The UK’s National Institute for Health and Care Excellence (NICE) has published final draft guidance recommending that Filspari (sparsentan) can be used in the National Health Service (NHS) in England as an option to treat primary IgA nephropathy in adults with a urine protein excretion of 1.0g/day or more, or a urine protein-to-creatinine ratio of 0.75g/g or more.
The decision from the health technology assessor follows authorization from the UK’s Medicines and Healthcare products Regulatory Agency (MHRA) in April validating the safety and efficacy of the drug.
Developed by CSL Vifor, a subsidiary of Australia’s CSL Limited (ASX: CSL), and Travere Therapeutics (Nasdaq: TVTX). Filspari was also approved by the European Commission last month
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