
Animation – Long-Term Outcomes in IgA Nephropathy : Results From RaDaR
Understand the relationship between proteinuria and IgA nephropathy outcomes based on findings from the RaDaR registry for rare kidney diseases.
Travere Therapeutics
The UK National Registry of Rare Kidney Diseases (RaDaR) collects clinical data from patients with rare kidney diseases, such as IgA nephropathy.
Over 2,400 patients were included in the IgA nephropathy cohort of RaDaR.
Based on the 2021 Kidney Disease Improving Global Outcomes (KDIGO) 2021 Clinical Practice Guideline for the Management of Glomerular Diseases, healthcare professionals have previously grouped patients as “low risk” or “high risk”
But more information on long-term outcome on low-risk IgA nephropathy was needed.
The following were measured:
Outcomes in this large cohort of patients with IgA nephropathy were generally poor, including in patients traditionally considered “low risk” (<1 g/day)
In general, reducing proteinuria was associated with better outcomes in patients with IgA nephropathy.
IgA nephropathy is the most common type of primary glomerulonephritis and leading cause of chronic kidney disease (CKD) and kidney failure.
To work toward the goal of preventing kidney failure in IgA nephropathy, the current approach to patient care needs to be re-evaluated to improve clinical outcomes.
Findings from the RaDaR study demonstrated a growing need to:
Using data in part from the RaDaR study, the 2025 KDIGO Clinical Practice Guideline for the Management of IgA Nephropathy and IgA Vasculitis (IgAV) have redefined risk of progressive loss of kidney function as ≥0.5 g/d.
MA-DS-24-0041 | October 2025
Understand the relationship between proteinuria and IgA nephropathy outcomes based on findings from the RaDaR registry for rare kidney diseases.
Understand the relationship between proteinuria and IgA nephropathy outcomes based on findings from the RaDaR registry for rare kidney diseases.

