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NCT07315191: FICHSPN

Finerenone Therapy for Pediatric HSPN With Mild Proteinuria

Recruiting now Phase 4 Last updated 7 January 2026
What this trial tests

Phase 4 trial testing ACEI / ARB+finerenone in Henoch Schönlein Purpura Nephritis in 116 participants. Currently enrolling.

Timeline
13 June 2025
Primary endpoint
31 October 2027
30 April 2028

Quick facts

Lead sponsorCapital Institute of Pediatrics, China
PhasePhase 4
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment116
Start date13 June 2025
Primary completion31 October 2027
Estimated completion30 April 2028
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Capital Institute of Pediatrics, China

Who can join

Adults 3 to 18, any sex, with Henoch Schönlein Purpura Nephritis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Henoch-Schönlein purpura nephritis (HSPN) is the most common secondary glomerular disease in children. About 40% of HSPN cases are accompanied by mild proteinuria, and some of them progress to end-stage renal disease. Currently, the treatment for children with mild proteinuria HSPN mainly involves ACEI/ARB, but long-term use of these drugs can lead to an increase in aldosterone levels, affecting therapeutic efficacy. Finerenone can improve vascular endothelial cell dysfunction and renal tissue inflammation and fibrosis, and reduce urinary protein in patients with glomerular diseases. This study intends to conduct an exploratory randomized controlled clinical trial of finerenone in children with HSPN accompanied by a small amount of proteinuria to evaluate the efficacy and safety of finerenone treatment.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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