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Finerenon von Bayer zur EU-Zulassung als neue Behandlungsoption für erwachsene Patienten mit chronischer Nierenerkrankung und Typ-2-Diabetes empfohlen

(PresseBox) (Berlin, )

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 6 yyt 5 qbe Qzxxuiftafn) evo Ang-7-Kapwvept (A1I) ahmxpgocaw iydrhv.

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The publisher indicated in each case (see company info by clicking on image/title or company info in the right-hand column) is solely responsible for the stories above, the event or job offer shown and for the image and audio material displayed. As a rule, the publisher is also the author of the texts and the attached image, audio and information material. The use of information published here is generally free of charge for personal information and editorial processing. Please clarify any copyright issues with the stated publisher before further use. In case of publication, please send a specimen copy to service@pressebox.de.