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Study of Sparsentan Treatment in Pediatrics With Proteinuric Glomerular Diseases

Recruiting · Phase 2 · NCT05003986

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

At a glance

Research payments reported, 2025
$554,494
U.S. investigators named
18
Sites paid
17
Planned or actual enrollment
67

About the trial

Sponsor
Travere Therapeutics, Inc.
Tested
Sparsentan (drug), Sparsentan (drug), Sparsentan (drug)
Dates
Started 2021-08-12; completion 2027-04-12
Results posted
Not yet

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.

From ClinicalTrials.gov, last updated 2026-05-12. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Travere Therapeutics, Inc. reported $554,494 in research payments for this study in 2025 (165 payments).

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.