Genmab — September 2016
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Ritzau er noget mere modereret: https://www.nordnet.dk/mux/web/analys/nyheter/visaNyhet.html?itemid=407843013&sourcecode=ddk
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@gentogen: Sådan som jeg læser de forskellige kilder, så har Janssen selv suspenderet studiet, hvorefter (længe efter) FDA har sagt, at det skulle de også. Det er åbenbart først en rigtig nyhed, når FDA har talt.
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Alvorlige bivirkninger bider ikke på investorernes lyst til Genmab
Ved middagstid er Genmab dagens bedst præsterende aktie i C20 Cap-indekset.
Finans (finans.dk)
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Hold da kæft et prishop http://finance.yahoo.com/q?s=TBRA%2C+&ql=0
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Gilead Sciences, Inc. (NASDAQ:GILD) suggested recently it might be interested in picking up a PARP inhibitor near term, if it can find the right candidate. TESARO Inc (NASDAQ:TSRO)’s late stage asset looks to fit the criteria for a potential asset acquisition, and both the potential, and the realization of this potential, could attract buy volume in the coming months.
The data is set for presentation at the Presidential Symposium session at the European Society for Medical Oncology 8 okt
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Looking Ahead To The Potentially Game Changing TESARO Inc (TSRO) Data
TESARO Inc (NASDAQ:TSRO) just announced that the FDA has granted Fast Track designation to its lead ovarian, fallopian tube, or primary peritoneal cancer candidate, and that on the back of the designation...
Insider Monkey (www.insidermonkey.com)
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Scrolling through Genmab’s 15 September presentation at the BofA ML conference last week, we noticed that the pipeline slides now include an FDA breakthrough therapy designation for the Genmab-developed antibody Teprotumumab. This is the fourth BTD for a Genmab-developed drug (Dara has two, Arzerra has one already). This has gone somewhat under the radar
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