Study of Sparsentan Treatment in Pediatrics With Proteinuric Glomerular Diseases

Recruiting now · Phase 2

Conditions studied: Focal Segmental Glomerulosclerosis, Minimal Change Disease, Immunoglobulin A Nephropathy, IgA Vasculitis, Alport Syndrome

In brief

To evaluate the safety, efficacy and tolerability of sparsentan oral suspension and tablets, and assess changes in proteinuria after once-daily dosing over 108 weeks.

Key facts

Study ID
NCT05003986
Run by
Travere Therapeutics, Inc.
People needed
67
Starts
2021-08-12
Expected to finish
2027-04-12
Last updated by the study team
2026-05-12

Who can join

Age: 1 and older, up to 17. Sex: any. Healthy volunteers: not accepted.

Where it is running

Full record on ClinicalTrials.gov

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