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Genmab — April 2019

Planlagt Fastgjort Låst Flyttet Genmab
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Denne tråd er blevet slettet. Kun brugere med emne behandlings privilegier kan se den.
  • E Offline
    E Offline
    E_L
    wrote on sidst redigeret af
    #1151

    @Bulder yes, that shows good faith

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    • J Offline
      J Offline
      JKY_VH
      wrote on sidst redigeret af
      #1152

      Tak E L

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      • E Offline
        E Offline
        E_L
        wrote on sidst redigeret af
        #1153

        @Sukkeralf did you see BMS say anything about Humax IL8 in their earnings?

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        • S Offline
          S Offline
          Sukkeralf
          wrote on sidst redigeret af
          #1154

          I havent looked but would guess not

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          • B Offline
            B Offline
            bibob
            wrote on sidst redigeret af
            #1155

            God formiddag fra 10 km højde på vej sydpå. :-). Jeg kan se Genmab også lettede på vej nordpå. :-).

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            • E Offline
              E Offline
              E_L
              wrote on sidst redigeret af
              #1156

              ok, just because you came with the links just after their earnings

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              • E Offline
                E Offline
                E_L
                wrote on sidst redigeret af
                #1157

                Dr. Durie on Dara SC in the middle of the video
                (again nothing we don't know...) https://www.youtube.com/watch?v=a8_MB7o0MZo

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                • S Offline
                  S Offline
                  Sukkeralf
                  wrote on sidst redigeret af
                  #1158

                  Bulder RTOR ?

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                  • S Offline
                    S Offline
                    Sukkeralf
                    wrote on sidst redigeret af
                    #1159

                    From SG transcript: GSK has some fantastic data in multiple myeloma with the BCMA antibody drug conjugate. And what we hear from them is they're planning to submit in the second half of this year. And we're delighted through the impact in multiple myeloma. That is a potential large market. And they also are doing many other trials, including frontline. And so, that potentially could be a really big drug for GSK and really beneficial to patients and to Seattle genetics.

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                    • SolsenS Offline
                      SolsenS Offline
                      Solsen
                      wrote on sidst redigeret af
                      #1160

                      Hvis GK er lige så dygtige til at arbejde med BCMA stoffet sim Ofatumumab er der intet at frygte.

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                      • S Offline
                        S Offline
                        Sukkeralf
                        wrote on sidst redigeret af
                        #1161

                        favicon

                        (clinicaltrials.gov)

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                        • S Offline
                          S Offline
                          Sukkeralf
                          wrote on sidst redigeret af
                          #1162

                          Indtil videre i de lidt senere linier, men desværre ingen kombi med Dara

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                          0
                          • SolsenS Offline
                            SolsenS Offline
                            Solsen
                            wrote on sidst redigeret af
                            #1163

                            Gætter vi på MAIA approval i dag ?

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                            • S Offline
                              S Offline
                              Sukkeralf
                              wrote on sidst redigeret af
                              #1164

                              ja eller over weekenden

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                              • BulderB Offline
                                BulderB Offline
                                Bulder
                                wrote on sidst redigeret af
                                #1165

                                Sukkeralf: PR kræver ikke noget særligt studiedesign. Man indsender hele møllen på een gang. Når de omtaler et særligt design, antager jeg at det er motiveret i RTOR. Hvad ellers?

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                                • BulderB Offline
                                  BulderB Offline
                                  Bulder
                                  wrote on sidst redigeret af
                                  #1166

                                  FDA's accelerated approval mechanism

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                                  • S Offline
                                    S Offline
                                    Sukkeralf
                                    wrote on sidst redigeret af
                                    #1167

                                    Man kan ikke få RTOR på et endnu ikke godkendt stof

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                                    • S Offline
                                      S Offline
                                      Sukkeralf
                                      wrote on sidst redigeret af
                                      #1168

                                      Tænker at det måske har noget at gøre med at det jo i princippet blot er et fase II studie, men designet så man kan lave en ansøgning såfremt data er tilstrækkelig gode

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                                      • S Offline
                                        S Offline
                                        Sukkeralf
                                        wrote on sidst redigeret af
                                        #1169

                                        Ville være rart med en enkelt eller to gode nyheder før regnskab, så der kunne spørges ind til dette på CC og PI Q&A - fredags nyhed......fredags nyhed..........fredags nyhed

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                                        • BulderB Offline
                                          BulderB Offline
                                          Bulder
                                          wrote on sidst redigeret af
                                          #1170

                                          While RTOR currently is being piloted for only the most straightforward supplemental applications, future expansion to more complex supplements or to NEW molecular entities (NME). Måske det, de har i tankerne med accellerated https://www.focr.org/news/pink-sheet-real-time-oncology-review-has-sponsors-rethinking-what-data-share-us-fda-and-when

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