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Genmab — Juli 2020

Planlagt Fastgjort Låst Flyttet Genmab
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  • E Offline
    E Offline
    E_L
    wrote on sidst redigeret af
    #987

    from 2019 : Janssen DuoBody Collaboration
    In July 2012, we entered into a collaboration with Janssen to create and develop bispecific antibodies using our DuoBody platform. Under this agreement, Janssen received an exclusive worldwide license to use the DuoBody technology to create panels of bispecific antibodies (up to 10 DuoBody programs) to multiple disease target combinations. We recorded an upfront payment of $3.5 million from Janssen and will potentially be entitled to milestone and

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    • E Offline
      E Offline
      E_L
      wrote on sidst redigeret af
      #988

      and license payments of up to approximately $175.0 million, as well as royalties for each commercialized DuoBody product. Janssen may terminate this agreement in whole or with respect to any particular target binding pair upon providing 120 days' prior written notice to us in accordance with the terms of the agreement.

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      • E Offline
        E Offline
        E_L
        wrote on sidst redigeret af
        #989

        Under the terms of a December 2013 amendment, Janssen was entitled to work on up to 10 additional programs. In exchange, we recorded an initial payment of $2.0 million from Janssen and are potentially entitled to receive average milestone and license payments of approximately $191.0 million if Janssen successfully initiates, develops and commercializes all such additional programs. In addition, we will be entitled to royalties on net sales of any commercialized products.

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        • E Offline
          E Offline
          E_L
          wrote on sidst redigeret af
          #990

          As of March 31, 2019, Janssen has exercised 14 licenses under this collaboration and we have recorded $60.0 million in milestone payments to date. No further options remain for potential use by Janssen. Six product candidates are currently in clinical development by Janssen under this agreement.

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          • E Offline
            E Offline
            E_L
            wrote on sidst redigeret af
            #991

            i think that is all the public info there is, except for some comments by Jan on the royalty %

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            • SolsenS Offline
              SolsenS Offline
              Solsen
              wrote on sidst redigeret af
              #992

              Amivantamab has to be developed under the first deal. So $175 mln in milestones - dont think any triggered milestone connected to ph3 will make a difference.

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              • SolsenS Offline
                SolsenS Offline
                Solsen
                wrote on sidst redigeret af
                #993

                What matters is data and potential royalty.

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                • G Offline
                  G Offline
                  GeorgeBest
                  wrote on sidst redigeret af
                  #994

                  Do we know if this amivantamab/lazertinib kombo is targetting first line lung cancer patients?

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                  • SolsenS Offline
                    SolsenS Offline
                    Solsen
                    wrote on sidst redigeret af
                    #995

                    Indtil videre er det kun NSCLC med Exon 19 mutationen forsøgene går efter. Jeg mener, at det er 15-20% af hele NSCLC populationen - herunder first line. https://mc.vanderbilt.edu/ckm/gl/mutation_profiles/pdfopen.php?fnp=lung_cancer/content/EGFR/Lung_Cancer_and_EGFR_Exon_19_Deletions.pdf

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                    • BulderB Offline
                      BulderB Offline
                      Bulder
                      wrote on sidst redigeret af
                      #996

                      A Phase 3, Randomized Study of Amivantamab and Lazertinib Combination Therapy Versus Osimertinib Versus Lazertinib as First-Line Treatment in Patients With EGFR-Mutated Locally Advanced or Metastatic Non-Small Cell Lung Cancer.

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                      • G Offline
                        G Offline
                        GeorgeBest
                        wrote on sidst redigeret af
                        #997

                        Tak for svar til Solsen og Bulder 🙂

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                        • BulderB Offline
                          BulderB Offline
                          Bulder
                          wrote on sidst redigeret af
                          #998

                          About 20 percent of NSCLC cases have somatic EGFR mutations. (15) Patients with the two most common mutations, EGFR L858R and EGFR exon deletion 19, are treated with EGFR-tyrosine kinase inhibitors (EGFR-TKIs), which include erlotinib, gefitinib, afatinib, dacomitinib, and osimertinib. https://www.mskcc.org/clinical-updates/systemic-therapy-locally-advanced-and-metastatic-non-small-cell-lung

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                          • E Offline
                            E Offline
                            E_L
                            wrote on sidst redigeret af
                            #999

                            Amgen dumps early-stage CD38xCD3 bispecific, returning rights to Xencor https://endpts.com/amgen-dumps-early-stage-cd38xcd3-bispecific-returning-rights-to-xencor-picked-up-in-2015-alliance/

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                            • K Offline
                              K Offline
                              Klarussen
                              wrote on sidst redigeret af
                              #1000

                              Ser teknisk svag ud på kort sigt efter 23. julis brud af optrendslinien fra midtmarts,
                              støtte omkring 2000-området.

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                              • S Offline
                                S Offline
                                Sukkeralf
                                wrote on sidst redigeret af
                                #1001

                                Så fik Jan ret i at CD3 var en dårlig kombi med CD38 ????

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                                • E Offline
                                  E Offline
                                  E_L
                                  wrote on sidst redigeret af
                                  #1002

                                  not sure, when did he say that? JNJ is trying Dara with Teclistamab and Sanofi is experimenting with a tri-specific:
                                  Anti CD38-CD28-CD3

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                                  • SolsenS Offline
                                    SolsenS Offline
                                    Solsen
                                    wrote on sidst redigeret af
                                    #1003

                                    JW said that CD3 was not the chosen combo with CD38. Dont remember why.

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                                    • SolsenS Offline
                                      SolsenS Offline
                                      Solsen
                                      wrote on sidst redigeret af
                                      #1004

                                      Remember some of us was worried that Xencor where chosen as bispecific partner by Amgen - Genmab is best in class 😉

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                                      • J Offline
                                        J Offline
                                        Jedi
                                        wrote on sidst redigeret af
                                        #1005

                                        I don’t think a combo of two molecules (Dara and Teclistamab) can be compared to a single bispecific CD3 x CD38 agent

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                                        • J Offline
                                          J Offline
                                          Jedi
                                          wrote on sidst redigeret af
                                          #1006

                                          ...and yes, good to see that Xencor did not have success with a bispecific that
                                          Gen is not pursuing:-)

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