Genmab — Oktober 2017
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@Sukkeralf 10.22 Er interimdata ikke event drevet? - og dermed kan de komme før eller senere alt efter hvor mange events der indtræffer hvornår
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Jeg tænker også på at man mere og mere går over til at måle respons på MRD i stedet for PFS, som jo har den ulempe, at man skal vente i mange mdr for at få et pålideligt tal, hvorimod MRD kan måles langt tidligere. Fra sidste IMWG-summit: All discussants agreed that MRD testing can become the official measure of treatment response in myeloma clinical trials. https://www.myeloma.org/article/report-2017-summit-international-myeloma-working-group
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Kræftmidler forlænger ikke livet i syv ud af ti tilfælde
Hovedparten af de kræftmidler, der i perioden 2009-2013 blev godkendt af Det Europæiske Lægemiddelagentur, EMA, øger ikke overlevelsen eller livskvaliteten, viser ny britisk forskning. Men resultaterne bygger på en helt forkert præmis og er derfor irrelevante, mener Lægemiddelstyrelsen.
(medwatch.dk)
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Vi har vist kun hvad Rachel Gravesen skrev 25/8: The IDMC have yet to take the formal decision on what to do regarding the control group patients and whether they should be offered daratumumab. I would expect this to be something that is considered very soon and a decision taken and verified through the necessary channels ....
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those looking for a timeline; this was from Danske from the summer - https://www.andelskassen.dk/media/3616/genmab.pdf
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I think they were
refering to the data we saw Aug 24 http://ir.genmab.com/releasedetail.cfm?ReleaseID=1038151
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