Genmab — Oktober 2020
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Aktier/tendens: Vestas og DSV i fokus i nervøst marked: https://www.proinvestor.com/investornyt/669096/aktier-tendens-vestas-og-dsv-i-fokus-i-nervost-marked
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Daratumumab efficacy in extramedullary orbital myeloma https://onlinelibrary.wiley.com/doi/full/10.1002/ccr3.3458
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AMGEN: KYPROLIS
(carfilzomib) sales decreased 2% year-over-year driven by volume declines, as fewer new patients began treatment due to COVID-19. Early indications point to a strong launch of the new once-weekly KYPROLIS and DARZALEX
(daratumumab) combination regimen that was approved by the U.S. Food and Drug Administration (FDA) in August. -
Efficacy and safety of weekly carfilzomib (70 mg/m2), dexamethasone, and daratumumab (KdD70) is comparable to twice-weekly KdD56 while being a more convenient dosing option: a cross-study comparison of the CANDOR and EQUULEUS studies https://www.tandfonline.com/doi/full/10.1080/10428194.2020.1832672
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A global antiB cell strategy combining obinutuzumab and daratumumab in severe pediatric nephrotic syndrome https://link.springer.com/article/10.1007/s00467-020-04811-0
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Novartis is also starting a new trial for people with relapsing MS who switch to Kesimpta from another anti-CD20 monoclonal antibody therapy; ie. Ocrevus https://clinicaltrials.gov/ct2/show/NCT04486716
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In addition, Novartis is exploring other avenues for Kesimpta’s clinical development, including plans to test the medication in children with MS. https://multiplesclerosisnewstoday.com/news-posts/2020/09/10/new-and-ongoing-trials-evaluating-kesimpta-including-as-switch-therapy/ “We are not stopping research into Kesimpta,” he added. “Research continues with Kesimpta to help more patients know of its value.”
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Sarclisa
was approved in March in the U.S. for the treatment of adults with relapsed refractory multiple myeloma (RRMM) who have received at least two prior therapies including lenalidomide and a proteasome inhibitor and in June by the European Commission in certain adults with RRMM. Third-quarter Sarclisa
sales were €13 million of which €9 million was generated in the U.S. despite the challenging launch environment due to COVID-19. Sarclisa
is now launched in the U.S., Austria, Japan, -
Thanks to @EL for pushing news feed today. The markets seems to appreciate the flow

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@E L
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Sr
y for the last 2 posts - originally regards to E L -
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God morgen .-)
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