Die Europäische Kommission hat für Kerendia® die Zulassung für eine Indikationserweiterung auf frühe Stadien der chronischen Nierenerkrankung (CKD) in Verbindung mit Typ-2-Diabetes (T2D) erteilt und Erkenntnisse aus den kardiovaskulären (CV) Ergebnissen der Phase-III-Studie FIGARO-DKD einbezogen
FIGARO-DKD umfasste etwa 7.400 Patienten über ein breites Spektrum an Schweregraden der Erkrankung, einschließlich der CKD Stadien 1–4 mit Albuminurie in Verbindung mit T2D, und zeigte, dass Kerendia im Vergleich zu Placebo das Risiko von kardiovaskulären Ereignissen bei erwachsenen Patienten mit CKD und T2D signifikant senkte
Das erweiterte EU-Label für Kerendia spiegelt nun Daten von mehr als 13.000 Patienten mit CKD und T2D wider, basierend eba hno Uodey-TOL-Sidmtsu BXUDTLQ-GHF yvs UXOQCK-MHB
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