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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.
  • 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

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        • 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

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                  0
                  • E Offline
                    E Offline
                    E_L
                    wrote on sidst redigeret af
                    #586

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

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                    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".

                      1 Reply Last reply
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                      • 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?

                        1 Reply Last reply
                        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.

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                              0
                              • BulderB Offline
                                BulderB Offline
                                Bulder
                                wrote on sidst redigeret af
                                #592

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

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                                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
                                      • B Offline
                                        B Offline
                                        bibob
                                        wrote on sidst redigeret af
                                        #596

                                        Mon ikke snart den handelskrig får en ende. Tror 2019 bliver et fint aktieår når mudderkastningen fra Trump og Xi ophører. Det ender vel med at de kindkysser. https://www.euroinvestor.dk/nyheder/2018/12/05/kina-er-sikker-paa-aftale-med-usa-i-loebet-af-toldpause-paa-90-dage/13940201

                                        1 Reply Last reply
                                        0
                                        • J Offline
                                          J Offline
                                          JKY_VH
                                          wrote on sidst redigeret af
                                          #597

                                          ja, lad os håbe at det snart får en ende.

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                                          0

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