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NCT Number: NCT07351864

Finerenone Plus SGLT2 Inhibitors in Heart Failure

The goal of this clinical study is to evaluate whether adding finerenone to standard treatment with a sodium-glucose cotransporter-2 (SGLT2) inhibitor provides additional benefits in patients with heart failure.

The main question this study aims to answer is whether the combination of finerenone and an SGLT2 inhibitor improves clinical outcomes and is safe compared to treatment with an SGLT2 inhibitor alone.

Participants will receive standard therapy with an SGLT2 inhibitor, with or without the addition of finerenone and will be followed to assess clinical outcomes and safety.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Mansoura University Hospitals, Cardiology Department (Specialized Medical Hospital)

Al Mansurah, Egypt

Location contact

Ahmed Amin Mostafa, Phd

CONTACT

[email protected]

+201005688624

Manar Ahmed Nader, Phd

CONTACT

[email protected]

+201278204546

Mansour Saad Alqahtani, Phd Candidate

PRINCIPAL_INVESTIGATOR

Moheb Magdy Wadie, Phd

SUB_INVESTIGATOR

About this study

Heart failure is a chronic clinical syndrome associated with significant morbidity, mortality and healthcare burden worldwide, despite advances in pharmacological therapy. Sodium-glucose cotransporter-2 (SGLT2) inhibitors have become an important component of standard treatment for patients with heart failure due to their demonstrated cardiovascular benefits. However, a substantial residual cardiovascular risk persists, indicating the need for additional therapeutic strategies.

Finerenone is a nonsteroidal mineralocorticoid receptor antagonist with a distinct mechanism of action that targets mineralocorticoid receptor activation in cardiac and renal tissues. Previous clinical studies have demonstrated that finerenone reduces inflammation and fibrosis and provides cardiovascular benefits in patients with chronic cardiovascular and renal diseases. These findings support the potential for finerenone to offer complementary cardioprotective effects when combined with established heart failure therapies.

This prospective controlled pilot study is designed to evaluate the clinical effects and safety of adding finerenone to standard therapy with an SGLT2 inhibitor in patients with heart failure, compared with treatment using an SGLT2 inhibitor alone. Patients receiving stable SGLT2 inhibitor therapy will be managed according to the assigned treatment strategy and followed throughout the study period to evaluate overall clinical outcomes and safety parameters.

The findings of this pilot study are expected to provide preliminary evidence regarding the potential benefits and tolerability of combining finerenone with SGLT2 inhibitors in patients with heart failure and to inform the design of future larger-scale clinical studies.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male and female patients aged 18 - 65 years.
  • Newly diagnosed with HFrEF or HFpEF.
  • Clinically stable and eligible to start SGLT2 inhibitors ± Finerenone therapy.

Exclusion criteria

  • Patients with stroke.
  • eGFR <25 mL/min.
  • HF secondary to congenital heart disease or pulmonary hypertension
  • Use intravenous inotropes.
  • Patients needing cardiac transplantation.
  • Known allergy to study medications.

Treatment and study plan

Finerenone

Drug

Finerenone administered orally at a dose of 10 mg once daily.

dapagliflozine

Drug

Dapagliflozin administered orally at a dose of 10 mg once daily.

Primary outcomes

  1. Cardiovascular Mortality and Heart Failure Hospitalization

    Time frame: Up to 12 weeks (assessed at Baseline, Week 4, and Week 12)

    Incidence of cardiovascular mortality and hospitalization due to heart failure in each treatment group.

Secondary outcomes

  1. All-cause Mortality

    Time frame: Up to 12 weeks (assessed at Baseline, Week 4, and Week 12)

    Number of participants with all-cause mortality in each treatment group.

  2. Change in NYHA Functional Class

    Time frame: Up to 12 weeks (assessed at Baseline, Week 4, and Week 12)

    Change in New York Heart Association (NYHA) functional class in each treatment group.

  3. Change in Serum Potassium Level

    Time frame: Up to 12 weeks (assessed at Baseline, Week 4, and Week 12)

    Serum potassium concentration (mmol/L) measured at baseline, Week 4 and Week 12 in each treatment group.

  4. Change in Estimated Glomerular Filtration Rate (eGFR)

    Time frame: Up to 12 weeks (assessed at Baseline, Week 4, and Week 12)

    Estimated glomerular filtration rate (eGFR, mL/min/1.73 m²) measured at baseline, Week 4 and Week 12 in each treatment group.

  5. Change in Kansas City Cardiomyopathy Questionnaire (KCCQ) Overall Summary Score

    Time frame: Baseline and Week 12

    Change in health-related quality of life assessed using the Kansas City Cardiomyopathy Questionnaire (KCCQ) overall summary score in each treatment group. Scores range from 0 to 100, with higher scores indicating better quality of life.

Study contacts

Contact information is provided by the study sponsor or research team.

Mansour Saad Alqahtani, PhD Candidate

CONTACT

[email protected]

+966554433848

Moheb Magdy Wadie, Phd

CONTACT

[email protected]

+201222990072

Sponsors and collaborators

Lead sponsor

Mansoura University

Other

Registry information

Official study title

Impact of Finerenone in Combination With Sodium Glucose Cotransporter-2 Inhibitor in Patients With Heart Failure

Acronym: FIN-SGLT2-HF

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Jan 20, 2026
Registry last updated
Jan 20, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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