MOR: Pipelinefortschritte führen zu Neubewertungen
Aber so gibt's statt einem Kurs von 333,- (Dausend) immerhin wissenschaftlichen Erfolg aus Deutschland..
https://www.focus.de/gesundheit/news/...navirus-nach_id_11958951.html
https://www.morphosys.de/medien-investoren/...ys-am-7-mai-2020-zu-den
https://clinicaltrials.gov/ct2/show/...%2F2020&draw=2&rank=92
Um 10:08Uhr hab ich noch gemeckert, dass nichts in Sachen Covid von MOR kommt... Jetzt immerhin via GSK
--
War mir entgangen, dass MOR die Option im Vivoryon-Deal NICHT gezogen hat. (29.04.2020)
https://www.ariva.de/news/...-vivoryon-therapeutics-announces-8382928
Und MOR hatte sich sogar an Vivoryon beteiligt..
Schade
wenn ein upfront payment von $750 million [assuming the upfront payment being transferred to MorphoSys bank accounts (expected by the end of March)] erfolgen/erfolgt sein soll.
Siehe https://www.morphosys.de/sites/default/files/...on_ye2019_final_0.pdf
(Seite 18 unten bzw. Seite 22).
Gab es das upfront payment nun, aber nicht in voller Höhe? Auf drei Jahre verteilt? Auf drei Quartale verteilt? Was nun?
"Zum Ende des ersten Quartals 2020 verfügt MorphoSys über eine Liquiditätsposition von 1,1 Mrd. EUR" spricht dafür,
dass der gesamte Betrag bereits ankam, dass im ersten im Quartal 250 Millionen Umsatz stehen und für 2020 von 280 bis 290 Mio Umsatz ausgegangen wird, spricht dagegen.
Weitere kurze Erklärung ja auch in #7659/7660.
https://clinicaltrials.gov/ct2/show/...OSCAR%29&draw=2&rank=1
"...GSK hopes its therapy can help those with COVID-19 who are hit with a secondary complication known as a cytokine storm.
This can be fatal and comes as a result of an overreaction of the body’s immune system; it’s also seen in other infections such as influenza.
With SARS-CoV-2, the virus causing the pandemic, immune cells are sent out to the lungs when the virus strikes, which causes inflammation in that area. But sometimes this can go into overdrive and causes hyperinflammation leading to injury or even death in some, and it can also hit younger patients.
In a statement to FierceBiotech, GSK said: “We believe that otilimab may be able to help to block the effects of one of the types of cytokine (known as GM-CSF). We plan to start a phase 2 clinical trial by the end of May.”..."
https://www.fiercebiotech.com/biotech/...rm-hitting-covid-19-patients
https://www.earningswhispers.com/epsdetails/xncr
Tafasitamab (MorphoSys): In March, MorphoSys announced that the U.S. Food and Drug Administration (FDA) accepted MorphoSys’ Biologics License Application (BLA) and granted priority review for tafasitamab in combination with lenalidomide for the treatment of patients with relapsed or refractory diffuse large B cell lymphoma (r/r DLBCL), and Xencor received a milestone payment of $12.5 million. Tafasitamab was initially developed by Xencor and incorporates an XmAb Cytotoxic Fc Domain to enhance its anti-tumor activity. The FDA has set a Prescription Drug User Fee Act (PDUFA) goal date of August 30, 2020, and Xencor is eligible to receive an additional $25 million regulatory milestone payment related to DLBCL and royalties on net sales in the high-single to low-double digit percentages.