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Genmab — December 2018

Planlagt Fastgjort Låst Flyttet Genmab
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Denne tråd er blevet slettet. Kun brugere med emne behandlings privilegier kan se den.
  • DarvinD Offline
    DarvinD Offline
    Darvin
    wrote on sidst redigeret af
    #576

    Hvis du kan din Starwars - ved du at de gode altid vinder til sidst 🙂

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    0
    • StockBullS Offline
      StockBullS Offline
      StockBull
      wrote on sidst redigeret af
      #577

      Der har vel ogsaa vaeret alternative behandlinger de andre gange hvor de har faaet fast track review

      1 Reply Last reply
      0
      • StockBullS Offline
        StockBullS Offline
        StockBull
        wrote on sidst redigeret af
        #578

        Kan ikke forestille mig en situation hvor MDR 24 giver slow track og MDR 30 giver fast track

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        0
        • Helge_LarsenPI-redaktørH Offline
          Helge_LarsenPI-redaktørH Offline
          Helge_LarsenPI-redaktør
          wrote on sidst redigeret af
          #579

          https://play.borsen.dk/social/5c074115595ab4f00a32b3ae

          1 Reply Last reply
          0
          • E Offline
            E Offline
            E_L
            wrote on sidst redigeret af
            #580

            Daratumumab and Selinexor presentation
            https://www.karyopharm.com/wp-content/uploads/2018/12/SDd-ASH2018-Final_2Dec18-1.pdf

            1 Reply Last reply
            0
            • K Offline
              K Offline
              kkjoel
              wrote on sidst redigeret af
              #581

              @Pensionisten, ..
              PI?

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              0
              • K Offline
                K Offline
                kkjoel
                wrote on sidst redigeret af
                #582

                Åh, javel 🙂

                1 Reply Last reply
                0
                • G Offline
                  G Offline
                  gentogen
                  wrote on sidst redigeret af
                  #583

                  Det afgørende for RTOR er, a tder er tale om sNDA/sBLA, der kan forbedre eksisterende behandling. Unmet need er ikke et krav.

                  1 Reply Last reply
                  0
                  • E Offline
                    E Offline
                    E_L
                    wrote on sidst redigeret af
                    #584

                    For ADCT-301, we now have the dosing data to support further investigation in a planned pivotal Phase II trial in patients with relapsed or refractory Hodgkin lymphoma, which we look forward to initiating in 2019.” from ADC Therapeutics website

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                    • E Offline
                      E Offline
                      E_L
                      wrote on sidst redigeret af
                      #585

                      also, further investigation of ADCT-301 in T-cell lymphoma

                      1 Reply Last reply
                      0
                      • E Offline
                        E Offline
                        E_L
                        wrote on sidst redigeret af
                        #586

                        ADCT presser pdf
                        https://adctherapeutics.com/downloads/1544013666.pdf

                        1 Reply Last reply
                        0
                        • B Offline
                          B Offline
                          bikube
                          wrote on sidst redigeret af
                          #587

                          NEXT og En Indgang går sammen under nyt navn - Det må da blive "Den næste Dør", som Osvald Helmuth sagde - "og det vil jeg sgu ikke".

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                          0
                          • BulderB Offline
                            BulderB Offline
                            Bulder
                            wrote on sidst redigeret af
                            #588

                            @ gentogen 13:43. Nej okay. Kan vi så omvendt konkludere, at hvis der ikke bevilges RTOR, så er det fordi FDA mener, at det ikke forbedrer eksisterende behandling?

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                            0
                            • BulderB Offline
                              BulderB Offline
                              Bulder
                              wrote on sidst redigeret af
                              #589

                              Ikke endnu. Men der var jo en, der fandt en lille overset note i en Gravesen-skrivelse forleden.

                              1 Reply Last reply
                              0
                              • BulderB Offline
                                BulderB Offline
                                Bulder
                                wrote on sidst redigeret af
                                #590

                                Hvis de ikke søger RTOR, så er det fordi de har fået et vink fra FDA om at det vil være forgæves. Winkel talte på CC om nye speedy procedurer hos FDA.

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                                0
                                • G Offline
                                  G Offline
                                  gentogen
                                  wrote on sidst redigeret af
                                  #591

                                  14:11. Nej. FDA har fire kriterier:
                                  • Drugs likely to demonstrate substantial improvements over available therapy,
                                  • Straight forward study designs, as determined by the review division and the OCE.
                                  • Endpoints that can be easily interpreted
                                  • Supplements with CMC formulation changes and supplements with pharmacology/toxicology data will be excluded.

                                  1 Reply Last reply
                                  0
                                  • BulderB Offline
                                    BulderB Offline
                                    Bulder
                                    wrote on sidst redigeret af
                                    #592

                                    De tre er uden problemer. Men så er der lige substantial improvements.

                                    1 Reply Last reply
                                    0
                                    • FantomasF Offline
                                      FantomasF Offline
                                      Fantomas
                                      wrote on sidst redigeret af
                                      #593

                                      A hva, har du ikke set tallene fra Maia studiet endnu? Hvis ikke det er et substantial improvement, så er det fordi du havde forventet en kur.

                                      1 Reply Last reply
                                      0
                                      • FantomasF Offline
                                        FantomasF Offline
                                        Fantomas
                                        wrote on sidst redigeret af
                                        #594

                                        Husk på, at selv om enkelte personer ikke ser lyset, så fik Maia center stage, oral abstract presentation efter Late breaking ansøgning.

                                        1 Reply Last reply
                                        0
                                        • FantomasF Offline
                                          FantomasF Offline
                                          Fantomas
                                          wrote on sidst redigeret af
                                          #595

                                          Selv Rajkumar anerkender jo også at Darzalex forbedre behandlingen, han anfægter jo kun om det er 135.000 USD per år bedre..

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                                          0

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