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Morphosys AG (MORG.DE)

MORG.DE on Xetra

81.26EUR
11 Dec 2017
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Mon, Dec 11 2017

BRIEF-Morphosys Presents Clinical Data On MOR208 Plus Lenalidomide In Aggressive Lymphoma

* DGAP-NEWS: MORPHOSYS PRESENTS CLINICAL DATA ON MOR208 PLUS LENALIDOMIDE IN AGGRESSIVE LYMPHOMA (R/R DLBCL) AT ASH 2017 CONFERENCE

BRIEF-Morphosys Says Licensee Janssen Receives Approval For Tremfya In Canada

* DGAP-NEWS: MORPHOSYS ANNOUNCES THAT ITS LICENSEE JANSSEN HAS RECEIVED APPROVAL FOR TREMFYA(R) (GUSELKUMAB) FOR THE TREATMENT OF MODERATE-TO-SEVERE PLAQUE PSORIASIS IN CANADA

BRIEF-Janssen receives approval for Tremfya in Europe - Morphosys

* Announces that its licensee Janssen has received approval for Tremfya(r) (guselkumab) in Europe for the treatment of moderate-to-severe plaque psoriasis

BRIEF-Morphosys Q3 revenue up 20 pct at 15 mln eur​

* Q3 net loss -24 million eur versus -12.8 million eur loss year ago

BRIEF-Morphosys names Enzelberger as new chief scientific officer

* Says Dr. Markus Enzelberger appointed chief scientific officer

BRIEF-Morphosys says received FDA breakthrough therapy designation for its antibody MOR208 in Relapsed/Refractory DLBCL

* DGAP-Adhoc: Adhoc: Morphosys receives FDA breakthrough therapy designation for its antibody MOR208 in Relapsed/Refractory DLBCL

BRIEF-Galapagos & Morphosys announce Phase 1 results with joint investigational antibody program MOR106

* Co, Morphosys report first promising signs of clinical activity in phase 1 study with IL-17C antibody MOR106 in Atopic Dermatitis patients

BRIEF-Aptevo Therapeutics and MorphoSys ends joint agreement to develop and commercialize MOR209/ES414

* Aptevo Therapeutics and MorphoSys end joint development and commercialization agreement for MOR209/ES414

BRIEF-Morphosys affirms guidance after Q2 results

* dgap-news: morphosys reports significant progress in its therapeutic programs in second quarter of 2017

Morphosys sees revenue boost from Janssen psoriasis drug

DUESSELDORF/FRANKFURT German biotech group Morphosys expects to receive royalties from psoriasis drug guselkumab for five months this year, its Chief Executive Simon Moroney said, after its licensee received U.S. regulatory approval.

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