Genmab — November 2017
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Novod skrev bl.a. efter Q3 "ALCYONE ph III data likely at ASH; Dara now to be tested in RA
Genmab also noted it is hopeful that the Darzalex ph III ALCYONE
frontline data will be included for a late-breaking presentation at ASH in
December. Furthermore, we find it interesting that JnJ has filed an
Investigational New Drug (IND) application to start testing of Darzalex in
rheumatoid arthritis, which is a completely new space for the drug." -
Iøvrigt må en ekstra sjov lille ting - der var en som linkede til en artikel, hvor det blev nævnt at behandling med PD-1/PD-L1 kan give autoimmune sygdomme såsom leddegigt, så endnu en grund til at bruge dara i kombi med checkpoint - så gør man lidt ved gigten samtidig (måske)
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Late Breaking må vel komme her når den er frigivet. http://www.hematology.org/Annual-Meeting/Abstracts/2853.aspx
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som jeg forstår det, så var den 14. kun godkendelse som kvalificeret, men her snart udvælges 6. Man kunne vel forestille sig af der er flere end 6 kvalificerede ansøgere, så vi kan skuffes her om lidt. Jeg ser jeres og Novod's optimisme, men vi kan vel endnu ikke være sikre Jeg håber det bedste, har stadig masser af GEN
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Genmab Announces European Regulatory Submission for Daratumumab in Front Line Multiple Myeloma
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• Application to broaden label for daratumumab in front line multiple myeloma submitted to EMA
• Submission based on data from Phase III ALCYONE study
• Genmab to receive USD 3 million in milestone payments from Janssen -
"We are very pleased about this submission, which marks the first application for the use of daratumumab for patients with newly diagnosed multiple myeloma. We look forward to working with both Janssen and the EMA so that daratumumab can potentially become available for a broader group of multiple myeloma patients," said Jan van de Winkel, Ph.D., Chief Executive Officer of Genmab.
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