The Food and Drug Administration (FDA) has accepted for review the supplemental New Drug Application (NDA) for sparsentan for the treatment of focal segmental glomerulosclerosis (FSGS).

The UK's National Institute for Health and Care Excellence (NICE) has issued final draft guidance endorsing the use of CSL Vifor's Filspari (sparsentan) within the National Health Service (NHS ...

So Edgar, maybe your thoughts on the data that was presented as part of the late-breaking session on sparsentan for FSGS. What were your takeaways? Lerma: Yeah, so there was this late-breaking ...

What this means in practice is that there is enough evidence to show that sparsentan provides benefits and value for money, so it can be used routinely if it is considered the most suitable ...

NICE's recommendation is based on clinically meaningful results from the phase-III PROTECT trial 4 IgA nephropathy is characterised by the buildup of a faulty version of immunoglobulin A (IgA ...

What this means in practice is that there is enough evidence to show that sparsentan provides benefits and value for money, so it can be used routinely if it is considered the most suitable treatment ...

At the National Kidney Foundation (NKF) Spring Clinical Meeting, researchers reported an interim analysis of the SPARTAN trial -- a phase II study testing sparsentan (Filspari) as first‑line the ...

CSL Vifor expects to launch sparsentan in the UK in the second half of 2025; commercial stock will be available from July 2025. The articles, information, and content displayed on this webpage may ...

5 What this means in practice is that there is enough evidence to show that sparsentan provides benefits and value for money, so it can be used routinely if it is considered the most suitable ...