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A Study of the Effect and Safety of Sparsentan in the Treatment of Patients With IgA Nephropathy
NCT03762850 · View on ClinicalTrials.gov ↗
Study Summary
To determine the long-term (approximately 2 years) nephroprotective potential of treatment with sparsentan as compared to an angiotensin receptor blocker in patients with immunoglobulin A nephropathy (IgAN).
Conditions Studied
Interventions
- DRUG Dapagliflozin
- DRUG sparsentan
- DRUG irbesartan
Study Locations (20)
California
- Travere Investigational Site — Glendale
- Travere Investigational Site — Montebello
- Travere Investigational Site — Northridge
- Travere Investigational Site — San Diego
- Travere Investigational Site — San Diego
- Travere Investigational Site — Stanford
Florida
- Travere Investigational Site — Coral Springs
- Travere Investigational Site — Hollywood
- Travere Investigational Site — Miami
- Travere Investigational Site — Miami
- Travere Investigational Site — Winter Park
Alabama
- Travere Investigational Site — Birmingham
- Travere Investigational Site — Homewood
Colorado
- Travere Investigational Site — Denver
Georgia
- Travere Investigational Site — Lawrenceville
Idaho
- Travere Investigational Site — Nampa
Illinois
- Travere Investigational Site — Hinsdale
Indiana
- Travere Investigational Site — Muncie
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 406 participants |
| Start Date | 2018-12-11 |
| Est. Completion | 2026-07 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03762850
The ClinicalTrials.gov registry entry for NCT03762850 describes a study currently listed as active not recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 406 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Travere Therapeutics, which has 9 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Immunoglobulin A Nephropathy appearing as the primary indexed condition, and to 3 interventions — of which Dapagliflozin is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT03762850 reports 20 study locations spanning 10 distinct geographic areas — top geographies include California, Florida, Alabama. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT03762850 about?
NCT03762850 is a clinical study titled "A Study of the Effect and Safety of Sparsentan in the Treatment of Patients With IgA Nephropathy". To determine the long-term (approximately 2 years) nephroprotective potential of treatment with sparsentan as compared to an angiotensin receptor blocker in patients with immunoglobulin A nephropathy (IgAN).
What is the current status of trial NCT03762850?
This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 406 participants. The study started on 2018-12-11. Estimated completion is 2026-07.
What conditions does trial NCT03762850 study?
This clinical trial studies the following conditions: Immunoglobulin A Nephropathy. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT03762850?
The interventions under investigation include: Dapagliflozin (DRUG), sparsentan (DRUG), irbesartan (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT03762850?
This trial is sponsored by Travere Therapeutics, which has 9 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT03762850 being conducted?
This trial has 20 study locations across Alabama, California, Colorado, Florida, Georgia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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