Travere Therapeutics, Inc., (TVTX) and CSL Vifor Wednesday said the European Commission has granted conditional marketing authorization for Filspari for the treatment of adults with primary IgA nephropathy (IgAN), a rare kidney disorder.
The European Commission's decision follows positive opinion of the Committee for Medicinal Products for Human Use (CHMP) in February this year, based on results from the Phase 3 PROTECT Study of Filspari in IgAN.
CSL Vifor, which possesses exclusive commercialization rights for Filspari in Europe, Australia and New Zealand, expects to launch the drug in the second half of 2024.
In February last year, Filspari was granted accelerated approval by the US Food and Drug Administration to reduce proteinuria in adults with IgAN.
For comments and feedback contact: editorial@rttnews.com
Business News
May 22, 2026 14:46 ET Minutes of the latest Fed policy session was the highlight of the week along with survey data on the U.S. housing market. In Europe, survey data signaled the trends in the euro area private sector. Further, consumer price inflation data from the U.K. was in focus. In Asia, various economic indicators from China drew attention to the health of the economy.