RecruitingPhase 2NCT04663204

A Study of the Safety and Activity of Sparsentan for the Treatment of Patients With Immunoglobulin A Nephropathy

A Multi-centre, Open-label, Exploratory Trial of the Safety and Activity of Sparsentan for the Treatment of Incident (Cohort A) and Recurrent (Cohort B) Patients With Immunoglobulin A Nephropathy


Sponsor

University of Leicester

Enrollment

24 participants

Start Date

Dec 10, 2020

Study Type

INTERVENTIONAL

Conditions

Summary

To determine the nephroprotective potential of treatment with sparsentan in (1: Cohort A) patients newly-diagnosed with immunoglobulin A nephropathy (IgAN) (ie, incident patients) who have not received prior angiotensin-converting enzyme inhibitor (ACEI) or angiotensin receptor blocker (ARB) therapy, and in (2: Cohort B) patients with recurrent IgAN following kidney transplantation.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Sparsentan for people with autoimmune diseases, glomerulonephritis, and other related conditions. The study is currently recruiting participants at 6 locations. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGSparsentan

Target dose of 400 mg daily


Locations(6)

Cambridge University Hospitals NHS Trust

Cambridge, England, United Kingdom

Northern Care Alliance NHS Foundation Trust - Salford Royal

Salford, England, United Kingdom

Royal Infirmary of Edinburgh & Western General Hospital

Edinburgh, Scotland, United Kingdom

University Hospital of wales

Cardiff, Wales, United Kingdom

Leicester General Hospital, University Hospitals of Leicester NHS Trust

Leicester, United Kingdom

King's College Hospital

London, United Kingdom

View Full Details on ClinicalTrials.gov

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NCT04663204


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