[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100515231":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":19,"centralContacts":20,"locations":31,"responsibleParty":52,"collaborators":19,"id":54,"slug":55,"hasResults":56,"nctId":57,"briefTitle":58,"officialTitle":59,"acronym":60,"eligibilityCriteria":61,"healthyVolunteers":56,"sex":62,"minAge":63,"maxAge":19,"enrollmentInfo":64,"targetDuration":19,"studyType":67,"phases":68,"briefSummary":70,"conditions":71,"keywords":73,"overallStatus":34,"whyStopped":19,"lastUpdateSubmitDate":76,"lastUpdatePostDateStruct":77,"startDateStruct":80,"completionDateStruct":82,"leadSponsor":84,"locationsCount":85},{"fullName":5,"class":6},"Centre Georges Francois Leclerc","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"FOLFIRINOX treatment","EXPERIMENTAL","Treatment with FOLFIRINOX3 will be administered with a maximum of 16 courses divided into two 8-course doses.\n\nMaintenance treatment (folinic acid\u002Fcalcium levofolinate + 5-FU) will be administered until progression.",[13],"Drug: FOLFIRINOX treatment",[15],{"type":16,"name":9,"description":17,"armGroupLabels":18,"otherNames":19},"DRUG","Treatment with FOLFIRINOX3 will be administered with a maximum of 16 courses divided into two 8-course doses.\n\nMaintenance treatment (folinic acid\u002Fcalcium levofolinate + 5-FU) will be administered until progression",[9],null,[21,27],{"name":22,"role":23,"phone":24,"phoneExt":25,"email":26},"Jean-David FUMET, Dr","CONTACT","380737538","+33","jdfumet@cgfl.fr",{"name":28,"role":23,"phone":29,"phoneExt":25,"email":30},"Sophie PARNALLAND, Project manager","345348077","sparnalland@cgfl.fr",[32],{"facility":33,"status":34,"city":35,"state":19,"zip":36,"country":37,"countryCode":38,"cosmosGeoPoint":39,"geoPoint":44,"contacts":45},"Centre Georges-François Leclerc","RECRUITING","Dijon","21000","France","FR",{"type":40,"coordinates":41},"Point",[42,43],5.01391,47.31344,{"lat":43,"lon":42},[46,49],{"name":47,"role":23,"phone":48,"phoneExt":25,"email":26},"Fumet Jean David, Dr","03 80 73 75 00",{"name":50,"role":23,"phone":51,"phoneExt":25,"email":30},"Sophie Parnalland","03 45 34 80 77",{"type":53,"investigatorFullName":19,"investigatorTitle":19,"investigatorAffiliation":19,"oldNameTitle":19,"oldOrganization":19},"SPONSOR","100515231","phase-2-trial-evaluating-the-efficacy-and-the-safety-of-folfirinox3-treatment-in-patients-with-unresectable-locally-advanced-or-metastatic-pancreatic-cancer-in-first-line-of-chemotherapy-100515231",false,"NCT05988814","Trial Evaluating the Efficacy and the Safety of FOLFIRINOX3 Treatment in Patients With Unresectable Locally Advanced or Metastatic Pancreatic Cancer in First Line of Chemotherapy","Phase II Trial Evaluating the Efficacy and the Safety of FOLFIRINOX3 Treatment in Patients With Unresectable Locally Advanced or Metastatic Pancreatic Cancer in First Line of Chemotherapy (FOLFIRINOX3 Pancréas)","FOLFIRINOX3 P","Inclusion Criteria:\n\n* Male or female age \\> 18 years at time of study entry\n* Performance status of 0 or 1 according to the Eastern Cooperative Oncology Group (ECOG)\n* Patients with pancreatic adenocarcinoma\n* Patients with unresectable locally advanced pancreatic cancer or metastatic pancreatic cancer\n* Patients with no history of chemotherapy (prior adjuvant or neoadjuvant chemotherapy accepted if the time between the end of chemotherapy and recurrence is greater than 12 months) and no history of curative radiotherapy for metastatic or locally advanced disease. Palliative radiotherapy is accepted.\n* Patient eligible for treatment with FOLFIRINOX (5-FU, Irinotecan, Oxaliplatin and folinic acid) including but not limited to: No active heart disease An ECG with a QT\u002FQTc interval ˂ to 450 ms for men and ˂ to 470 ms for women. No uncontrolled hypertension defined by systolic pressure \\> 140 mmHg or diastolic pressure \\> 90 mmHg despite optimal medical management. A negative pregnancy test if applicable\n* Tumor evaluation (CT scan) performed within 4 weeks (28 days) prior to inclusion with at least one measurable lesion according to RECIST 1.1 criteria\n* Patient fit and able to comply with the protocol for the duration of the study, including treatment, visits, scheduled examinations and follow-up.\n* Biological, hepatic, renal and serological data within the following limits (tests performed within 7 days of inclusion except for serologies performed within 28 days)\n* Information given and informed consent signed\n* Patient affiliated to a social security scheme\n* Men and women must have an effective contraceptive method.\n\nExclusion Criteria:\n\n* Patient with neuroendocrine carcinoma or acinar cell carcinoma\n* Other cancer in the 5 years preceding inclusion or concomitant (except cancer in situ of the uterine cervix or cutaneous basal cell carcinoma).\n* Presence of brain metastasis(es)\n* Estimated prognosis \\\u003C 3 months\n* History of grade 4 toxicity to oxaliplatin, irinotecan or 5FU if history of adjuvant\u002Fneoadjuvant chemotherapy\n* Sequellar toxicity \\> grade 1 if previous adjuvant\u002Fneoadjuvant chemotherapy\n* Hypersensitivity to any component of FOLFIRINOX® treatment.\n* Current participation or participation within 30 days prior to inclusion in another therapeutic trial with an investigational compound and\u002For completion of radiotherapy within 10 days prior to the start of treatment\n* Evidence of a homozygous or heterozygous DPYD mutation and\u002For uracilemia \\>16ng\u002FmL and\u002For homozygous UGT1A1 genotype.\n* Pregnancy, breastfeeding\n* Inability to sign informed consent or to undergo medical monitoring of the trial for geographical, social or psychological reasons including, but not limited to, psychiatric illness compromising comprehension of information or conduct of the study.\n* Patient under guardianship, curatorship or safeguard of justice.","ALL","18 Years",{"count":65,"type":66},90,"ESTIMATED","INTERVENTIONAL",[69],"PHASE2","Evaluate the efficacy of treatment FOLFORINOX 3 in first-line therapy for patients with locally advanced unresectable or metastatic pancreatic cancer.",[72],"Metastatic Pancreatic Cancer",[9,74,75],"pancreatic cancer","first line chemotherapy","2024-02-09",{"date":78,"type":79},"2024-02-12","ACTUAL",{"date":81,"type":79},"2024-01-24",{"date":83,"type":66},"2029-07-24",{"name":5,"class":6},1]