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  4. Genmab — August 2024

Genmab — August 2024

Planlagt Fastgjort Låst Flyttet Genmab
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  • E Offline
    E Offline
    E_L
    wrote on sidst redigeret af
    #108

    I like seeing these small new epco trials instigated by hospitals/ University centers/ MD's , they indicate interest from the field to work with epco

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    • Helge_LarsenPI-redaktørH Offline
      Helge_LarsenPI-redaktørH Offline
      Helge_LarsenPI-redaktør
      wrote on sidst redigeret af
      #109

      Godmorgen 🙂

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      • S Offline
        S Offline
        Stroka
        wrote on sidst redigeret af
        #110

        God morgen 🙂

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        • B Offline
          B Offline
          bibob
          wrote on sidst redigeret af
          #111

          God morgen. 🙂

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          • L Offline
            L Offline
            LP90
            wrote on sidst redigeret af
            #112

            Godmorgen 🙂

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            • E Offline
              E Offline
              E_L
              wrote on sidst redigeret af
              #113

              Aug. 6, 2024,
              Ram Selvaraju, H.C. Wainwright, reiterated the Buy rating on Genmab. The price target remains the same with $50.00. "Despite BioNTech’s decision to step back from the co-development of acasunlimab, Selvaraju’s confidence in the drug remains unshaken, as he finds the clinical results presented at ASCO 2024 to be highly encouraging." https://markets.businessinsider.com/news/stocks/buy-rating-affirmed-for-genmab-strong-clinical-results-and-solid-financial-valuation-1033645523

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              • E Offline
                E Offline
                E_L
                wrote on sidst redigeret af
                #114

                TEPEZZA® (teprotumumab-trbw) generated $479 million of sales in the second quarter. AMGEN REPORTS SECOND QUARTER 2024 https://investors.amgen.com/news-releases/news-release-details/amgen-reports-second-quarter-2024-financial-results

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                • E Offline
                  E Offline
                  E_L
                  wrote on sidst redigeret af
                  #115

                  Regulatory review of the New Drug Application (NDA) for TEPEZZA in Japan and multiple additional geographies continues.
                  A Phase 3 study of TEPEZZA in Japan continues to enroll patients with chronic or low clinical activity score TED.
                  A Phase 3 study evaluating the subcutaneous route of administration of TEPEZZA is enrolling patients with TED.

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                  • J Offline
                    J Offline
                    JKY_VH
                    wrote on sidst redigeret af
                    #116

                    Tak E L

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                    • E Offline
                      E Offline
                      E_L
                      wrote on sidst redigeret af
                      #117

                      Today, Exelixis announced it will discontinue the development of XB002, the company’s tissue factor (TF)-targeting ADC, as part of its portfolio prioritization efforts. Based on available data, the compound is unlikely to improve upon tisotumab vedotin or other competitor TF-targeting ADCs currently in development. https://ir.exelixis.com/news-releases/news-release-details/exelixis-announces-second-quarter-2024-financial-results-and

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                      • L Offline
                        L Offline
                        lahn1
                        wrote on sidst redigeret af
                        #118

                        Tak for nyhederne EL

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                        • E Offline
                          E Offline
                          E_L
                          wrote on sidst redigeret af
                          #119

                          i am sure there will be some Novo watchers here that can look our for any mim8 news today?

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                          • G Offline
                            G Offline
                            gentogen
                            wrote on sidst redigeret af
                            #120

                            Following regulatory interactions, Novo Nordisk now expects to submit Mim8 for the first regulatory approval during the first half of 2025.

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                            • R Offline
                              R Offline
                              Raun
                              wrote on sidst redigeret af
                              #121

                              Burde Genmab aktien egentlig ikke have steget, ovenpå udmeldingen at Biontech trak sig fra Gen1046?.... Er klar over at det selvfølgelig giver usikkerhed, når en partner trækker sig for et stof .Men at Genmab ikke går ud og søger ny aftale, eller selv overvejer at trække stikket fortæller jo også en hel del. - Tværtimod vælger Genmab selv at stå for udgifterne på et dyrt fase 3 forsøg. Hvilket må tolkes til at Genmab tror selv meget på stoffet, - og så må det jo egentlig være en gave at stå med

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                              • R Offline
                                R Offline
                                Raun
                                wrote on sidst redigeret af
                                #122

                                et stort set 100% eget stof, så tæt på mål?

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                                • R Offline
                                  R Offline
                                  Raun
                                  wrote on sidst redigeret af
                                  #123

                                  Der vil være noglee royalties til Biontech, hvis stoffet kom på markedet..... Men det kan da vel max være 10%

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                                  • BulderB Offline
                                    BulderB Offline
                                    Bulder
                                    wrote on sidst redigeret af
                                    #124

                                    The program will be subject to payment of certain milestones and a tiered single-digit royalty on net sales by Genmab to BioNTech.

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                                    • G Offline
                                      G Offline
                                      gentogen
                                      wrote on sidst redigeret af
                                      #125

                                      På sin vis enig. Genmab skulle jo alligevel have afholdt 50% af fase 3, så merudgiften er begrænset set i forhold til potentielle gevinst.

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                                      • G Offline
                                        G Offline
                                        gentogen
                                        wrote on sidst redigeret af
                                        #126

                                        Så der nået frem til fase 3 til halv pris. Det er da meget smart...

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                                        • BulderB Offline
                                          BulderB Offline
                                          Bulder
                                          wrote on sidst redigeret af
                                          #127

                                          Når genmab overtager det fulde ansvar, så er der i hvert fald for nuværende ikke noget i vejen med stoffet. Biontec trak sig fordi de skulle spare. Det bliver sikkert drøftet nærmere på CC.

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