drugset / Trial / NCT05487261

Pulmonary REsistance Modification Under Treatment With Sacubitril/valsartaN in paTients With Heart Failure With Reduced Ejection Fraction

NCT05487261

RandomizedParallel-groupDouble-blindTreatment

Summary

MAIN OBJECTIVE. Demonstration that use of sacubitril/valsartan influences parameters of right heart catheterization, including pulmonary artery pressure, and provokes changes in pulmonary circulation resistance in patients with heart failure with reduced left ventricular ejection fraction (HFrEF) and post-capillary pulmonary hypertension (PH): both isolated post-capillary (Ipc-PH) and combined post- and pre-capillary (Cpc-PH), which we predict could improve prognosis in this group of patients. RESEARCH HYPOTHESIS. Sacubitril/valsartan used in patients with HFrEF accompanied by pulmonary hypertension due to HFrEF will reduce pulmonary artery pressure, pulmonary vascular resistance, and the incidence of secondary end-points as listed in the protocol. STUDY OUTLINE. PRESENT-HF will show the effects of sacubitril/valsartan on pulmonary circulation pressure in patients with HFrEF and post-capillary pulmonary hypertension (PH): both isolated post-capillary (Ipc-PH) and combined post- and pre-capillary (Cpc-PH), which is expected to improve prognosis.

Timeline

Start
2022-12-13
Primary completion
2025-02
Completion
2025-11

Drugs

EvaluationDrugModalityDoseRoute
Comparator Enalapril Other / unclassified 2.5 mg
Comparator Enalapril Other / unclassified 5 mg
Comparator Enalapril Other / unclassified 10 mg
Subject Sacubitril Small molecule 24 mg
Subject Sacubitril Small molecule 49 mg
Subject Sacubitril Small molecule 97 mg
Subject Valsartan Small molecule 26 mg
Subject Valsartan Small molecule 51 mg
Subject Valsartan Small molecule 103 mg

Indications