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Study of Sparsentan Treatment in Pediatrics With Proteinuric Glomerular Diseases

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NCT05003986 · readout in 205 d

Sponsored by Travere Therapeutics, Inc. (industry) · TVTX — their whole pipeline →.

Phase
Phase 2
Status
Recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
67estimated
Sites
47
Countries
Germany, Italy, Netherlands +5

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2021-08-12actualWhen the study began enrolling
Primary completion2027-03-12estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2027-04-12estimatedThe whole study's end, after follow-up
First posted2021-08-13actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-05-12actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Focal Segmental Glomerulosclerosis
  • Minimal Change Disease
  • Immunoglobulin A Nephropathy
  • IgA Vasculitis
  • Alport Syndrome

Interventions

  • Drug: Sparsentan — also filed as RE-021
  • Drug: Sparsentan — also filed as RE-021
  • Drug: Sparsentan — also filed as RE-021

Primary outcomes

what the primary-completion date above is the date OF
Incidence of treatment-emergent adverse events (TEAEs), serious adverse events (SAEs), AEs leading to treatment discontinuation, and adverse events of interest (AEOIs)
measured After the last patient has undergone the week 108 visit (Visit 15).
Urine protein/creatinine ratio (UP/C) at week 108
measured After the last patient has undergone the Week 108 visit (Visit 15)

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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