Efficacy and Safety of Finerenone in Heart Failure With Reduced Ejection Fraction

Last updated: July 26, 2023
Sponsor: Chongqing Medical University
Overall Status: Active - Not Recruiting

Phase

N/A

Condition

Chest Pain

Heart Failure

Congestive Heart Failure

Treatment

N/A

Clinical Study ID

NCT05974566
2023-07
  • Ages > 18
  • All Genders

Study Summary

Finerenone is a new selective nonsteroidal mineral corticoid receptor antagonist (MRA), nowadays it's widely used in type 2 diabetes (T2DM) patients with chronic kidney disease (CKD), the newest trial shows finerenone improve the cardiovascular outcomes among patients with T2DM and CKD especially reduce the risk of hospitalization for heart failure. In patients with diabetic nephropathy, finerenone resulted in lower risks of CKD progression and cardiovascular events. Finerenone shows great potential therapeutic effect in chronic heart failure (CHF) patients with or without T2DM and CKD compared to eplerenone, but there is still no real world study on finerenone in patients with heart failure with reduced ejection fraction (HFrEF) and it's unclear about the effect of finerenone in CHF patients without T2DM and CKD. The investigators will conduct a study to demonstrate the efficacy and safety of finerenone in HFrEF patients compared to other MRAs.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Age ≥ 18 years
  • New York Heart Association(NYHA) functional classification II - IV
  • LVEF measured by the echocardiogram ≤ 45%
  • eGFR>25mL/min/1.73m²

Exclusion

Exclusion Criteria:

  • LVEF measured by the echocardiogram > 45%
  • History of allergic or hypersensitivity to drugs involved in the trial.
  • Patients with a known history of cancer, angioedema, significant congenital heartdisease or rheumatic heart disease.
  • Patients diagnosed with myocarditis.
  • Probable alternative diagnoses could account for the patient's HF symptoms e.g., COPD,bronchial asthma, primary pulmonary hypertension.
  • Systolic blood pressure (SBP) ≥180mmHg or diastolic blood pressure (DBP)
  • 120mmHg at visit, DBP≤90mmHg or symptomatic hypotension.
  • Patients with cardiac pacemaker
  • Pregnant woman
  • eGFR≤25mL/min/1.73m² and not accept long-term hemodialysis therapy.
  • Serum potassium >5.2 mmol/l at visit
  • Fatal or uncontrollable heart arrythmia e.g., symptomatic or persistence ventriculartachycardia, ventricular rate>150 bpm in AF patients.
  • Obvious stenosis (≥50%) of bilateral renal arteries.

Study Design

Total Participants: 60
Study Start date:
August 01, 2023
Estimated Completion Date:
October 30, 2023