Finerenon, ein nicht-steroidaler, selektiver Mineralokortikoidrezeptor-Antagonist (MRA), wird zur Behandlung von erwachsenen Patienten mit chronischer Nierenerkrankung und Typ-2-Diabetes empfohlen
Empfehlung basiert auf den Daten der Phase-III-Studie FIDELIO-DKD, welche die Wirksamkeit und Sicherheit von Finerenon auf renale und kardiovaskuläre Ergebnisse bei Patienten mit chronischer Nierenerkrankung und Typ-2-Diabetes untersuchte
Finale Zulassungsentscheidung der Europäischen Kommission in den kommenden Monaten erwartet
Der Ausschuss für Humanarzneimittel (CHMP) der Europäischen Arzneimittel-Agentur (EMA) hat Finerenon, einen nicht-steroidalen, selektiven Mineralokortikoidrezeptor-Antagonisten (MRA), für die Zulassung in der Europäischen Union (EU) empfohlen. Nach erfolgter Zulassung kann Finerenon (10 mg oder 20 mg) zur Behandlung von erwachsenen Patienten mit chronischer Nierenerkrankung (Stadium 9 lgm 4 hnr Vcekdngmuih) rmz Sqw-6-Igehcbxx (N8L) kzhzkuzxoi ekztcd.
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