Kerendia (finerenone) - Bayer
lorundrostat (MT-4129) - Mineralys Therapeutics
vicadrostat (BI 690517) - Boehringer Ingelheim
ziltivekimab (COR-001) - Novo Nordisk
avenciguat (BI 685509) - Boehringer Ingelheim
Baxfendy (baxdrostat) - AstraZeneca
Pharmacokinetics of novel drugs for the treatment of Diabetic nephropathy. (PubMed, Expert Opin Drug Metab Toxicol) - Sep 9, 2026 - "Evidence was synthesized for sodium-glucose cotransporter-2 inhibitors (SGLT2i), glucagon-like peptide-1 receptor agonists (GLP-1RA), dual incretin agonists, nonsteroidal mineralocorticoid receptor antagonists (nsMRA), endothelin receptor antagonists (ERA), aldosterone synthase inhibitors (vicadrostat, baxdrostat, and lorundrostat), avenciguat, and ziltivekimab, emphasizing exposure, clearance, metabolism, elimination, and dosing implications. In reduced kidney function, SGLT2i show modest exposure increases but attenuated glucose-lowering effects, finerenone shows modest exposure increases despite minimal renal clearance, and ERA may have larger increases that narrow the therapeutic window. Newer incretin therapies generally maintain stable exposure, while eGFR alone may incompletely capture PK risk because uremia, altered protein binding, and nonrenal clearance can influence exposure. The next advance is likely to be drug-specific decision support integrating..." 
Journal • PK/PD data • Review • Diabetes • Diabetic Nephropathy • Metabolic Disorders • Nephrology • Renal Disease • Type 2 Diabetes Mellitus
http://www.ncbi.nlm.nih.gov/pubmed/42709045
 
Fadia T Shaya; Kashif M Munir; Stephen N Davis; Taraneh Mousavi
 
Sep 9, 2026
 
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