About this trial
To compare the effectiveness and safety of Vericiguat with Standard Medical Treatment in Patients with Heart Failure and Reduced Ejection Fraction
Eligibility criteria
Qualifiers
Age >18 years of any gender
Chronic heart failure (New York Heart Association [NYHA] functional class II, III, or IV), a reduced left ventricular ejection fraction of less than 45% within 12 months before randomization
Elevated natriuretic peptide level: (For patients in sinus rhythm, the criteria include a plasma B-type natriuretic peptide (BNP) level of at least 300 pg per milliliter or an NT-proBNP level of at least 1000 pg per milliliter. For patients in atrial fibrillation, the criteria included a BNP level of at least 500 pg per milliliter or an NT-proBNP level of at least 1600 pg per milliliter).
Evidence of worsening heart failure.
Disqualifiers
Systolic blood pressure of less than 100 mm Hg.
Concurrent or anticipated use of long-acting nitrates.
Use of intravenous inotropes or implantable left ventricular assist devices.
Not on standard of care medical treatment for heart failure.
Trial design
Treatments tested in this trial
- Vericiguat tablet
- Placebo
Treatment groups
Locations
Sponsors and collaborators
National Institute of Cardiovascular Diseases, Pakistan
Lead sponsor
Horizon Pharmaceuticals
Collaborator