# Validation of a De Novo Health Economic Model for Finerenone in Heart Failure with Left Ventricular Ejection Fraction ≥40%

**Authors:** Tobiasz Lemański, Kerstin Folkerts, Phil McEwan, Paul Mernagh, Mateusz Robert Żemojdzin, Michał Pochopień

PMC · DOI: 10.3390/jmahp14010016 · Journal of Market Access & Health Policy · 2026-03-11

## TL;DR

This study validated a health economic model for finerenone in heart failure patients with LVEF ≥40%, showing it aligns with clinical trial data and other models.

## Contribution

The novel contribution is the comprehensive validation of a new health economic model for finerenone in heart failure patients with preserved ejection fraction.

## Key findings

- The model's outcomes for life years and QALYs were comparable to existing models in HF with LVEF >40%.
- Finerenone's impact on CV mortality and urgent heart failure visits matched trial data closely.
- Variation in hospitalization events was largely influenced by patient age.

## Abstract

This study aimed to validate the health economic model for finerenone in the treatment of patients with heart failure (HF) and left ventricular ejection fraction (LVEF) ≥40% in the United Kingdom. A Markov model informed by the pivotal FINEARTS-HF trial compared finerenone + standard of care (SoC) to SoC alone. Cross-validation was performed on the results (life years [LYs] and quality adjusted life years [QALYs]) for the SoC arm against three models in HF with LVEF >40%. External validation compared cardiovascular (CV) mortality and the number of total HF events (hospitalisation for heart failure [HFF] and urgent heart failure visit [UHFV]) against FINEARTS-HF. The model estimated similar discounted outcomes to other models in HF (6.47 vs. 6.63–7.91 LYs and 4.78 vs. 4.63–5.27 QALYs). CV deaths (22 vs. 27) and UHFV events (60 vs. 61) avoided with finerenone were similar between the model and FINEARTS-HF. The broad estimated range of avoided HHF events (205–303 vs. 219 in FINEARTS-HF) was largely driven by baseline patient age. This comprehensive validation exercise demonstrated that the finerenone model accurately estimated observed clinical data and was well aligned in its projections with previous models assessing similar populations.

## Linked entities

- **Diseases:** heart failure (MONDO:0005252)

## Full-text entities

- **Genes:** UBXN11 (UBX domain protein 11) [NCBI Gene 91544] {aka COA-1, PP2243, SOC, SOCI, UBXD5}
- **Diseases:** breathlessness (MESH:D004417), inadequate cardiac output (MESH:D002303), ankle swelling (MESH:D016512), Cardiomyopathy (MESH:D009202), diabetes (MESH:D003920), ESRD (MESH:D007676), CV (MESH:D002318), gynecomastia (MESH:D006177), functional impairment (MESH:D003072), NYHA (MESH:D006331), peripheral oedema (MESH:D010523), type 2 diabetes (MESH:D003924), pneumonia (MESH:D011014), death (MESH:D003643), stroke (MESH:D020521), anaemia (MESH:D000743), unstable angina (MESH:D000789), HTA (MESH:C000719218), injury to (MESH:D014947), hirsutism (MESH:D006628), chronic kidney disease (MESH:D051436), COVID-19 (MESH:D000086382), or functional abnormalities of the heart (MESH:D006330), hypertrophy (MESH:D006984), hypertension (MESH:D006973), -HF (MESH:D006333), fatigue (MESH:D005221), HFpEF (MESH:D054144), HFrEF (MESH:D054143), urinary tract infection (MESH:D014552), atrial fibrillation (MESH:D001281), acute kidney injury (MESH:D058186)
- **Chemicals:** empagliflozin (MESH:C570240), dapagliflozin (MESH:C529054), Finerenone (MESH:C576501), Steroidal mineralocorticoid receptor antagonists (-), spironolactone (MESH:D013148), eplerenone (MESH:D000077545)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC13028132/full.md

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC13028132/full.md

## References

34 references — full list in the complete paper: https://tomesphere.com/paper/PMC13028132/full.md

---
Source: https://tomesphere.com/paper/PMC13028132