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NCT03493685Phase 3Completed

Study of Sparsentan in Patients With Primary Focal Segmental Glomerulosclerosis (FSGS)

Study Summary

To determine the long-term nephroprotective potential of treatment with sparsentan as compared to an angiotensin receptor blocker in patients with primary and genetic focal segmental glomerulosclerosis (FSGS).

Interventions / Drugs
View on ClinicalTrials.gov ↗
Study Details
Enrollment371 participants
Primary Completion2023-03-20
Lead SponsorTravere Therapeutics, Inc.
Data Retrieved2026-10-14
What This Trial Means for Biotech Investors
Trial Phase Context

Phase 3 trials are pivotal studies with large patient populations (hundreds to thousands) designed to prove efficacy and safety for FDA submission. A successful Phase 3 readout is typically the last major hurdle before a New Drug Application (NDA) or BLA filing.

Status & Expected Data

This trial has completed. Results may be available via ClinicalTrials.gov or peer-reviewed publications.

Primary completion: 2023-03-20
Enrolled: 371 participants
Sponsor Catalyst Profile

Travere Therapeutics (TVTX) is the sponsoring company for this trial. BiotechSign currently grades this company C (60/100) based on composite catalyst signals across its full pipeline. This trial is one data point in that overall catalyst picture.

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