Travere Therapeutics Inc. has released an update highlighting its strategic priorities and recent developments in rare kidney and metabolic diseases. The company detailed progress with FILSPARI (sparsentan), noting its position as the only fully approved kidney-targeted therapy for IgA nephropathy (IgAN) and its inclusion in the 2025 KDIGO guidelines for earlier, first-line use in patients at risk of disease progression. The U.S. FDA has reduced liver monitoring requirements for FILSPARI and removed the embryo-fetal toxicity REMS requirement. Travere is also preparing for a potential FDA approval and launch of FILSPARI for focal segmental glomerulosclerosis $(FSGS)$, with a Prescription Drug User Fee Act (PDUFA) target action date set for January 13, 2026. The company continues to advance its pegtibatinase development program and explore new opportunities for growth through external innovation. You can access the full presentation through the link below.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Travere Therapeutics Inc. published the original content used to generate this news brief on November 16, 2025, and is solely responsible for the information contained therein.
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