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Genmab — Februar 2013

Planlagt Fastgjort Låst Flyttet Genmab
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Denne tråd er blevet slettet. Kun brugere med emne behandlings privilegier kan se den.
  • D Offline
    D Offline
    deleted-user
    wrote on sidst redigeret af
    #105

    316K

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    • SolsenS Offline
      SolsenS Offline
      Solsen
      wrote on sidst redigeret af
      #106

      http://www.bloomberg.com/news/2013-02-15/genmab-rises-as-danske-sees-fda-breakthrough-copenhagen-mover.html?cmpid=yhoo Måske allerede posted

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      • D Offline
        D Offline
        deleted-user
        wrote on sidst redigeret af
        #107

        det er merill lynch, credit suisse på den ene side og ens og ddb på den anden side. Jeg tror det må være ATP der losser ud

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        • G Offline
          G Offline
          gentogen
          wrote on sidst redigeret af
          #108

          Vedr. Solsens link. Så kan Ofa måske profitere af Ibrutinib. In combination with ofatumumab (Arzerra) on patients with chronic lymphocytic leukemia / small lymphocytic leukemia / prolymphocytic leukemia1 (CLL/SLL/ PLL1) and Richter transformation, results demonstrate that the combination was well-tolerated and highly active in patients with heavily pretreated relapsed/refractory CLL/SLL. The drug is described to have a rapid onset of response, low relapse rate, and favorable safety profile.http

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          • G Offline
            G Offline
            gentogen
            wrote on sidst redigeret af
            #109

            http://www.prohostbiotech.com/_blog/News_and_Comments/post/PHARMACYCLICS_IBRUTINIB,_THE_NEXT_RITUXAN_AND_MORE_/

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            • G Offline
              G Offline
              gentogen
              wrote on sidst redigeret af
              #110

              eller det modsatte http://clinicaltrials.gov/ct2/show/NCT01578707?term=ofatumumab&phase=2&rank=11

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              • G Offline
                G Offline
                gentogen
                wrote on sidst redigeret af
                #111

                In this ongoing trial patients with relapsed/refractory CLL/SLL who have received two or more prior therapies are treated with ibrutinib (420 mg) daily until disease progression, followed by concomitant ofatumumab with continued ibrutinib until progression.

                For the CLL/SLL/PLL patients the overall response rate, as measured by IWCLL criteria and progression-free survival is 100%, with a median follow-up of 9.8 months

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                • D Offline
                  D Offline
                  deleted-user
                  wrote on sidst redigeret af
                  #112

                  Så de laver head to head med ofa i den indikation den er godkendt i. Det er svært at se fordelen i for Genmab.

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                  • S Offline
                    S Offline
                    Sukkeralf
                    wrote on sidst redigeret af
                    #113

                    Ibrutinib bliver en stor spiller og også her har Janssen været vågne og villige til at betale for en god aftale. Lad os håbe at Daratumumab bliver en lige så stor succes - og ikke helt uvæsentligt, at Janssen sidder på både Ibrutinib og Daratumumab. Hvem ved det kan blive fremtidens killer-kombi uden kemo !

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                    • S Offline
                      S Offline
                      Sukkeralf
                      wrote on sidst redigeret af
                      #114

                      Jan har tidligere nævnt, at de håbede på at GSK/Janssen ville starte fase III kombi med Ibrutinib og Ofatumumab i 2013. Det må vi se om sker !!

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                      • S Offline
                        S Offline
                        Sukkeralf
                        wrote on sidst redigeret af
                        #115

                        Det tegner i hvert fald lovende for patienter, at man i fremtiden har nogle ekstremt lovende kombinationsbehandlinger uden kemo 🙂

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                        • S Offline
                          S Offline
                          Sukkeralf
                          wrote on sidst redigeret af
                          #116

                          http://ir.pharmacyclics.com//ReleaseDetail.cfm?ReleaseID=739863

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                          • investor1989I Offline
                            investor1989I Offline
                            investor1989
                            wrote on sidst redigeret af
                            #117

                            Det er altså meget spændende at de gør dette med ibrutinib

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                            • investor1989I Offline
                              investor1989I Offline
                              investor1989
                              wrote on sidst redigeret af
                              #118

                              Især når man så tænker på at man har ændret protokol i phase I/II studiet efter Janssen kom ombord....

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                              • S Offline
                                S Offline
                                Sukkeralf
                                wrote on sidst redigeret af
                                #119

                                Ja og det er jo lidt de samme cancer indikationer daratumumab og Ibrutinib går efter, så hvis der er additiv effekt eller endnu bedre synergier, så sidder de på to hotte stoffer i kombinationer - det kan da ikke andet end blive stort !

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                                • investor1989I Offline
                                  investor1989I Offline
                                  investor1989
                                  wrote on sidst redigeret af
                                  #120

                                  måske man skulle købe lidt J&J aktier til pensionen

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                                  • investor1989I Offline
                                    investor1989I Offline
                                    investor1989
                                    wrote on sidst redigeret af
                                    #121

                                    den er ikke voldsom dyr

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                                    • investor1989I Offline
                                      investor1989I Offline
                                      investor1989
                                      wrote on sidst redigeret af
                                      #122

                                      Det ville give et kæmpe boost til genmabs markedsværdi at dara NDA kan indsendes når phase I/II studiet er færdigt

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                                      • D Offline
                                        D Offline
                                        deleted-user
                                        wrote on sidst redigeret af
                                        #123

                                        ja det vil helt sikkert gøre casen helt anderledes i og med at man så vil få en "rituxian agtig" status i MM.

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                                        0
                                        • D Offline
                                          D Offline
                                          deleted-user
                                          wrote on sidst redigeret af
                                          #124

                                          men man tør jo næsten ikke tro på det

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