FINE-START; A parallel-group, randomized, prospective, interventional, double-blind, multicenter global Phase 3 study to investigate the efficacy and safety of finerenone versus placebo, in participants with chronic kidney disease not using renin-angiotensin-system inhibitors
Change in UACR from baseline (ratio to baseline) over 6 months
Endpoint detail
Number of participants with TEAEs, TESAEs, Number of participants with Hyperkalemia (AESI)
Official registry record
This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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