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NCT07219121 · ClinicalTrials.gov registry record · Phase 4

Sparsentan in Posttransplant Immunoglobulin A Nephropathy or Focal Segmental Glomerulosclerosis

A Phase 4 study of Kidney Transplant and Focal Segmental Glomerulosclerosis, sponsored by Travere Therapeutics.

Recruiting
Registry status
Phase 4
Development phase
20
Enrollment target
9
Study locations

NCT07219121 is a Phase 4 study of Kidney Transplant and Focal Segmental Glomerulosclerosis that is actively recruiting participants, run by Travere Therapeutics. The registered enrollment target is 20 participants, below the 1,898-participant average among 30 other Kidney Transplant trials with a reported enrollment target (99% lower). The trial reports 9 study locations across 8 states.

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The verdict

NCT07219121, a Phase 4 study of Kidney Transplant and Focal Segmental Glomerulosclerosis, is actively recruiting participants, sponsored by Travere Therapeutics.

RECRUITING
Registry status
Phase 4
Development phase
20 participants
Enrollment target
9
Study locations

Study Summary

To evaluate the safety and efficacy of sparsentan tablets for the treatment of patients with proteinuria after kidney transplantation with once-daily dosing for 36 weeks.

Interventions

  • DRUG Sparsentan

Study Locations (9)

Texas

  • Dallas Nephrology Associates - Dallas
  • University of Texas - Galveston

Alabama

  • University of Alabama at Birmingham - Birmingham

New York

  • Cornell Medical Center - New York

North Carolina

  • University of North Carolina Chapel Hill - Morrisville

Ohio

  • Ohio State University - Columbus

Pennsylvania

  • University of Pittsburgh Medical Center - Pittsburgh

Washington

  • University of Washington - Seattle

Wisconsin

  • University of Wisconsin - Madison

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2025-10-07
Est. Completion 2027-05
Phase Phase 4

Sponsor

Travere Therapeutics

12 total trials

What the Registry Record Tells You About NCT07219121

The ClinicalTrials.gov registry entry for NCT07219121 describes a study currently listed as recruiting, categorized as Phase 4. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,898-participant average among 30 other Kidney Transplant trials with a reported enrollment target (99% lower). The listed sponsor is Travere Therapeutics, which has 12 total studies on file at ClinicalTrials.gov.

The record links to 4 conditions, with Kidney Transplant appearing as the primary indexed condition, and to 1 intervention - of which Sparsentan is the first listed.

NCT07219121 reports 9 study locations spanning 8 distinct geographic areas - top geographies include Texas, Alabama, New York.

Frequently Asked Questions

What is clinical trial NCT07219121 about?

NCT07219121 is a clinical study titled "Sparsentan in Posttransplant Immunoglobulin A Nephropathy or Focal Segmental Glomerulosclerosis". To evaluate the safety and efficacy of sparsentan tablets for the treatment of patients with proteinuria after kidney transplantation with once-daily dosing for 36 weeks.

What is the current status of trial NCT07219121?

This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 20 participants. The study started on 2025-10-07. Estimated completion is 2027-05.

What conditions does trial NCT07219121 study?

This clinical trial studies the following conditions: Kidney Transplant, Focal Segmental Glomerulosclerosis, Proteinuria, Immunoglobulin A (IgA) Nephropathy.

What interventions are being tested in trial NCT07219121?

The interventions under investigation include: Sparsentan (DRUG).

Who is sponsoring clinical trial NCT07219121?

This trial is sponsored by Travere Therapeutics, which has 12 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07219121 being conducted?

This trial has 9 study locations across Alabama, New York, North Carolina, Ohio, Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.