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Genmab — Maj 2018

Planlagt Fastgjort Låst Flyttet Genmab
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Denne tråd er blevet slettet. Kun brugere med emne behandlings privilegier kan se den.
  • P Offline
    P Offline
    Plimsoller
    wrote on sidst redigeret af
    #81

    God morgen 🙂

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    • P Offline
      P Offline
      polle1
      wrote on sidst redigeret af
      #82

      God morgen 🙂

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      • J Offline
        J Offline
        JohnW
        wrote on sidst redigeret af
        #83

        Ser I mulighed for noget kurspåvirkende nyt fra regnskabet d. 8.?

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        • R Offline
          R Offline
          Repsac
          wrote on sidst redigeret af
          #84

          En opjustering vil være kurspåvirkende.

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          • O Offline
            O Offline
            OHW
            wrote on sidst redigeret af
            #85

            Den vil i givet fald allerede være indregnet i kursen 😉 Der vil komme noget fra regnskabet, som short fondene ikke kan håndtere. Der skal hard core nyheder til for at ændre fastlåsningen, eller?

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            • O Offline
              O Offline
              OHW
              wrote on sidst redigeret af
              #86

              ..ikke..

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              • Legolas23L Offline
                Legolas23L Offline
                Legolas23
                wrote on sidst redigeret af
                #87

                Opjustering sker ikke før der kommer en 1. linie godkendelse. Måske en opjustering og kurspåvirkende nyheder i Q3, hvis der kommer gode data på data i solide.

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                • J Offline
                  J Offline
                  JohnW
                  wrote on sidst redigeret af
                  #88

                  Skulle Alcyone godkendelsen i EU ikke komme i denne måned?

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                  • Legolas23L Offline
                    Legolas23L Offline
                    Legolas23
                    wrote on sidst redigeret af
                    #89

                    D. 21 maj, men der skal være sikkerhed for vi rammer inden for salgsguidiance.

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                    • BulderB Offline
                      BulderB Offline
                      Bulder
                      wrote on sidst redigeret af
                      #90

                      Det er US, der har dato senest 21. maj. CHMP- (EU) anbefalingen er ikke kommet endnu. Når den kommer går der 60 dage til den endelige afgørelse. Genmab venter endelig afgørelse i august.

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                      • M Offline
                        M Offline
                        Mayflower
                        wrote on sidst redigeret af
                        #91

                        Noget positivt om TV eller ofa vil være rigtig godt. No one likes a one-trick pony. 🙂

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                        • S Offline
                          S Offline
                          Sukkeralf
                          wrote on sidst redigeret af
                          #92

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                          • P Offline
                            P Offline
                            Plimsoller
                            wrote on sidst redigeret af
                            #93

                            Alcyone er primært for EU såvidt jeg kan forstå, men hvad er så primært for USA, og hvor er vi med det?

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                            • S Offline
                              S Offline
                              Sukkeralf
                              wrote on sidst redigeret af
                              #94

                              Dara-Rev-Dex - fase III kommer i sensommeren, så filing omkring årsskiftet og godkendelse sommer 2019

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                              • E Offline
                                E Offline
                                E_L
                                wrote on sidst redigeret af
                                #95

                                @Sukkeralf I cant figure out what drug Spicer is talking about; is it HuMax-AXL-ADC?

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                                • E Offline
                                  E Offline
                                  E_L
                                  wrote on sidst redigeret af
                                  #96

                                  coincidentally this HuMax-AXL-ADC Safety Study in Patients With Solid Tumors is now looking to recruit almost 300 patients, alsmost 2x what they said first https://clinicaltrials.gov/ct2/history/NCT02988817?A=5&B=6&C=merged

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                                  • E Offline
                                    E Offline
                                    E_L
                                    wrote on sidst redigeret af
                                    #97

                                    also: "The Expansion part of the trial has been initiated " ; i read that as :
                                    they started phase 2 ?

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                                    • S Offline
                                      S Offline
                                      Sukkeralf
                                      wrote on sidst redigeret af
                                      #98

                                      I think he mentioned AXL molecules (probably Bemcentinib) in combination with Pemblizumab (Keytruda) and Erlotinib (Tarceva). BergenBio´s Bemcentinib is in clinical studies with both.

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                                      • S Offline
                                        S Offline
                                        Sukkeralf
                                        wrote on sidst redigeret af
                                        #99

                                        Just a link to show that AXL becomes more and more intresting

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                                        • E Offline
                                          E Offline
                                          E_L
                                          wrote on sidst redigeret af
                                          #100

                                          ok thx

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