A Study to Investigate Safety and Effect of Sparsentan in Combination With SGLT2 Inhibition in Participants With IgAN
Part of paid clinical trials in Birmingham, Alabama.
- Sponsor
- Travere Therapeutics, Inc.
- Study ID
- NCT05856760
- Phase
- PHASE2
- Status
- Completed
Conditions
- Immunoglobulin A Nephropathy
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Sparsentan — DRUGTarget dose of 400 mg daily
Study Details
This was a 28-week, open-label, multicenter, single-group Phase 2 exploratory study to determine the safety and effect of sparsentan in participants with IgAN who are at risk of disease progression to kidney failure despite being on both stable RAASi and SGLT2 inhibitor treatment for at least 12 weeks prior to study entry
Key Dates
- Start date
- May 19, 2023
- Status verified
- Sep 2025
- Primary completion
- Oct 14, 2024
- Completion
- Oct 25, 2024
Study Design
- Enrollment
- 48 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: sparsentanSparsentan will be administered daily as a 200-mg oral tablet. The goal is to titrate from the initial dose of 200 mg (Day 1) to the target dose of 400 mg at Week 2.
Primary Outcome Measure
Change in Urine Albumin-creatinine Ratio (UA/C) at Week 24 [ Time Frame: Week 24 ]
Locations (25)
Related coverage on Hipa.ai
- Sparsentan Phase 2 Study in IgAN Shows Significant UA/C ReductionSparsentan · Nov 20, 2025 · ClinicalTrials.gov
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