[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100560679":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":11,"centralContacts":27,"locations":11,"responsibleParty":33,"collaborators":11,"id":37,"slug":38,"hasResults":39,"nctId":40,"briefTitle":41,"officialTitle":42,"acronym":43,"eligibilityCriteria":44,"healthyVolunteers":39,"sex":45,"minAge":46,"maxAge":11,"enrollmentInfo":47,"targetDuration":11,"studyType":50,"phases":51,"briefSummary":53,"conditions":54,"keywords":11,"overallStatus":56,"whyStopped":11,"lastUpdateSubmitDate":57,"lastUpdatePostDateStruct":58,"startDateStruct":61,"completionDateStruct":63,"leadSponsor":65,"locationsCount":11},{"fullName":5,"class":6},"Zhejiang University","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Finerenone","EXPERIMENTAL",null,[13],"Drug: Finerenone",{"label":15,"type":16,"description":11,"interventionNames":17},"placebo","PLACEBO_COMPARATOR",[18],"Drug: Placebo",[20,24],{"type":21,"name":9,"description":22,"armGroupLabels":23,"otherNames":11},"DRUG","10mg or 20mg",[9],{"type":21,"name":25,"description":22,"armGroupLabels":26,"otherNames":11},"Placebo",[15],[28],{"name":29,"role":30,"phone":31,"phoneExt":11,"email":32},"Guizhen Yu","CONTACT","15268801632","gzysmile@126.com",{"type":34,"investigatorFullName":35,"investigatorTitle":36,"investigatorAffiliation":5,"oldNameTitle":11,"oldOrganization":11},"PRINCIPAL_INVESTIGATOR","Du Xiaoying","chief physician","100560679","phase-3-effect-of-finerenone-in-iga-nephropathy-100560679",false,"NCT06580288","Effect of Finerenone in IgA Nephropathy","A Multicenter, Randomized, Double-blind, Placebo-controlled Clinical Trial of Finerenone in the Treatment of IgA Nephropathy","FIGHT","Inclusion Criteria:\n\n* Kidney biopsy confirmed IgA nephropathy within 2 years, with secondary IgA nephropathy excluded;\n* Age ≥ 18 years;\n* Maximum tolerated dose of RAS inhibitors for more than 3 months, with urine albumin\u002Fcreatinine ratio ≥ 500 mg\u002Fg and ≤ 3500 mg\u002Fg; V1 laboratory test showing urine albumin\u002Fcreatinine ratio ≥ 500 mg\u002Fg and ≤ 3500 mg\u002Fg. After maximum tolerated dose of RAS inhibitors or ARB, V2 urine albumin\u002Fcreatinine ratio ≥ 500 mg\u002Fg and ≤ 3500 mg\u002Fg;\n* eGFR calculated by EPI ≥ 30 ml\u002Fmin\u002F1.73 m²;\n* Serum potassium level ≤ 4.8 mmol\u002FL;\n* SBP ≤ 150 mmHg, DBP ≤ 110 mmHg;\n* LVEF \\> 40%;\n* Willing and able to provide informed consent.\n\nExclusion Criteria:\n\n* There are clear indications for the use of immunosuppressive therapy, such as: nephrotic syndrome (urine protein greater than 3.5 g\u002Fd, blood albumin less than 30 g\u002FL), pathological minimal change disease combined with IgA nephropathy; the proportion of crescents in kidney biopsy is ≥ 50%.\n* Any existing life-threatening condition with a life expectancy of less than 2 years;\n* Active infection, HBV infection, or active lesions (nodules, cavities, or tuberculomas);\n* AKI causing renal dysfunction;\n* Use of steroids\u002Fimmunosuppressive drugs within the past 3 months;\n* History of malignant tumors, regardless of treatment status or evidence of local recurrence or metastasis;\n* Any surgical or medical condition that may significantly alter the absorption, distribution, metabolism, or excretion of the investigational drug;\n* History of drug or alcohol abuse within the past 12 months;\n* History of drug allergies or contraindications;\n* Previous noncompliance or unwillingness to follow the study protocol;\n* Any condition that may affect safety or efficacy;\n* History of kidney transplantation or currently receiving immunosuppressive treatment;\n* Pregnant or breastfeeding women;\n* Obese patients with a BMI \\> 35.","ALL","18 Years",{"count":48,"type":49},120,"ESTIMATED","INTERVENTIONAL",[52],"PHASE3","The aim of this trial is to conduct a randomized, multicenter, placebo-controlled, double-blind clinical trial to determine the safety and efficacy of Finerenone in reducing proteinuria and protecting renal function in patients with IgA nephropathy.\n\nThe primary endpoint event was the change in urinary albumin\u002Fcreatinine ratio between the two groups at 12 months of treatment.",[55],"IgA Nephropathy","NOT_YET_RECRUITING","2024-08-28",{"date":59,"type":60},"2024-08-30","ACTUAL",{"date":62,"type":49},"2024-10-08",{"date":64,"type":49},"2026-10-08",{"name":5,"class":6}]