HomeTrialNCT05003986
NCT05003986Phase 2RECRUITING

Study of Sparsentan Treatment in Pediatrics With Proteinuric Glomerular Diseases

Study Summary

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.

Interventions / Drugs
View on ClinicalTrials.gov ↗
Study Details
Enrollment67 participants
Primary Completion
Lead SponsorTravere Therapeutics, Inc.
Data Retrieved2026-04-11 04:30:13.943001+00:00
What This Trial Means for Biotech Investors
Trial Phase Context

Phase 2 trials begin testing efficacy in a larger patient group (100–300). This is often where biotech binary events occur — positive Phase 2 data can significantly advance a company's pipeline narrative, while failures can be terminal for a program.

Status & Expected Data

Currently recruiting: the trial is enrolling patients. A data readout is not expected until after enrollment closes and the follow-up period is complete.

Enrolled: 67 participants
Sponsor Catalyst Profile

Travere Therapeutics (TVTX) is the sponsoring company for this trial. BiotechSign currently grades this company C (61/100) based on composite catalyst signals across its full pipeline. This trial is one data point in that overall catalyst picture.

Not financial advice. BiotechSign data is sourced from ClinicalTrials.gov, SEC EDGAR, and other public databases for research and informational purposes only. It does not constitute investment recommendations. Always do your own due diligence before making investment decisions.