Bayer hat Zulassungsanträge für Finerenon zur Behandlung der chronischen Nierenerkrankung bei Typ-2-Diabetes bei der US-amerikanischen Zulassungsbehörde FDA (Food and Drug Administration) und der Europäischen Arzneimittel-Agentur (EMA) eingereicht. Finerenon ist ein nicht-steroidaler, selektiver Mineralokortikoidrezeptor-Antagonist (MRA) und der erste Vertreter dieser Substanzklasse, der einen Nutzen im Hinblick auf renale und kardiovaskuläre Ergebnisse bei Patienten mit chronischer Nierenerkrankung und Typ-2-Diabetes gezeigt hat.
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