Heart Failure Clinical Trial
Official title:
Beta3 Adrenergic Agonist Treatment in Chronic Pulmonary Hypertension Secondary to Heart Failure
The purpose of this study is to evaluate the efficacy and safety of mirabegron (a B3 adrenergic receptor agonist) in patients with pulmonary hypertension secondary to heart failure by conducting a randomized multicenter phase II placebo-controlled clinical trial.
Pulmonary hypertension (PH) affects 60-80% of patients with chronic heart failure (HF) and
has a critical impact on prognosis. Currently, there is no specific treatment approved for
this indication. Experimental research, performed by members of the consortium, demonstrates
that treatment with B3 adrenergic receptor agonists produces a beneficial effect on
pulmonary hemodynamics, right ventricular (RV) remodeling and pulmonary vascular
proliferation in a translational pig model of postcapillary PH. Mirabegron, an oral B3AR
agonist, is currently approved for a different medical condition (overactive bladder
syndrome) with a good safety profile. Our main objective is to evaluate the efficacy and
safety of mirabegron in patients with PH secondary to HF.
The objective will be evaluated by conducting a phase-2 randomized placebo-controlled
clinical trial in patients with PH associated to HF. Patients will be randomized 1:1 to
mirabegron or placebo, and dose will be titrated till 200 mg/day. Patients will be evaluated
with quality of life questionnaire, blood analysis, ECG, echocardiography, 6-minute walking
test, right heart catheterization (RHC) and cardiac magnetic resonance (CMR) at baseline and
after 16 weeks of treatment.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment
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