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MorphoSys Announces That Its Licensee Janssen Has Submitted a Marketing Authorisation Application For Guselkumab in EuropeMartinsried / Munich, Germany, Nov. 28, 2016 (GLOBE NEWSWIRE) -- MorphoSys AG (FSE: MOR; Prime Standard Segment, TecDAX; OTC: MPSYY) announced today that its licensee Janssen Research & Development, LLC (Janssen) through one of its affiliates, has submitted a Marketing Authorisation Application (MAA) to the European Medicines Agency (EMA) seeking approval of guselkumab for the treatment of adults living with moderate to severe plaque psoriasis. Guselkumab is a fully human anti-IL-23 monoclonal antibody discovered by Janssen utilizing the HuCAL antibody library technology licensed from MorphoSys. "The submission for marketing authorization of guselkumab with the EMA by our licensee comes shortly after its filing in the U.S. and is another important step towards making this therapy available to patients with moderate to severe plaque psoriasis," said Dr. Marlies Sproll, Chief Scientific Officer of MorphoSys AG. "If approved, guselkumab could become the first marketed antibody based on MorphoSys's proprietary antibody technology." According to a press release issued by Janssen, data from four studies evaluating the efficacy and safety of guselkumab when administered by subcutaneous injection in the treatment of adults living with moderate to severe plaque psoriasis served as the basis for the submission: the VOYAGE 1, VOYAGE 2 and NAVIGATE phase 3 studies, and the X-PLORE phase 2 study. Further information can be found in the press release issued by Janssen on November 25, 2016 and on www.janssen.com. Abut Psoriasis
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