[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"heterogenic\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:heterogenic":31},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":4,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":33,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":46,"locationsCount":5},"100565889","research-of-therapeutic-targets-in-the-frame-of-nephronophthisis-and-renal-associated-ciliopathies-100565889",false,"NCT06648044","Research of Therapeutic Targets in the Frame of Nephronophthisis and Renal Associated Ciliopathies","Research of Therapeutic Targets in the Frame of Nephronophthisis and Renal Associated Ciliopathies - NPH_1","NPH1","Inclusion Criteria:\n\n* In order to be included in the protocol, subjects will have to respect the following criteria:\n\nAffected patients:\n\nSuffering from nephronophthisis or renal associated ciliopathies with known genetic diagnosis or not, Having obtained the signature of the informed consent form of patient, parent(s) or legal representative No age limit is requested for these patients, who can be recruited from birth.\n\nHealthy relatives:\n\nBeing the healthy relative (father \u002F mother \u002F brother \u002F sister) of an included patient Having signed the informed consent form (patient or parent in case of minor subject) No age limit is requested for these subjects, who can be recruited from birth.\n\n'Negative' control patients: Being unscathed of any chronic renal disease, with or without ciliopathies Having obtained the signature of the informed consent form No age limit is requested for these patients, who can be recruited from birth.\n\n'Positive' control patients Suffering from Chronic Kidney Disease unrelated to ciliary dysfunction (such as glomerulopathy, tubulopathy…) Having obtained the signature of the informed consent form No age limit is requested for these patients, who can be recruited from birth.\n\nExclusion Criteria:\n\nIn order to be included in the protocol, subjects will have to fulfill none of the following criteria:\n\nAffected patients:\n\nPatients with a functioning kidney transplant (only for patient for who urine sample is performed. This criteria is not applicable when only blood is sampling) Patients included in a therapeutic protocol since fewer 30 days.\n\nHealthy relatives:\n\nNo no-inclusion criteria\n\n'Negative' control subjects: No no-inclusion criteria\n\n'Positive' control subjects: Patients with a functioning kidney transplant",true,"ALL",{"count":20,"type":21},310,"ESTIMATED","INTERVENTIONAL",[24],"NA","Nephronophthisis (NPH) is an autosomal recessive, genetically heterogeneous disease, with mutations identified in over 20 genes (notably NPHP1 and NPHP4).\n\nThese genetic defects are associated with reduced urine concentration, chronic tubulointerstitial nephritis, etc., and progress to end-stage renal failure before the age of 20.\n\nNephronophthisis may occur as an isolated pathology, but is also often associated with various extrarenal symptoms.\n\nNPHP genes account for around 50% of the genes responsible for NPH. No effective treatment is available to date.\n\nStudying NPHP proteins and associated signaling pathways could help identify how to circumvent the problems of protein distribution and therapeutic mRNA, and could be applicable to a broad set of NPHP mutations. To this end, Dr. Saunier's laboratory at Institut Imagine has recently identified approved drugs that correct some of the ciliary and epithelial defects found in cells with NPHP mutations.",[27,15,28,29,30,31,32],"Nephronophthisis","Autosomal","Recessive","Genetically","Heterogenic","Disorder",[34,35,36],"mutations","20","genes","RECRUITING","2025-08-29",{"date":40,"type":41},"2025-09-05","ACTUAL",{"date":43,"type":41},"2016-02-01",{"date":45,"type":21},"2028-02-01",{"name":47,"class":48},"Imagine Institute","OTHER"]