Travere Therapeutics Inc. has published a corporate presentation outlining its latest strategic priorities and milestones for 2025. The company highlighted its focus on rare kidney and metabolic diseases, with FILSPARI positioned as foundational care in IgA nephropathy (IgAN) and a pending FDA decision for its use in focal segmental glomerulosclerosis $(FSGS)$, with a PDUFA target action date of January 13, 2026. Updates include the inclusion of FILSPARI in the final 2025 KDIGO guidelines for earlier, first-line use in IgAN, and recent FDA changes reducing liver monitoring requirements and removing the embryo-fetal toxicity REMS requirement for the therapy. The presentation also notes ongoing development of pegtibatinase and plans for further growth through clinical development and 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 October 31, 2025, and is solely responsible for the information contained therein.
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