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  4. Genmab — Februar 2024

Genmab — Februar 2024

Planlagt Fastgjort Låst Flyttet Genmab
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  • BulderB Offline
    BulderB Offline
    Bulder
    wrote on sidst redigeret af
    #220

    En vis konkurrence - i 2. linje. 1/3 får grad 3 eller værre problemer med synet.

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    0
    • Helge_LarsenPI-redaktørH Offline
      Helge_LarsenPI-redaktørH Offline
      Helge_LarsenPI-redaktør
      wrote on sidst redigeret af
      #221

      Godmorgen 🙂

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      0
      • P Offline
        P Offline
        Plimsoller
        wrote on sidst redigeret af
        #222

        God morgen 🙂

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        • S Offline
          S Offline
          Stroka
          wrote on sidst redigeret af
          #223

          God morgen 🙂

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          0
          • L Offline
            L Offline
            LP90
            wrote on sidst redigeret af
            #224

            God morgen 🙂

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            • E Offline
              E Offline
              E_L
              wrote on sidst redigeret af
              #225

              AMGEN: TEPEZZA® (teprotumumab-trbw) generated $448 million of sales for the period. TEPEZZA is the first and only FDA-approved treatment for thyroid eye disease (TED). -Sales figures reflect only sales in the period from Oct. 6 2023 through the end of the year, and not the full quarter. https://investors.amgen.com/news-releases/news-release-details/amgen-reports-fourth-quarter-and-full-year-2023-financial

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              • E Offline
                E Offline
                E_L
                wrote on sidst redigeret af
                #226

                In December 2023, TEPEZZA received orphan drug designation in Japan for patients with moderate to severe active thyroid eye disease (TED).
                A New Drug Application was submitted for TEPEZZA in Japan based on the results from the OPTIC-J study evaluating TEPEZZA in patients with active TED.
                A Phase 3 study of TEPEZZA in Japan for chronic or low clinical activity score (CAS) TED continues to enroll patients.

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                • E Offline
                  E Offline
                  E_L
                  wrote on sidst redigeret af
                  #227

                  The Company plans to initiate a Phase 3 study evaluating the subcutaneous route of administration of TEPEZZA in patients with TED in H1 2024.

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                  • S Offline
                    S Offline
                    Sukkeralf
                    wrote on sidst redigeret af
                    #228

                    UUHFFF - now we hate these sc versions 😞

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                    • S Offline
                      S Offline
                      Sukkeralf
                      wrote on sidst redigeret af
                      #229

                      But Amgen seems to being doing a good job - thats so good 🙂

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                      • S Offline
                        S Offline
                        Sukkeralf
                        wrote on sidst redigeret af
                        #230

                        Lundbeck igangsætter
                        fase 3-studie med Lu AF82422.

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                        • S Offline
                          S Offline
                          Sukkeralf
                          wrote on sidst redigeret af
                          #231

                          Link Preview Image
                          Lundbeck igangsætter fase 3-studie med CNS-kandidat

                          På trods af de umiddelbart ufordelagtige statistiske resultater fra et tidligere studie igangsætter Lundbeck nu et fase 3-studie med Lu AF82422.

                          favicon

                          (medwatch.dk)

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                          • E Offline
                            E Offline
                            E_L
                            wrote on sidst redigeret af
                            #232

                            we'll see how that works out for Tepezza SC, we don't know if the contracts are similar, but at at least Genmab now knows how to proceed with a potential arbitrage 😄 The news in itself is not real news in that Horizon was looking at SC already in 2020 with Halozyme, but i imagine Xeris Biopharma will run with the deal after this
                            https://finance.yahoo.com/news/xeris-xers-licensing-deal-amgen-133000124.html

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                            • G Offline
                              G Offline
                              gentogen
                              wrote on sidst redigeret af
                              #233

                              Når nu SC-versionerne juridisk set er helt nye produkter, kan Genmab så ikke bare selv lave dem?

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                              • E Offline
                                E Offline
                                E_L
                                wrote on sidst redigeret af
                                #234

                                the Ph3 EPCORE FL-2 trials started recruiting https://classic.clinicaltrials.gov/ct2/history/NCT06191744?B=3&A=2&C=merged#StudyPageTop

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                                • JørgenVarnæsJ Offline
                                  JørgenVarnæsJ Offline
                                  JørgenVarnæs
                                  wrote on sidst redigeret af
                                  #235

                                  Nice - full steam ahead. Any ideas as to how easy/difficult recruitment will be?

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                                  • JørgenVarnæsJ Offline
                                    JørgenVarnæsJ Offline
                                    JørgenVarnæs
                                    wrote on sidst redigeret af
                                    #236

                                    incidence US = 15k/year

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                                    • E Offline
                                      E Offline
                                      E_L
                                      wrote on sidst redigeret af
                                      #237

                                      i expect fast recruitment really; epco trials have done well, even during covid. Results for FL with epco are very very good, so i would think any doctor that can get his patient into this regimen for free via a trial
                                      will try...

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                                      • E Offline
                                        E Offline
                                        E_L
                                        wrote on sidst redigeret af
                                        #238

                                        @gentogen some antibodies may not need an addition to be admistered SC and then genmab can do it itself, depends also on how potent the drug is and how much you will need to dose (like epco, and possibly HexaCD38). But for others i think outside technology will be used, i mean large pharmas also do that

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                                        • JørgenVarnæsJ Offline
                                          JørgenVarnæsJ Offline
                                          JørgenVarnæs
                                          wrote on sidst redigeret af
                                          #239

                                          Primary outcome measured as % of CRs at 30 months. Will take some time before we get there

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