Genmab — December 2025
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FDA Proactively Awards National Priority Voucher Based on Strong Phase 3 Study Results
For Immediate Release:
December 15, 2025The U.S. Food and Drug Administration today awarded a national priority voucher to teclistamab in combination with daratumumab for relapsed/refractory multiple myeloma. https://www.fda.gov/news-events/press-announcements/fda-proactively-awards-national-priority-voucher-based-strong-phase-3-study-results
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Cami still manages an article in Blood... Camidanlumab tesirine for relapsed or refractory classic Hodgkin lymphoma: a phase 2 study https://ashpublications.org/bloodadvances/article/9/23/6205/546723/Camidanlumab-tesirine-for-relapsed-or-refractory
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small new trial - Phase I/II Trial of ONC-PluReceptor NK Cells With Epcoritamab and Tafasitamab for Patients With Recurrent or Refractory B-cell Non-Hodgkin Lymphoma https://clinicaltrials.gov/study/NCT07283679
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Genmab får løftet kursmålet til 2900 kr. hos Kempen https://proinvestor.com/investornyt/1394515/genmab-far-loftet-kursmalet-til-2900-kr-hos-kempen
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Genmabs partner får udvidet godkendelse til lungekræftmiddel fra FDA https://proinvestor.com/investornyt/1394808/genmabs-partner-far-udvidet-godkendelse-til-lungekraeftmiddel-fra-fda
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subcutaneous - U.S. FDA Approval of RYBREVANT FASPRO
(amivantamab and hyaluronidase-lpuj) Enables the Simplest, Shortest Administration Time for a First-Line Combination Regimen when combined with LAZCLUZE
(lazertinib) https://www.jnj.com/media-center/press-releases/u-s-fda-approval-of-rybrevant-faspro-amivantamab-and-hyaluronidase-lpuj-enables-the-simplest-shortest-administration-time-for-a-first-line-combination-regimen-when-combined-with-lazcluze-lazertinib -
RAINFOL-05 ! New trial - Study to Assess the Efficacy and Safety of Rina-S in Participants With Non-small Cell Lung Cancer https://clinicaltrials.gov/study/NCT07288177
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Genmab’s Rina-S: New Study Targets Lung Cancer with Innovative Treatment https://www.tipranks.com/news/company-announcements/genmabs-rina-s-new-study-targets-lung-cancer-with-innovative-treatment
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Kort video: De amerikanske aktier, som er lokomotivet for det globale aktiemarked, har været negative de sidste fire-fem dage. Helge Larsen fortæller om årsagerne og kigger derudover selskabsspecifikt på Anavex, som skal til reeksamen, Bavarian Nordics fremtid, opdatering på Novo Nordisk og Genmab, og til sidst Zealand Pharma, hvor der torsdag er Q&A med CEO Adam Steensberg https://proinvestor.com/boards/130406
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yesterday : Pyxis Oncology Announces Positive Preliminary Phase 1 Data for Micvotabart Pelidotin (MICVO) in Recurrent/Metastatic Head and Neck Squamous Cell Carcinoma https://ir.pyxisoncology.com/news-releases/news-release-details/pyxis-oncology-announces-positive-preliminary-phase-1-data --> PYXS fell 48% on this
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How Adding epcoritamab to standard second-line therapy improves follicular lymphoma outcomes https://healthmedicinet.com/hmn-2025-how-adding-epcoritamab-standard-line-therapy/ "We will not know for a long time if [this regimen] is curative, but it’s certainly the beginning of a bright era for chemo-free therapy for follicular lymphoma.”
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Juleaftensdag holder Proinvestor redaktion for en sjælden gangs skyld fri. Vi er på igen torsdag 1. juledag med optagelse og udsendelse af Ugevideoen samt nyhedsbrev med fyldig omtale og perspektivering af Novos tidlige julegave med FDA´s godkendelse af Wegovy vægttabstablet. 2. juledag fredag byder vi på denne længere video-julespecial hvor jeg tager Larsen en nørdet snak med Pila Pharma’s grundlægger og forskningsdirektør, Dorte X. Gram - om hendes tid som forsker hos Novo Nordisk
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Du kommer med i kulissen bag udviklingen fedmemidler, opdagelsen af semaglutid og de helt spæde GLP-1 skridt på Novo Nordisk!
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Promising Therapy for Hard-to-treat DLBCL: Epcoritamab + GemOx #DLBCL | Joshua Brody, MD | #ASH2025 https://www.youtube.com/watch?v=HxPPVK6DJWs
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J&J-data giver særbehandling fra FDA-chef https://proinvestor.com/investornyt/1397504/ugens-grafik-2-jampj-data-giver-saeligrbehandling-fra-fda-chef
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