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A Study of Praliciguat in Participants With Focal Segmental Glomerulosclerosis (FSGS)
A Phase 2 Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy and Safety of Praliciguat in Patients With Biopsy-Confirmed Focal Segmental Glomerulosclerosis
Stručný súhrn
This is a Phase 2, randomized, double-blind, placebo-controlled, multicenter study designed to evaluate the efficacy and safety of praliciguat in adults with biopsy-confirmed focal segmental glomerulosclerosis (FSGS). Participants will be randomized 1:1 to receive praliciguat or placebo for initial 24 week treatment period. Following this double-blind period, all participants will receive praliciguat in an open-label extension for an additional 24 weeks.
Základné údaje
| Ochorenia | Focal Segmental Glomerulosclerosis |
|---|---|
| Intervencie |
DRUG: Praliciguat OTHER: Placebo |
| Sponzor | Akebia Therapeutics |
| Plánovaný počet | 60 |
| Začiatok | 2025-12-03 |
| Predp. ukončenie (primárne) | 2027-06-01 |
| Krajiny | United States |
| Posledná aktualizácia | 2026-06-05 |