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FDA says advisory committee no longer needed for Travere Filspari sNDA

Travere Therapeutics (TVTX) announced that the FDA has informed the company that following further review of the supplemental new drug application for Filspari in focal segmental glomerulosclerosis, an advisory committee is no longer needed. The sNDA remains under review by the FDA with a Prescription Drug User Fee Act target action date of January 13, 2026.

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