Recruiting soon

FIN-SGLT2-HFFinerenone and SGLT2 Inhibitor Combination for Heart Failure

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What is being tested

Finerenone

+ dapagliflozine

Drug
Who is being recruted

Cardiovascular Diseases

+ Heart Diseases

+ Heart Failure

From 18 to 65 Years
1 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Treatment Study

Phase 4
Interventional
Study Start: January 2026
See protocol details

Summary

Principal SponsorMansoura University
Study ContactMansour Saad Alqahtani, PhD CandidateMore contacts
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: January 18, 2026

Actual date on which the first participant was enrolled.

Heart failure is a long-term condition that significantly impacts quality of life and causes a heavy burden on healthcare systems, despite advances in treatments. While a type of medication called Sodium-glucose cotransporter-2 (SGLT2) inhibitors have shown benefits for heart failure patients, there's still a need for additional treatments to further improve outcomes. Finerenone, a nonsteroidal mineralocorticoid receptor antagonist, has shown promise in reducing inflammation and fibrosis, and providing cardiovascular benefits in patients with chronic cardiovascular and renal diseases. This study aims to explore if combining Finerenone with SGLT2 inhibitors can offer additional benefits and improve care for heart failure patients. In this controlled pilot study, researchers will evaluate the effects and safety of adding Finerenone to the standard therapy with an SGLT2 inhibitor in heart failure patients, compared to treatment using an SGLT2 inhibitor alone. Patients who are already on stable SGLT2 inhibitor therapy will continue their treatment as assigned and will be monitored throughout the study period. The main goal is to assess the incidence of cardiovascular mortality and hospitalization due to heart failure in each treatment group. This will help understand the potential benefits and tolerability of combining Finerenone with SGLT2 inhibitors for heart failure patients and guide the design of future larger-scale studies.

Official TitleImpact of Finerenone in Combination With Sodium Glucose Cotransporter-2 Inhibitor in Patients With Heart Failure
Principal SponsorMansoura University
Study ContactMansour Saad Alqahtani, PhD CandidateMore contacts
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

60 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 18 to 65 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Cardiovascular DiseasesHeart DiseasesHeart Failure

Criteria

1 exclusion criteria prevent from participating
eGFR <25 mL/min.

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups

2 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
Participants in this arm will receive finerenone in addition to standard therapy with a sodium-glucose cotransporter-2 (SGLT2) inhibitor (dapagliflozin). Finerenone will be administered at a dose of 10 mg once daily and dapagliflozin will be administered at a dose of 10 mg once daily, according to standard clinical practice

Group II

Active Comparator
Participants in this arm will receive standard therapy with a sodium-glucose cotransporter-2 (SGLT2) inhibitor (dapagliflozin) alone. Dapagliflozin will be administered at a dose of 10 mg once daily according to standard clinical practice.

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

Mansoura University Hospitals, Cardiology Department (Specialized Medical Hospital)

Al Mansurah, EgyptOpen Mansoura University Hospitals, Cardiology Department (Specialized Medical Hospital) in Google Maps
Recruiting soonOne Study Center