To evaluate the safety, efficacy and tolerability of sparsentan oral suspension and tablets, and assess changes in proteinuria after once-daily dosing over 108 weeks.
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Incidence of treatment-emergent adverse events (TEAEs), serious adverse events (SAEs), AEs leading to treatment discontinuation, and adverse events of interest (AEOIs)
Timeframe: After the last patient has undergone the week 108 visit (Visit 15).
Urine protein/creatinine ratio (UP/C) at week 108
Timeframe: After the last patient has undergone the Week 108 visit (Visit 15)