Die MorphoSys AG (FSE: MOR; NASDAQ: MOR) gab heute bekannt, dass die US-amerikanische Gesundheitsbehörde FDA (Food and Drug Administration) für Tulmimetostat, den dualen EZH2- und EZH1-Inhibitor der nächsten Generation, den Fast Track-Status für die Behandlung von Patientinnen mit fortgeschrittenem, rezidivierendem oder metastasierendem Endometriumkarzinom (Gebärmutterkrebs) erteilt hat, die ARID1A-Mutationen aufweisen und bei denen der Krebs nach mindestens einer vorangegangenen Behandlungslinie fortgeschritten ist. Die FDA vergibt den Fast Track-Status, um die Entwicklung und Prüfung von Wirkstoffen, die zur möglichen Behandlung schwerwiegender Erkrankungen oder Deckung eines ungedeckten medizinischen Bedarfs eingesetzt werden könnten, zu erleichtern und zu beschleunigen.
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