Genmab — Juni 2019
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Alle må kritiseres pænt og ordentligt
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@Vitus, Georgebest har altså ret, der findes ikke bedre end Bulder og Sukkeralf, super dygtige og saglige
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Hvis kommentarerne kunne holdes til at omhandle emnet og ikke skribenten, så ville vi være langt. Men nogle drømme må jo dø.
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Det tog 5 måneder for Pembrolizumab. Side 13. https://www.focr.org/sites/default/files/Friends Annual Meeting Panel 3 Slides.pdf
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jeg tænker, at der ingen grund er til panik. Fda ved jo også, at de har fremtidens SOC mellem hænderne. Så skal t’erne krydses og i’erne dottes til perfektion
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Lad os da håbe der ikke går 5 mdr for maia. For så lugter begynder det af nedjustering
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Genmab Announces U.S. FDA Approval of DARZALEX
(daratumumab) in Combination with Lenalidomide and Dexamethasone in Frontline Multiple Myeloma
Company AnnouncementDARZALEX (daratumumab) approved by U.S. FDA in combination with lenalidomide and dexamethasone for the treatment of adult patients with newly diagnosed multiple myeloma who are ineligible for autologous stem cell transplant
Approval based on Phase III MAIA study
Copenhagen, Denmark; June 27, 2019 – Genmab A/S (Nasdaq Copenhagen: GEN) -
offer their patients the option to add DARZALEX to this regimen in the U.S.,” said Jan van de Winkel, Ph.D., Chief Executive Officer of Genmab.
The approval was based on data from the Phase III MAIA (MMY3008) study of daratumumab in combination with lenalidomide and dexamethasone as treatment for patients with newly diagnosed multiple myeloma, who are not candidates for high dose chemotherapy and ASCT. Data from this study was presented as a Late-Breaking Abstract at the 2018 American Society o
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Dejligt!
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Fedt!
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Ikke noget hurlumhej med sc, men soc har også ret
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