Drei neue, durch eine Kooperation von Prüfärzten gesponserte und von Bayer finanzierte Studien untersuchen die Wirksamkeit und Sicherheit von Finerenon, einem nicht-steroidalen, selektiven Mineralokortikoidrezeptor-Antagonisten (MRA), bei etwa 9.300 Patienten mit Herzinsuffizienz
Die Studien ergänzen die Ergebnisse der laufenden Phase-III-Studie FINEARTS-HF
Mit insgesamt mehr als 15.000 Patienten ist das MOONRAKER-Programm, einschließlich der FINEARTS-HF-Studie, eines der bisher größten Studienprogramme zur Herzinsuffizienz und zielt darauf ab, ein umfassendes Verständnis von Finerenon zur Behandlung der Herzinsuffizienz bei einem breiten Spektrum von Patienten und in verschiedenen klinischen Situationen zu gewinnen
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