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Clinical trialNCT05856760CompletedPhase 2Interventional

A Study to Investigate Safety and Effect of Sparsentan in Combination With SGLT2 Inhibition in Participants With IgAN

SponsorTravere Therapeutics, Inc.Enrollment48Immunoglobulin A Nephropathy
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

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

Investigators

The overall officials registered on this study. Names that resolve to a FindMyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

30 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

Hong Kong
  • Travere Investigational Site

    Hong Kong, Hong Kong

  • Travere Investigational Site

    Kowloon, Hong Kong

  • Travere Investigational Site

    Shatin, Hong Kong

  • Travere Investigational Site

    Sheung Wan, Hong Kong

  • Travere Investigational Site

    Tsuen Wan, Hong Kong

United States
  • Travere Investigational Site

    Birmingham, Alabama, United States

  • Travere Investigational Site

    Chula Vista, California, United States

  • Travere Investigational Site

    Garden Grove, California, United States

  • Travere Investigational Site

    Glendale, California, United States

  • Travere Investigational Site

    Denver, Colorado, United States

  • Travere Investigational Site

    Boise, Idaho, United States

  • Travere Investigational Site

    Chubbuck, Idaho, United States

  • Travere Investigational Site

    Idaho Falls, Idaho, United States

  • Travere Investigational Site

    Chicago, Illinois, United States

  • Travere Investigational Site

    Evergreen Park, Illinois, United States

  • Travere Investigational Site

    Fort Wayne, Indiana, United States

  • Travere Investigational Site

    Kansas City, Kansas, United States

  • Travere Investigational Site

    Louisville, Kentucky, United States

  • Travere Investigational Site

    Shreveport, Louisiana, United States

  • Travere Investigational Site

    Albuquerque, New Mexico, United States

  • Travere Investigation Site

    Clifton Park, New York, United States

  • Travere Investigational Site

    Fresh Meadows, New York, United States

  • Travere Investigational Site

    New York, New York, United States

  • Travere Investigational Site

    Jacksonville, North Carolina, United States

  • Travere Investigational Site

    New Bern, North Carolina, United States

  • Travere Investigational Site

    Columbus, Ohio, United States

  • Travere Investigational Site

    Philadelphia, Pennsylvania, United States

  • Travere Investigational Site

    Columbia, South Carolina, United States

  • Travere Investigational Site

    Dallas, Texas, United States

  • Travere Investigational Site

    Dallas, Texas, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

Sparsentan
Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov ↗

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
19 May 2023
Primary completion
14 Oct 2024
Completion
25 Oct 2024
Last update posted
20 Nov 2025
Registered enrollment
48
Registry id
NCT05856760

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 4 Nov 2026. Registry facts are shown as registered by the study sponsor; FindMyKOL does not interpret them.