Genmab — December 2023
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En ting jeg aldrig rigtig har forstået: Hvis jnj vælger ikke at opte in, har Genmab forpligtet sig til ikke at udvikle hex38 i MM og Amy, hvor Dara er godkendt. Hvis Genmab taber voldgiftsappellen, kunne jnj fristes til ikke at opte in, fordi der venter en royaltyfri årrække. Og så står Genmab for alvor med håret i postkassen. Jeg begriber ikke, at Genmab er gået med på de betingelser, men det kan nogen måske forklare?
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@Klaussen old dara agreement stipulates how "Janssen shall use Commercially Reasonable Efforts to Develop, Manufacture and Commercialise Licensed Product" - you can assume this to be the same for HexaCD38 https://www.sec.gov/Archives/edgar/data/1434265/000104746919003334/a2238822zex-10_1.htm
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Det må koste på CSR-kontoen, hvis man spænder ben for færdigudviklingen af et præparat der er markant bedre end Dara. Jeg tror de skyder sig selv i foden, hvis de gør det, og forhåbentlig bliver de overhalet indenom af konkurrenterne. Så nej, det forestiller jeg mig ikke vil ske.
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The Lancet Haematology
@TheLancetHaem
Won Seog Kim presents data from the EPCORE NHL-5 dose escalation and expansion trial testing the bispecific antibody epcoritamab plus lenalidomide in patients with r/r DLBCL. One DLT (neutropenia) was observed (primary endpoint). ORR was 71.9% and CR was 53.1% #ASH23 https://twitter.com/TheLancetHaem/status/1733924588126666831 -
Genmab har lovende resultater med kræfthåb i svært behandlelig lymfekræft https://www.proinvestor.com/investornyt/1088770/genmab-har-lovende-resultater-med-kraefthab-i-svaert-behandlelig-lymfekraeft
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Multiple Myeloma Hub
@MM_Hub
CONGRESS | #ASH23 | Efstathios Kastritis
@uoaofficial
discusses the safety and efficacy results of daratumumab monotherapy in ND 3B LC AL from the EMN22 trial. 6-month OS rate was 65% and a haematological response in 77.5% of pts -- AL Amyloidosis--
https://twitter.com/MM_Hub/status/1733959437386215879 -
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