyrimidine dehydrogenase deficiency
- Participation in another therapeutic trial
- Pregnant woman or lactating woman
- Legal incapacity or limited legal capacity
Who the study is looking for
- Age between 18 and 75 years
- ECOG PS between 0 and 1
- Histologically confirmed adenocarcinoma of the colon or rectum
- Untreated synchronous or metachronous metastatic disease deemed unresectable with curative intent
- K-Ras (codons 12, 13, 59, 61, 117, 146), N-Ras (codons 12, 13, 59, 61) and B-Raf (codon 600) wild-type tumor status according to plasma analysis of circulating cell free DNA by Intplex technology
- Measurable disease according to RECIST version 1.1
- Adequate hematologic, hepatic and renal functions:
- Absolute neutrophil count (ANC) ≥2 x 109/L
- Haemoglobin ≥9 g/dL
- Platelets (PTL) ≥100 x 109/L
- AST/ALT ≤5 x ULN
- Alkaline phosphatase ≤2.5 x ULN
- Bilirubin ≤1.5 x ULN
- Creatinine clearance ≥50 mL/min (Cockcroft and Gault formula)
- Life expectancy of at least 3 months
- Adequate contraception if applicable
- Patient affiliated to a social security regimen
- Patient information and signed written consent form
- Uracilemia \< 16 ng/ml
Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers
Sites (23)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Institut de Cancerologie de L'Ouest Coordinator of this site? Confirm its status | Angers | France | Active, not recruiting |
| Institut Bergonie Coordinator of this site? Confirm its status | Bordeaux | France | Active, not recruiting |
| Centre Francois Baclesse Coordinator of this site? Confirm its status | Caen Cedex 5 | France | Active, not recruiting |
| Centr Georges Francois Leclerc Coordinator of this site? Confirm its status | Dijon | France | Active, not recruiting |
| Groupement Des Hopitaux De L'Institut Catholique De Lille Coordinator of this site? Confirm its status | Lille Cedex | France | Active, not recruiting |
| Hôpital Privé Jean Mermoz Coordinator of this site? Confirm its status | Lyon | France | Active, not recruiting |
| Centre Leon Berard Coordinator of this site? Confirm its status | Lyon | France | Active, not recruiting |
| Hopital Europeen Marseille Coordinator of this site? Confirm its status | Marseille | France | Active, not recruiting |
| Centre De Cancerologue Du Grand Montpellier Coordinator of this site? Confirm its status | Montpellier | France | Active, not recruiting |
| Centre Hospitalier Universitaire De Montpellier Coordinator of this site? Confirm its status | Montpellier Cedex 5 | France | Active, not recruiting |
| Institut Regional Du Cancer De Montpellier Coordinator of this site? Confirm its status | Montpellier Cedex 5 | France | Active, not recruiting |
| L'Hopital Prive Du Confluent Coordinator of this site? Confirm its status | Nantes Cedex 2 | France | Active, not recruiting |
| Centre Antoine Lacassagne Coordinator of this site? Confirm its status | Nice Cedex 2 | France | Active, not recruiting |
| Assistance Publique Hopitaux de Paris Coordinator of this site? Confirm its status | Paris | France | Active, not recruiting |
| Centre Catalan d'Oncologie Coordinator of this site? Confirm its status | Perpignan | France | Active, not recruiting |
| Centre Hospitalier De Perpignan Coordinator of this site? Confirm its status | Perpignan Cedex | France | Active, not recruiting |
| Centre Hospitalier Universitaire de Bordeaux Coordinator of this site? Confirm its status | Pessac | France | Active, not recruiting |
| Hôpital Privé des Côtes d'Armor Coordinator of this site? Confirm its status | Plérin | France | Active, not recruiting |
| Institut Godinot Coordinator of this site? Confirm its status | Reims | France | Active, not recruiting |
| Centre Hospitalier Universitaire Reims Coordinator of this site? Confirm its status | Reims Cedex | France | Active, not recruiting |
| CHU De Rouen Coordinator of this site? Confirm its status | Rouen Cedex | France | Active, not recruiting |
| Institut De Cancerologie De L Ouest Coordinator of this site? Confirm its status | St Herblain | France | Active, not recruiting |
| Institut de cancérologie de Lorraine Coordinator of this site? Confirm its status | Vandoeuvre Les Nancy_ Cedex | France | Active, not recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.