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Genmab — Juni 2017

Planlagt Fastgjort Låst Flyttet Genmab
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  • J Offline
    J Offline
    Jedi
    wrote on sidst redigeret af
    #649

    det vil jo være fint 🙂

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    • F Offline
      F Offline
      flottenschmecker
      wrote on sidst redigeret af
      #650

      Det er lige det - kunne det ikke tyde på, at man også går efter godkendelse af dara ifm ASCT

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      • F Offline
        F Offline
        flottenschmecker
        wrote on sidst redigeret af
        #651

        umiddelbart kunne man vel "bare" teste maintenance effekten

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        • D Offline
          D Offline
          dohk
          wrote on sidst redigeret af
          #652

          Kan se at Cassiopeia kun rekruterer i Frankring, Belgien og Holland...Så kan de overhovedet få en FDA approval på det studie?

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          • D Offline
            D Offline
            dohk
            wrote on sidst redigeret af
            #653

            Det er jo et sponsoreret studie, så måske også derfor at Janssen og Genmab ved mindre om hvordan rekrutteringen går.

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            • J Offline
              J Offline
              Jedi
              wrote on sidst redigeret af
              #654

              Jeg ved ikke om det er muligt at få en godkendelse allerede ifm ASCT og første fase? - det ene primære mål evalueres efter første fase, men det andet er PFS efter anden fase. Jeg ved ikke om der kan godkendes uden at PFS målet er evalueret

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              • BulderB Offline
                BulderB Offline
                Bulder
                wrote on sidst redigeret af
                #655

                Kunne forestille mig at Cassiopeia var "beregnet" for Europa. I US kommer det snarere til at hedde D+KRd.

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                • E Offline
                  E Offline
                  E_L
                  wrote on sidst redigeret af
                  #656

                  I could really appreciate some Friday after-close good news today, just to piss off the dumbass that has been selling whole week

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                  • F Offline
                    F Offline
                    flottenschmecker
                    wrote on sidst redigeret af
                    #657

                    haha - you could hope for the FDA

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                    • BulderB Offline
                      BulderB Offline
                      Bulder
                      wrote on sidst redigeret af
                      #658

                      Kommer til at tænke på, at PFS-målet nok kommer til at spille en mindre rolle i fremtidige studier, da man efterhånden er i stand til at give et hurtigt billede af effekten ved at måle MRDneg i stedet. Skulle kunne betyde hurtigere studie-resultater.

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                      • B Offline
                        B Offline
                        bibob
                        wrote on sidst redigeret af
                        #659

                        Ja, det ville være godt at kappe måske et 1/2 år af et studie når man nu kender virke mekanismen.

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                        • F Offline
                          F Offline
                          flottenschmecker
                          wrote on sidst redigeret af
                          #660

                          ifht maintenance slipper vi nok ikke for pfs tallene...

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                          • G Offline
                            G Offline
                            gentogen
                            wrote on sidst redigeret af
                            #661

                            https://myelomaresearchnews.com/2016/09/21/minimal-residual-disease-in-myeloma-suggested-as-clinical-trial-endpoint-but-experts-disagree/

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                            • BulderB Offline
                              BulderB Offline
                              Bulder
                              wrote on sidst redigeret af
                              #662

                              FDA kommer til at gi' sig på et tidspunkt https://www.myelomacrowd.org/minimal-residual-disease-negativity-becomes-new-end-point-myeloma-therapy/

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                              • B Offline
                                B Offline
                                bibob
                                wrote on sidst redigeret af
                                #663

                                Det er sikkert Bulder. De kan ikke komme uden om Dara. 🙂

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                                • E Offline
                                  E Offline
                                  E_L
                                  wrote on sidst redigeret af
                                  #664

                                  Not sure it this NCT was posted here already, Janssen mo
                                  ves fast - NCT03177460 A Pilot Presurgical Study of Daratumumab in Men With High-Risk Localized Prostate Cancer - https://clinicaltrials.gov/ct2/show/NCT03177460?term=daratumumab+OR+ofatumumab&lup_s=06%2F08%2F2017&rank=1

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                                  • J Offline
                                    J Offline
                                    JKY_VH
                                    wrote on sidst redigeret af
                                    #665

                                    jo den mener jeg vi har set

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                                    • BulderB Offline
                                      BulderB Offline
                                      Bulder
                                      wrote on sidst redigeret af
                                      #666

                                      Her er interviewet med Moreau om Cassiopeia. Han siger at de lukker Q1 2017 og data i 2018. https://www.youtube.com/watch?v=wttCv152AK4&t=19s

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                                      • G Offline
                                        G Offline
                                        GeorgeBest
                                        wrote on sidst redigeret af
                                        #667

                                        EL - why would MD Andersson do this prostate cancer study as monotherapy? Wouldn't it be better to combine dara with an approved prostate cancer drug like Xtandi?

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                                        • E Offline
                                          E Offline
                                          E_L
                                          wrote on sidst redigeret af
                                          #668

                                          I am not sure, but this is on patients that are already scheduled to have prostatectomy -my guess is that they are just trying to get extra information out of that patient group?

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