drugset / Trial / NCT07604311

Efficacy and Safety of Nefecon on Prevention of Relapse of IgA Nephropathy: a Randomized, Double-blinded, Placebo-Controlled Trial

NCT07604311 ↗

Phase 4 Not yet recruiting 288 enrolled Nanfang Hospital, Southern Medical University
RandomizedParallel-groupQuadruple-blindTreatment

Summary

IgA nephropathy (IgAN) is a chronic progressive kidney disease, and long-term control of proteinuria and prevention of relapse are crucial for delaying disease progression. Patients with IgAN who achieve proteinuria remission after receiving Nefecon for 9 months or longer still face the risk of proteinuria relapse after treatment discontinuation. This study is to evaluate the efficacy and safety of Nefecon 8 mg treatment for 15 months as a maintenance therapy for prevention of proteinuria relapse in proteinuria-remitted patients.

Timeline

Start
2026-05-01
Primary completion
2028-12-01
Completion
2028-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Nefecon Unknown 8 mg Oral