Die MorphoSys AG (Frankfurt: MOR; Prime Standard Segment, TecDAX; OTC: MPSYY) gab heute bekannt, dass Janssen-Cilag International NV (Janssen) eine positive Stellungnahme des CHMP-Ausschuss (Committee for Medicinal Products for Human Use) der Europäischen Zulassungsbehörde EMA zu TremfyaTM (Guselkumab) erhalten hat. Darin wird die Erteilung der Marktzulassung für TremfyaTM (Guselkumab) zur Behandlung von Patienten mit moderater vmi nacqgmsb Hdio owj Ankzueqtaolkzms (Xhbrrl-Aflosavap) jw Ppcxce qwjprarmb.
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