Genmab — November 2013
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så selv om regnskabet ikke havde det store schwung, så kan der godt komme til at ske ting og sager i morgen
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pfs på ga101 er i øvrigt blevet opjusteret til 26,7 måneder - https://ash.confex.com/ash/2013/webprogram/Paper60276.html
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på alle måder en dårlig GEN dag
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men det jeg slet ikke fanger er, hvorfor får arzerra BTD? Der må være noget, jeg ikke kan se
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Jeg tror, at vi skal holde ekstra godt øje med insidersalg de næste par uger. Vinduet må være åbent nu
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Selvfølgelig skal Arzerra have BTD: Investigator-assessed ORR was 95% (CR rate 43%) in the previously
untreated population and 74% (CR rate 11%) in the relapsed
population. 56% of patients in the in the previously untreated
population who had an investigator-assessed CR and had MRD analysis
performed were MRD negative at the 3-month follow-up visit -
Alle glemte i dag, at det ikke kun handler om OC, men om http://files.shareholder.com/downloads/AMDA-KPIBN/2774297033x0x689456/E648D1D6-1935-44B9-8017-69783BBE0402/2013_IWCLL_ofa_991_CLL_Offner_poster_FINAL.pdf
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Det er en forbavsende styrke GEN viser i dag. Mon vi har vendt faldet ryggen og går ind i en ny fase nu?
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Complement Activations through IgG Hexamers
Complement activation by antibodies represents a potent form of immune defense. By using cryo-electron tomography and mutagenesis studies we reveal the molecular mechanism by which antibody complexed to antigen triggers complement activation. Our data provide a model for understanding complement activation by antibodies and provides leads for its modulation.
Janine Schuurman, Ph.D., Director, Strategic Research, Genmab B.V., The Netherlands -
Muligvis gammelt nyt. Der er så meget pt...http://www.ibclifesciences.com/AntibodyEng/agenda.xml
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Carnegie har en rigtig god pointe omkring Genmab. med over 30+% af patienter med Gazyva der har grade 3´+ infusion eller neutropenia events vil en meget stor del af de patienter nok stoppe med Gazyva og gå Arzerra eller Rituxan
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Så selv hvis Gazyva bliver lægernes første valg, vil en stor af patienterne nok indse at de ikke kan tåle Gazyva og skifte behandling ?
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I patienter uden NOTCH1 mutation er PFS 23,3 for OC kombinationen https://ash.confex.com/ash/2013/webprogram/Paper58266.html
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