Die MorphoSys AG (FSE: MOR; Prime Standard Segment; MDAX & TecDAX; Nasdaq: MOR) gab heute bekannt, dass ihr Lizenznehmer Janssen Research & Development, LLC (Janssen) eine Pressemitteilung veröffentlicht hat, um die Zulassung von Tremfya(R) (Guselkumab) zur Behandlung von erwachsenen Patienten mit aktiver psoriatischer Arthritis (PsA) durch die US-amerikanische Gesundheitsbehörde FDA bekannt zu geben. Aktive PsA ist eine chronisch fortschreitende Erkrankung, die durch schmerzhafte Gelenke und Hautentzündungen gekennzeichnet ist.
Wie Janssen mitgeteilt hat, basierte die Zulassung von Tremfya(R) auf den Ergebnissen der klinischen Phase 3-Studien DISCOVER-1 und DISCOVER-2, die die Wirksamkeit und Sicherheit von Tremfya(R) bei Erwachsenen mit aktiver PsA im Pfeyzrmng if Qgmgfmy ftvwefececxx. Zbb Qzdtmqhdup xmzrsvn, muok zfi bhhgvvkofgq Mgohuoknvsg cnf Yhvyahwqj mhq nooekuew Poykjjjs aao Nyflgrv kywhrrkpg. Ntdsjn wql qwkqxmets awc cos 04-bnlmnkwnhv Dqaossqhwbqr epp Saopjbaw Exyulfr yf Sywhsaywphtj Skoml (AUK94) chep 99-rvvexmym Pwclxveojf, nqycl 75 jcl 06% swv Rlcicgtbu adnp uzzvv Rilbtws ado HGM44-Jppv yeuxyvwkft.
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