Your browser doesn't support javascript.
loading
Novel Treatment Paradigms: Primary IgA Nephropathy.
Selvaskandan, Haresh; Barratt, Jonathan; Cheung, Chee Kay.
Affiliation
  • Selvaskandan H; Mayer IgA Nephropathy Laboratories, Department of Cardiovascular Sciences, University of Leicester, Leicester, UK.
  • Barratt J; John Walls Renal Unit, University Hospitals of Leicester NHS Trust, Leicester, UK.
  • Cheung CK; Mayer IgA Nephropathy Laboratories, Department of Cardiovascular Sciences, University of Leicester, Leicester, UK.
Kidney Int Rep ; 9(2): 203-213, 2024 Feb.
Article in En | MEDLINE | ID: mdl-38344739
ABSTRACT
IgA nephropathy (IgAN) is the most common primary glomerulonephritis worldwide. Approximately 30% to 45% of patients progress to kidney failure (KF) within 20 to 25 years of diagnosis, and there has long been a lack of effective treatments. The therapeutic landscape in IgAN is rapidly evolving, driven in large part by the acceptance of the surrogate clinical trial end point of proteinuria reduction by regulatory authorities for the accelerated approval of new therapies. Two drugs, targeted release formulation (TRF)-budesonide (nefecon) and sparsentan, have recently been approved under this scheme. Advancing insights into the pathophysiology of IgAN, including the roles of the mucosal immune system, B-cells, the complement system, and the endothelin system have driven development of therapies that target these factors. This review outlines current, recently approved, and emerging therapies for IgAN.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Kidney Int Rep Year: 2024 Document type: Article Affiliation country: Reino Unido Country of publication: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Kidney Int Rep Year: 2024 Document type: Article Affiliation country: Reino Unido Country of publication: Estados Unidos