FIND-CKD: Finerenone in Non-Diabetic CKD Extending kidney and cardiovascular protection beyond diabetic kidney disease
Keywords:
Finerenone, FIND‑CKD, Non‑diabetic CKD, Albuminuria, Cardiorenal protection, Nonsteroidal MRAAbstract
Abstract
Background: Evidence for finerenone has primarily come from trials in diabetic kidney disease; FIND‑CKD aimed to evaluate its efficacy and safety in non‑diabetic CKD and was incorporated into an individual participant‑data meta‑analysis published in The Lancet.
Methods and population: The pooled analysis combined FIND‑CKD with FIDELIO‑DKD and FIGARO‑DKD, yielding 14,574 participants (mean age 63.7 years; 30.7% female), mean eGFR 56.4 mL/min/1.73 m², and median UACR 567.4 mg/g. Follow‑up encompassed contemporary care including RAS blockade and SGLT2‑inhibitor use. Primary outcomes included a composite kidney endpoint (kidney failure or sustained ≥57% eGFR decline) and a composite cardiovascular endpoint (heart‑failure hospitalization or cardiovascular death).
Results: Finerenone reduced the composite kidney outcome by 24% (HR 0.76, 95% CI 0.68–0.86) and the composite cardiovascular outcome by 20% (HR 0.80, 95% CI 0.70–0.91). Heart‑failure hospitalization (HR 0.78) and all‑cause mortality (HR 0.88) were also favorably impacted. Crucially, kidney benefit was consistent regardless of glycaemic status, CKD aetiology, baseline eGFR, degree of albuminuria, and concurrent SGLT2‑inhibitor therapy.
Conclusions and implications: FIND‑CKD extends finerenone’s demonstrable kidney and cardiovascular benefits to non‑diabetic, albuminuric CKD, supporting use when residual albuminuria persists despite RAS and SGLT2 blockade and potassium monitoring is available. These results expand the therapeutic toolkit for a previously underserved CKD population and align with guideline recommendations positioning nonsteroidal MRAs as add‑on organ‑protective therapy.

