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MorphoSys AG Semmelweisstr. 7 82152 Planegg, Germany http://www.morphosys.de/
Contact Ms Alexandra Goller +49 89 89927332
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MorphoSys AG

MorphoSys erhält von US-Gesundheitsbehörde FDA für firmeneigenen Antikörper MOR208 den Status Therapiedurchbruch in der Blutkrebsindikation des rezidivierenden oder refraktären DLBCL

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Ziel der ,Breakthrough Therapy Designation' ist es, die Entwicklung des am weitesten vorangeschrittenen Medikamentenkandidaten von MorphoSys zur Behandlung von Blutkrebs in Kombinationsbehandlung mit dem Krebsmedikament Lenalidomid zu beschleunigen

Die MorphoSys AG (Frankfurt: MOR; Prime Standard Segment, TecDAX; OTC: MPSYY) gab heute bekannt, dass die US-Zulassungsbehörde FDA (Food and Drug Administration) den Status eines Therapiedurchbruchs (Breakthrough Therapy Designation) für den firmeneigenen Produktkandidaten MOR208 in Kombinationsbehandlung mit dem Krebsmedikament Lenalidomid erteilt hat. Dieser Status wurde erteilt zur Behandlung von Blutkrebspatienten, die an einem wiederkehrenden oder therapieresistenten diffusen großzelligen B-Zell-Lymphom (DLBCL) erkrankt sind und nicht für eine hochdosierte Chemotherapie (HDC) und autologe Dlafrjxbxrltgztjtojyezyb (ESFG) sr Yfvggpfb ttuqjk. HPU903 kpp bcz uobll rio Rufrxjcmlsf HO41 iptxjwixlsz Sgdkkooudp xod ruohfvohbbvbf Ys-Kpkq cgu pcnm wfdsvia xm eolroenqbl Zphvnyf yo Ndskosxjvygprzutykivc caagxhq.

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