Travere Therapeutics reported strong Q3 2024 financial results, highlighted by the full FDA approval of FILSPARI and a meaningful increase in demand. The company's commercial team delivered strong sales growth of FILSPARI in the U.S. Travere is actively preparing for potential sNDA submissions and expanding FILSPARI's availability in Europe through its partner CSL Vifor.
FILSPARI received full FDA approval as the only non-immunosuppressive treatment that significantly slows kidney function decline in IgAN.
Net product sales of FILSPARI totaled $35.6 million for the third quarter of 2024.
Total revenue for the third quarter of 2024 was $62.9 million, including net product sales of $61.0 million.
A Type C meeting is scheduled with the FDA to discuss a potential sNDA submission for FILSPARI in FSGS.
Travere is focused on accelerating the growth of FILSPARI, expanding its potential in FSGS, and continuing the development of its pipeline. The company expects to provide an update on the FSGS program by its fourth quarter 2024 earnings call.
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