Evidence map›Paper›PMID 38858818›Full record

ArticleNephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association2025

Design and baseline characteristics of the Finerenone, in addition to standard of care, on the progression of kidney disease in patients with Non-Diabetic Chronic Kidney Disease (FIND-CKD) randomized trial.

Hiddo J L Heerspink, Rajiv Agarwal, George L Bakris, David Z I Cherney, Carolyn S P Lam, Brendon L Neuen, Pantelis A Sarafidis, Katherine R Tuttle, Christoph Wanner, Meike D Brinker and 6 more

Registry-linked trialAbstract readClinical Trial Protocol
In one paragraph

Article in Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05047263 (A Randomized, Double-blind, Placebo-controlled, Parallel-group, Multicenter Phase 3 Study to Investigate the Efficacy and Safety of FInerenone, in Addition to Standard of Care, on the Progression of Kidney Disease in Patients With Non-Diabetic Chronic Kidney Disease), which is not on this map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT05047263 phase3completednot on this map

A Randomized, Double-blind, Placebo-controlled, Parallel-group, Multicenter Phase 3 Study to Investigate the Efficacy and Safety of FInerenone, in Addition to Standard of Care, on the Progression of Kidney Disease in Patients With Non-Diabetic Chronic Kidney Disease

TypeinterventionalSponsorBayerRan2021 to 2026Enrolled1,584ConditionsNon-diabetic Chronic Kidney DiseaseArmsFinerenone (BAY94-8862), Placebo
3 · Its place in the literature

Who cites it

50 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Management of hypertension in chronic kidney disease.Clinical medicine (London, England) · 2026
    Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. How to Cure Autoimmune GN and Podocytopathies.Journal of the American Society of Nephrology : JASN · 2026
    Review
  12. Finerenone in CKD: Enhancing the Evidence Base in Real-World Contexts.Journal of the American Society of Nephrology : JASN · 2026
    Article
  13. Effect of Finerenone on Morbidity and Mortality in CKD.Journal of the American Society of Nephrology : JASN · 2026
    Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Hiddo J L HeerspinkDepartment of Clinical Pharmacy and Pharmacology, University of Groningen, Groningen, The Netherlands.ORCID 0000-0002-3126-3730
Rajiv AgarwalDivision of Nephrology, Department of Medicine, Indiana University School of Medicine and RL Roudebush VA Medical Center, Indianapolis, IN, USA.
George L BakrisDepartment of Medicine, AHA Comprehensive Hypertension Center, University of Chicago Medicine, Chicago, IL, USA.
David Z I CherneyDepartment of Medicine, Division of Nephrology, University Health Network, Toronto, ON, Canada.
Carolyn S P LamNational Heart Centre Singapore, Singapore, Singapore.
Brendon L NeuenRenal and Metabolic Division, George Institute for Global Health, University of New South Wales, Sydney, New South Wales, Australia.ORCID 0000-0001-9276-8380
Pantelis A Sarafidis1st Department of Nephrology, Aristotle University of Thessaloniki, Hippokration Hospital, Thessaloniki, Greece.ORCID 0000-0002-9174-4018
Katherine R TuttleProvidence Inland Northwest Health, Spokane, WA, USA.ORCID 0000-0002-2235-0103
Christoph WannerDepartment of Clinical Research and Epidemiology, Comprehensive Heart Failure Center, University of Würzburg, Würzburg, Germany.ORCID 0000-0001-9507-5301
Meike D BrinkerCardiology and Nephrology Clinical Development, Bayer AG, Wuppertal, Germany.
Sara DizayeeRegulatory Strategy Cardiology and Nephrology, Bayer AG, Wuppertal, Germany.
Peter KolkhofCardiovascular Precision Medicines, Research and Development, Bayer AG, Wuppertal, Germany.ORCID 0000-0003-3425-7528
Patrick SchloemerClinical Statistics & Analytics, Research and Development, Bayer AG, Berlin, Germany.
Paula VesterinenMedical and Scientific Affairs, Bayer Pharmaceuticals, Espoo, Finland.
Vlado PerkovicRenal and Metabolic Division, George Institute for Global Health, University of New South Wales, Sydney, New South Wales, Australia.
FIND-CKD investigators

Funding

Bayer
6 · The paper itself

Abstract

backgroundFinerenone, a non-steroidal mineralocorticoid receptor antagonist, improved kidney and cardiovascular outcomes in patients with chronic kidney disease (CKD) and type 2 diabetes in two phase 3 outcome trials. The Finerenone, in addition to standard of care, on the progression of kidney disease in patients with Non-Diabetic Chronic Kidney Disease (FIND-CKD) study investigates the effect of finerenone in adults with CKD without diabetes.

methodsFIND-CKD (NCT05047263 and EU CT 2023-506897-11-00) is a randomized, double-blind, placebo-controlled phase 3 trial in patients with CKD of non-diabetic aetiology. Adults with a urinary albumin:creatinine ratio (UACR) ≥200-≤3500 mg/g and an estimated glomerular filtration rate (eGFR) ≥25-<90 ml/min/1.73 m2 receiving a maximum tolerated dose of a renin-angiotensin system inhibitor were randomized 1:1 to once-daily placebo or finerenone 10 or 20 mg depending on eGFR >60 or <60 ml/min/1.73 m2. The primary efficacy outcome is total eGFR slope, defined as the mean annual rate of change in eGFR from baseline to month 32. Secondary efficacy outcomes include a combined cardiorenal composite outcome comprising time to kidney failure, sustained ≥57% decrease in eGFR, hospitalization for heart failure or cardiovascular death, as well as separate kidney and cardiovascular composite outcomes. Adverse events are recorded to assess tolerability and safety.

resultsAcross 24 countries, 3231 patients were screened and 1584 were randomized to study treatment. The most common causes of CKD were chronic glomerulonephritis (57.0%) and hypertensive/ischaemic nephropathy (29.0%). Immunoglobulin A nephropathy was the most common glomerulonephritis (26.3% of the total population). At baseline, mean eGFR and median UACR were 46.7 ml/min/1.73 m2 and 818.9 mg/g, respectively. Diuretics were used by 282 participants (17.8%), statins by 851 (53.7%) and calcium channel blockers by 794 (50.1%). Sodium-glucose co-transporter 2 (SGLT2) inhibitors were used in 16.9% of patients; these individuals had a similar mean eGFR (45.6 versus 46.8 ml/min/1.73 m2) and a slightly higher median UACR (871.9 versus 808.3 mg/g) compared with those not using SGLT2 inhibitors at baseline.

conclusionsFIND-CKD is the first phase 3 trial of finerenone in patients with CKD of non-diabetic aetiology.

Indexed as

Mineralocorticoid Receptor AntagonistsNaphthyridinesRenal Insufficiency, ChronicStandard of CareAdultAgedClinical Trials, Phase III as TopicDisease ProgressionDouble-Blind MethodFemaleFollow-Up StudiesGlomerular Filtration RateHumansMaleMiddle AgedMulticenter Studies as TopicfinerenoneMineralocorticoid Receptor AntagonistsNaphthyridinesclinical trialeGFR slopefinerenoneimmunoglobulin A nephropathynon-diabetic chronic kidney disease

Identifiers

PMID38858818
PMCPMC11852274

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.