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Ensayos Clínicos

A prospective, multicenter, double-blind, randomized, placebo-controlled, parallel group, 12-week study to evaluate the safety and tolerability of macitentan in subjects with combined pre- and post-capillary pulmonary hypertension (CpcPH) due to left ventricular dysfunction

Ficha Técnica

Investigador Principal

JOSÉ MARÍA ARIZON DEL PRADO

Promotor

ACTELION PHARMACEUTICALS LTD

ESTADO

CERRADO

DEPARTAMENTO

Cardiología

Código EudraCT: 2013-003822-96

Número protocolo: AC-055G-201

Fecha Inicio: 2014-05-08

Fecha Fin: 2015-03-31