Genmab — December 2016
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http://borsen.dk/nyheder/virksomheder/artikel/1/336034/genmabs_kraeftmiddel_i_hovedrolle_paa_kraeftkonference.html Sikkert en gentagelse af Plesners syn på dara og ASH
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Det, vi kan se er, at vi efter at have fjernet bremsen i første omgang får et direkte drab af kræftceller af antistoffet. Herefter får vi en omstilling af immunsystemet, således at sygdommen i løbet af få måneder kommer under kontrol og går i ro,” siger han til Dagens Medicin - citat fra Børsen, som så citerer "Dagens Medicin"
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JNJ statement ved approval: "We are proud of the rapid development and approval of DARZALEX for use earlier in the treatment pathway, but our work does not stop here,” said Peter F. Lebowitz, M.D., Ph.D., Global Oncology Head, Janssen Research & Development, LLC. “We are only starting to uncover the full potential of this compound, and we remain committed to the continued study of daratumumab to more fully understand its utility for patients with multiple myeloma
and other cancer types.” -
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Kiggede lige hurtigt CMD prøsentationen igennem - og der var lige en slide som jeg ikke havde lagt mærke til. Ved ikke om det har været nævnt herinde tidligere, men man har i 2016 indledt forskningssamarbejde med CiMass, VLiNK Therapeutics og Imm Therapeutics - ikke så vigtigt lige nu, men da spændende hvis det munder ud i mere senere.
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Acetylon Presents Early Phase 1a/1b Results for Citarinostat (ACY-241) in Combination with Pomalyst
and Dexamethasone Showing Promising Treatment Responses in Relapsed or Relapsed-and-Refractory Multiple Myeloma http://www.businesswire.com/news/home/20161204005058/en/Acetylon-Presents-Early-Phase-1a1b-Results-Citarinostat -
Prøv linket igen
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Daratumumab associated with deep clinical response in relapsed, refractory multiple myeloma http://www.healio.com/
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Tak jkj og GB.
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Minimal residual disease (MRD) testing has become a standard assessment with the revised International Myeloma Working Group response criteria and was necessitated by the increasing efficacy of new therapies. These two trials are the first to evaluate MRD in the setting of relapsed disease. In the two studies, a high rate of MRD negativity has been observed, which has translated to longer PFS. The results are a testament to the efficacy of the drug in myeloma.
Shaji Kumar, MD
Mayo Clinic
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It is amazing to see that we can get MRD negativity in the relapsed space. Both of these combinations were approved in November.
Noopur Raje, MD
Massachusetts General Hospital Cancer Center
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