Genmab — Juni 2016
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Fast Track is a designation by the United States Food and Drug Administration (FDA) of an investigational drug for expedited review to facilitate development of drugs which treat a serious or life-threatening condition and fill an unmet medical need. Fast Track designation must be requested by the drug company. The request can be initiated at any time during the drug development process. FDA will review the request and attempt to make a decision within sixty days.
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Ja tak til alle herinde syntes i er fantastiske at i deler ud af alt den viden i har nyder så meget at læse alt der bliver postet herinde og håber jeg selv engang kan bidrage men for nu tager jeg imod og ser frem til at kunne give tilbage TAK med ønske om gode nyheder i morgen forsat god weekend
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Om Pembrolizumab: https://en.wikipedia.org/wiki/Pembrolizumab
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Men der er adskillige studier i gang med Keytruda mod MM. https://www.clinicaltrials.gov/ct2/results?term=Keytruda+multiple+myeloma&Search=Search
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Heraf er der to fase 3 studier med pom-dex og rev-dex, som der nok skal holdes øje med. http://keynoteclinicaltrials.com/trials/blood-cancer
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Der kommer en oral præsentation af fase 1 Pem+len+dex på ASCO. (Keynote-023) Men altså endnu kun fase 1 safety. Abstract: http://abstract.asco.org/176/AbstView_176_167184.html
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Godmorgen. Paul Richardson glæder sig
også til daratumumab data idag, fra 7:35 https://youtu.be/TJdmxAoRSwI
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bliver spændende imorgen, kan det ikke tænkes data fra castor og pollux bliver bedre nu der er gået længere tid og