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Genmab — Maj 2021

Planlagt Fastgjort Låst Flyttet Genmab
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Denne tråd er blevet slettet. Kun brugere med emne behandlings privilegier kan se den.
  • BulderB Offline
    BulderB Offline
    Bulder
    wrote on sidst redigeret af
    #683

    In this case primary completion and completion is not changed, so they are probably not stopping the trial.

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    • S Offline
      S Offline
      Sukkeralf
      wrote on sidst redigeret af
      #684

      Andrew skriver SeaGen styrer dette studie, så ikke meget held der !

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      • S Offline
        S Offline
        Sukkeralf
        wrote on sidst redigeret af
        #685

        Andrew writes that it is SeaGen that runs this study - so no luck there

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        • S Offline
          S Offline
          Sukkeralf
          wrote on sidst redigeret af
          #686

          Such impressive deals on preclinical programs:

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          • S Offline
            S Offline
            Sukkeralf
            wrote on sidst redigeret af
            #687

            Just a moment...

            favicon

            (www.firstwordpharma.com)

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            • M Offline
              M Offline
              martinicph
              wrote on sidst redigeret af
              #688

              Man kunne skrive til, [email protected]. Måske de svarer lige så hurtigt som Andrew. 🙂

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              • troldmandenT Offline
                troldmandenT Offline
                troldmanden
                wrote on sidst redigeret af
                #689

                Når et studie standses så tidligt før tid så er det hvis mere reglen end undtagelsen det er dårligt nyt. Så vi skal ud i undtagelsen her hvis det er.... Der bør relativt hurtigt komme meddelelse med begrundelse

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                • D Offline
                  D Offline
                  deleted-user
                  wrote on sidst redigeret af
                  #690

                  Er studiet ikke forsat aktivt og rekruttering stoppet?

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                  • S Offline
                    S Offline
                    Sukkeralf
                    wrote on sidst redigeret af
                    #691

                    Jo - så helt galt er det ikke

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                    • BulderB Offline
                      BulderB Offline
                      Bulder
                      wrote on sidst redigeret af
                      #692

                      Hvis der var alvorlige AE ville de jo ikke fortsætte med at behandle dem, der er rekrutteret.

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                      • BulderB Offline
                        BulderB Offline
                        Bulder
                        wrote on sidst redigeret af
                        #693

                        Det er nok snarere på effektsiden at hunden ligger begravet.

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                        • S Offline
                          S Offline
                          Sukkeralf
                          wrote on sidst redigeret af
                          #694

                          Or maybe just at stop of recruitment until this have been decided:

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                          • S Offline
                            S Offline
                            Sukkeralf
                            wrote on sidst redigeret af
                            #695

                            The safety run-in period will evaluate the safety of a weekly schedule. The highest dose level that is considered safe will be the recommended phase 2 dose (RP2D) and will be used in Part A. In Part A, participants will be randomized in a 1:1 ratio to receive tisotumab vedotin intravenously (IV) every 3 weeks (Q3W regimen) or the safety run-in RP2D on Days 1, 8, and 15 of every 4-week cycle (weekly regimen; 3Q4W) if a RP2D has been identified. Participants who enroll in Part B will receive tisot

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                            • S Offline
                              S Offline
                              Sukkeralf
                              wrote on sidst redigeret af
                              #696

                              tumab vedotin intravenously (IV) every 3 weeks (Q3W regimen) or the safety run-in RP2D on Days 1, 8, and 15 of every 4-week cycle (weekly regimen; 3Q4W) if a RP2D has been identified. Participants who enroll in Part B will receive tisotumab vedotin on Days 1, 8, and 15 of every 4-week cycle (weekly regimen) at a pre-specified dose level, if the dose level is considered safe and tolerable in the safety run-in period.

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                              • E Offline
                                E Offline
                                E_L
                                wrote on sidst redigeret af
                                #697

                                that could also be possible, hadn't thought about that

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                                • E Offline
                                  E Offline
                                  E_L
                                  wrote on sidst redigeret af
                                  #698

                                  AbbVie routinely hiked prices for Humira, Imbruvica and abused patents to extend monopoly: congressional report https://www.fiercepharma.com/pharma/abbvie-repeatedly-raised-prices-for-humira-imbruvica-and-abused-u-s-patent-system-to-extend

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                                  • E Offline
                                    E Offline
                                    E_L
                                    wrote on sidst redigeret af
                                    #699

                                    I don't think we have to worry that epcoritamab will be sold too cheap with Abbvie as partner...

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                                    • D Offline
                                      D Offline
                                      deleted-user
                                      wrote on sidst redigeret af
                                      #700

                                      Lyttede til Andrew Carlsen på Investorevent fra Nordnet i dag. Bemærker, at han får sagt, at optionen omkring CD38 er en head to head sammenligning med Dara. Kunne man tænke sig, at man har indskrevet præcist hvilket resultat Genmab som minimum skal levere for hexa for, at optionen exercises for, at undgå JnJ spekulerer ensidig i egne økonomisk interesse?

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                                      • BulderB Offline
                                        BulderB Offline
                                        Bulder
                                        wrote on sidst redigeret af
                                        #701

                                        JnJ kan godt vælge at gå ind på basis af nuværende studie, men de kan også vente på et head to head studie. Og endvidere et dara i dlbcl - fandt vi ud af i går. Det kan næppe være beskrevet på forhånd, hvor tærskelen ligger. Det må være op til JnJ suverænt. Lige som med sgen i sin tid med tiso.

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                                        • D Offline
                                          D Offline
                                          deleted-user
                                          wrote on sidst redigeret af
                                          #702

                                          Er der ikke en markant forskel i og med hexa skal konkurrere med et eksisterende target? Anyways det var min tolkning af kommentaren fra Andres C. sammenholdt med JnJ eventuelt modsatrettede interesser omkring et bedre produkt og økommisk tab/gevinst. Normalt vil en option være baseret på en X-værdi der er målbar og ikke blot et tjatjooo måskeeee vurdering af den ene part.

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