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Genmab — November 2018

Planlagt Fastgjort Låst Flyttet Genmab
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Denne tråd er blevet slettet. Kun brugere med emne behandlings privilegier kan se den.
  • G Offline
    G Offline
    gentogen
    wrote on sidst redigeret af
    #721

    ClinicalTrials.gov

    favicon

    (clinicaltrials.gov)

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    • Helge_LarsenPI-redaktørH Offline
      Helge_LarsenPI-redaktørH Offline
      Helge_LarsenPI-redaktør
      wrote on sidst redigeret af
      #722

      God morgen. 🙂

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      • B Offline
        B Offline
        bibob
        wrote on sidst redigeret af
        #723

        God morgen. 🙂

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        • E Offline
          E Offline
          E_L
          wrote on sidst redigeret af
          #724

          God morgen. this Dara/Atezo NSCLC trial keeps intruiging me (probably in vain lol ), but why do you recruit 100 patients in a trial that does not work… https://clinicaltrials.gov/ct2/history/NCT03023423?A=22&B=23&C=merged

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          • E Offline
            E Offline
            E_L
            wrote on sidst redigeret af
            #725

            @bibob ; changing from IV to SC in the middle of a trial would mess up the (safety)data, no?

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            • laerlingenL Offline
              laerlingenL Offline
              laerlingen
              wrote on sidst redigeret af
              #726

              Hvis studiet er startet får man ikke lov til at ændre i protokollen

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              • BulderB Offline
                BulderB Offline
                Bulder
                wrote on sidst redigeret af
                #727

                I suppose the study goes on to find out what went wrong.

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                • B Offline
                  B Offline
                  bibob
                  wrote on sidst redigeret af
                  #728

                  @E L. and laerlingen. Ok, then they have to start a new trial, but they know the safety. ? could the new trial then be approved faster maybee.??

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                  • BulderB Offline
                    BulderB Offline
                    Bulder
                    wrote on sidst redigeret af
                    #729

                    Det er set før, at man har ændret i protokollen efter start. Men en så gennemgribende som administrationsmåden gør man næppe. I øvrigt er det jo et ISS-studie - og ikke Janssen - som går ud på at finde ud af hvordan dara og Venetoclax spiller sammen og ikke om sc er bedre end iv. Førtst i det øjeblik at sc er blevet standard vil man bruge det - vil jeg tro.

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                    • BulderB Offline
                      BulderB Offline
                      Bulder
                      wrote on sidst redigeret af
                      #730

                      Det er kun et fase 1-2 og et evt. senere fase 3 godkendelsesstudie vil sagtens kunne gå over til sc.

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                      • nohopeN Offline
                        nohopeN Offline
                        nohope
                        wrote on sidst redigeret af
                        #731

                        Hvis man skal være bagklog, hvilket er en af mine spidskompetencer, så kunne man have lavet en 3. arm der var sc. Men det forsøg er måske planlagt længe inden sc var alvor.

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                        • BulderB Offline
                          BulderB Offline
                          Bulder
                          wrote on sidst redigeret af
                          #732

                          Det kunne man. Og det er også set at man senere har tilføjet en ny arm med sc-dosering. Men spørgsmålet er om NCI overhovedet har interesse idet. Det koster jo.

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                          • nohopeN Offline
                            nohopeN Offline
                            nohope
                            wrote on sidst redigeret af
                            #733

                            Hvis de gerne vil sælge løsningen med Dara, så har de da det.

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                            • BulderB Offline
                              BulderB Offline
                              Bulder
                              wrote on sidst redigeret af
                              #734

                              Nu er NCI ikke kommerciel. Og i første omgang er formålet at vurdere sikkerheden og finde optimal dosis Veneto. Som sagt kan et senere fase 3 uden problemer anvende sc. Sc er standard og på gaden længe inden de når så langt.

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                              • nohopeN Offline
                                nohopeN Offline
                                nohope
                                wrote on sidst redigeret af
                                #735

                                Okej - men sc er stadig en mere operationel løsning - uanset om NCI tjener på det eller ej.

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                                • E Offline
                                  E Offline
                                  E_L
                                  wrote on sidst redigeret af
                                  #736

                                  On the SITC abstracts @peter12 linked to last week (pdf https://higherlogicdownload.s3.amazonaws.com/SITCANCER/7aaf41a8-2b65-4783-b86e-d48d26ce14f8/UploadedImages/Annual_Meeting_2018/Annual_Meeting/SITC_2018_Abstract_Book.pdf ) P5 also interesting Anti-CD38 immunotherapy kills Treg
                                  (CD4+CD25+FoxP3+CD38hi) and Breg
                                  (CD19+CD24+CD38hi) cells and restores the antitumor
                                  T-cell repertoire in chronic lymphocytic
                                  leukemia (CLL).

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                                  0
                                  • E Offline
                                    E Offline
                                    E_L
                                    wrote on sidst redigeret af
                                    #737

                                    Conclusions
                                    Anti-CD38 immunotherapy is lethal to
                                    immunosuppressive CD38hi Breg/Treg cells and may
                                    improve anti-tumor T-cells function via modulating
                                    CLL immune-microenvironment. The results of these
                                    analyses have led to the approval of a phase-II
                                    clinical study that will be testing Dara in
                                    relapsed/refractory CLL patients.

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                                    • J Offline
                                      J Offline
                                      JKY_VH
                                      wrote on sidst redigeret af
                                      #738

                                      Tak E L

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                                      • P Offline
                                        P Offline
                                        peter12
                                        wrote on sidst redigeret af
                                        #739

                                        Lidt ekko fra i torsdags https://legeforeningen.no/Fagmed/Norsk-selskap-for-hematologi/Nyheter/2018/Uke-43-Dara-ved-immunologisk-erytrocyttaplasi/

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                                        • SolsenS Offline
                                          SolsenS Offline
                                          Solsen
                                          wrote on sidst redigeret af
                                          #740

                                          Det lyder spændende !

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