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Genmab — September 2015

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
    #2081

    optimisation of the assessment timetable by better balancing evaluation phases to reach a CHMP opinion within the 150 days after the start of a marketing authorisation application procedure (compared to 210 days in non-accelerated procedures);

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    • investor1989I Offline
      investor1989I Offline
      investor1989
      wrote on sidst redigeret af
      #2082

      Taler vi så 8 måneder, 10 måneder eller lignende i stedet for 12-13 ?

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      0
      • G Offline
        G Offline
        gentogen
        wrote on sidst redigeret af
        #2083

        http://www.ema.europa.eu/ema/index.jsp?curl=pages/news_and_events/news/2015/07/news_detail_002381.jsp&mid=WC0b01ac058004d5c1

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        • investor1989I Offline
          investor1989I Offline
          investor1989
          wrote on sidst redigeret af
          #2084

          150 dage dvs. maks 6 måneder fra i dag af eller fra indsendelse?

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          • dingleberryD Offline
            dingleberryD Offline
            dingleberry
            wrote on sidst redigeret af
            #2085

            forskellen mellem BLA og NDA er om det er biologisk materiale eller et "almindeligt" compound

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            • investor1989I Offline
              investor1989I Offline
              investor1989
              wrote on sidst redigeret af
              #2086

              Man skal dog huske at fra CHMP kommer med en anbefaling går der oftest 1-2 måneder før den endelige approval og derefter 2-3 måneder før man har godkendelser i de enkelte lande + tilskud osv. på plads

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              • investor1989I Offline
                investor1989I Offline
                investor1989
                wrote on sidst redigeret af
                #2087

                Men jannsen har nok en hurtig og smidig maskine her

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                • investor1989I Offline
                  investor1989I Offline
                  investor1989
                  wrote on sidst redigeret af
                  #2088

                  new drug application og biologic license application ?

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                  • dingleberryD Offline
                    dingleberryD Offline
                    dingleberry
                    wrote on sidst redigeret af
                    #2089

                    det lille "s" står for om det er supplementary - dvs om der allerede er givet en approval fra FDAs side i en anden indikation

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                    • MadsSkjernM Offline
                      MadsSkjernM Offline
                      MadsSkjern
                      wrote on sidst redigeret af
                      #2090

                      præcis. og OPdivos hurtige approval var i 2.indikation

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                      • dingleberryD Offline
                        dingleberryD Offline
                        dingleberry
                        wrote on sidst redigeret af
                        #2091

                        så en sBLA burde alt andet lige være hurtigere end en BLA. Og pga produktionsprocessen vil en NDA være hurtigere end en BLA

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                        0
                        • dingleberryD Offline
                          dingleberryD Offline
                          dingleberry
                          wrote on sidst redigeret af
                          #2092

                          Siden dara er en BLA vil den principielt være i den langsomme gruppe - modsat vil den blive hurtigere pga unmet need

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                          • dingleberryD Offline
                            dingleberryD Offline
                            dingleberry
                            wrote on sidst redigeret af
                            #2093

                            Så vidt jeg kan gennemskue er Opdivo's godkendelse af BLA (den første gang) den hurtigste godkendelse - 3 måneder før pdufa

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                            0
                            • BulderB Offline
                              BulderB Offline
                              Bulder
                              wrote on sidst redigeret af
                              #2094

                              ... og så er vi henne ved juletid

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                              • G Offline
                                G Offline
                                gentogen
                                wrote on sidst redigeret af
                                #2095

                                Conditional marketing authorisation allows for the early approval of a medicine on the basis of less complete clinical data than normally required, if the medicine addresses an unmet medical need and targets a seriously debilitating or life-threatening disease

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                                0
                                • G Offline
                                  G Offline
                                  gentogen
                                  wrote on sidst redigeret af
                                  #2096

                                  Link Preview Image
                                  Page or document not found | European Medicines Agency (EMA)

                                  We are sorry, but the content you tried to access is unavailable at the link you used, which was either incorrect or out-of-date. To help you find what you are looking for, we have included some useful tips.

                                  favicon

                                  European Medicines Agency (EMA) (www.ema.europa.eu)

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                                  • SolsenS Offline
                                    SolsenS Offline
                                    Solsen
                                    wrote on sidst redigeret af
                                    #2097

                                    NDA & BLA Application NDA and BLA are applications to market a new product. NDAs are used by CDER (center for drugs) and BLAs are used by CBER (center for biologics) – The BLA requires close scrutiny of the and facilities, because of the greater products. manufacturing process variability of biological – The application will include complete reports on all studies including patient listings, analysis according to the original statistical analysis protocol (SAP) as well as any exploratory analysi

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                                    • SolsenS Offline
                                      SolsenS Offline
                                      Solsen
                                      wrote on sidst redigeret af
                                      #2098

                                      original statistical analysis protocol (SAP) as well as any exploratory analysis.

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                                      • MadsSkjernM Offline
                                        MadsSkjernM Offline
                                        MadsSkjern
                                        wrote on sidst redigeret af
                                        #2099

                                        Opdivo tog fra 26/9 - 22/12 2014 fra accept til approval i melanoma

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                                        0
                                        • SolsenS Offline
                                          SolsenS Offline
                                          Solsen
                                          wrote on sidst redigeret af
                                          #2100

                                          http://www.slideshare.net/gas25/usfda-nda-vs-bla pkt 30 og frem

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