[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100584209":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":21,"centralContacts":26,"locations":20,"responsibleParty":32,"collaborators":20,"id":34,"slug":35,"hasResults":36,"nctId":37,"briefTitle":38,"officialTitle":39,"acronym":20,"eligibilityCriteria":40,"healthyVolunteers":36,"sex":41,"minAge":42,"maxAge":20,"enrollmentInfo":43,"targetDuration":20,"studyType":46,"phases":47,"briefSummary":49,"conditions":50,"keywords":20,"overallStatus":52,"whyStopped":20,"lastUpdateSubmitDate":53,"lastUpdatePostDateStruct":54,"startDateStruct":57,"completionDateStruct":59,"leadSponsor":61,"locationsCount":20},{"fullName":5,"class":6},"Dr. Falk Pharma GmbH","INDUSTRY",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"norucholic acid 1500 mg\u002Fday","EXPERIMENTAL","3 film-coated tablets once daily for 72 weeks containing in total norUrsodeoxycholic acid 1500 mg",[13],"Drug: norucholic acid",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":20},"DRUG","norucholic acid","500 mg norucholic acid film-coated tablets; 3 tablets\u002Fday",[9],null,[22],{"name":23,"affiliation":24,"role":25},"Michael Trauner, MD","Medical University of Vienna, dept. of Internal Medicine III","PRINCIPAL_INVESTIGATOR",[27],{"name":28,"role":29,"phone":30,"phoneExt":20,"email":31},"Michael Stiess, PhD","CONTACT","+497611514 Ext. 0","zentrale@drfalkpharma.de",{"type":33,"investigatorFullName":20,"investigatorTitle":20,"investigatorAffiliation":20,"oldNameTitle":20,"oldOrganization":20},"SPONSOR","100584209","phase-3-study-with-norucholic-acid-tablets-in-patients-with-primary-sclerosing-cholangitis-psc-100584209",false,"NCT06886360","Study with Norucholic Acid Tablets in Patients with Primary Sclerosing Cholangitis (PSC)","An Open-label Study of Patients with Primary Sclerosing Cholangitis (PSC) Treated with Norucholic Acid Tablets","Inclusion criteria:\n\n1. Signed informed consent.\n2. Males or females ≥ 18 years.\n3. Patient has previously been diagnosed with PSC, has participated in the previous NUC 5\u002FPSC trial and has completed the DBE phase with Visit 22, or has prematurely terminated the DBE phase before this trial has been started, or has prematurely terminated the DBE phase after this trial has been started, under the condition that the premature termination was due to lack of efficacy\\*. (\\*Lack of efficacy as defined in the NUC-5\u002FPSC trial.)\n\nExclusion Criteria:\n\n1. History or presence of chronic alcoholic consumption (daily consumption \\> 30 g in men, \\> 20 g in women).\n2. Patients who discontinued study participation in NUC-5\u002FPSC due to an AE possibly caused by the study drug.\n3. Liver Cirrhosis or any cirrhosis-related symptoms which in the opinion of the investigator may affect the patient's safety.\n4. History of liver transplantation or patient listed for transplantation.","ALL","18 Years",{"count":44,"type":45},120,"ESTIMATED","INTERVENTIONAL",[48],"PHASE3","Open-label, multi-center, phase III trial. Oral treatment with 1500 mg norucholic acid in Primary Sclerosing cholangitis",[51],"Primary Sclerosing Cholangitis","NOT_YET_RECRUITING","2025-03-19",{"date":55,"type":56},"2025-03-20","ACTUAL",{"date":58,"type":45},"2025-03",{"date":60,"type":45},"2027-09",{"name":5,"class":6}]