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Genmab — September 2015

Planlagt Fastgjort Låst Flyttet Genmab
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  • investor1989I Offline
    investor1989I Offline
    investor1989
    wrote on sidst redigeret af
    #2080

    Nogen der har overblik over hvad en fremskyndet CHMP proces er?

    1 Reply Last reply
    0
    • 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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      0
      • 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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          0
          • investor1989I Offline
            investor1989I Offline
            investor1989
            wrote on sidst redigeret af
            #2084

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

            1 Reply Last reply
            0
            • 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

              1 Reply Last reply
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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

                1 Reply Last reply
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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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                    0
                    • 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

                      1 Reply Last reply
                      0
                      • MadsSkjernM Offline
                        MadsSkjernM Offline
                        MadsSkjern
                        wrote on sidst redigeret af
                        #2090

                        præcis. og OPdivos hurtige approval var i 2.indikation

                        1 Reply Last reply
                        0
                        • 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

                              1 Reply Last reply
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                              • BulderB Offline
                                BulderB Offline
                                Bulder
                                wrote on sidst redigeret af
                                #2094

                                ... og så er vi henne ved juletid

                                1 Reply Last reply
                                0
                                • 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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                                        0
                                        • 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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