murteza schreef op 23 augustus 2018 01:26:
www.shire.com/en/newsroom/2018/april/...Lanadelumab Regulatory Status
U.S. Food and Drug Administration (FDA) accepted Shire's biologics license application (BLA) and granted priority review for lanadelumab in February 2018. The FDA is expected to provide a decision on lanadelumab by August 26, 2018, based on the Prescription Drug User Fee Act V action date.
European Medicines Agency (EMA) validated the marketing authorization application for lanadelumab in March 2018. EMA had previously granted lanadelumab an accelerated assessment reducing the number of evaluation days required, from 210 to 150.
Health Canada accepted the New Drug Submission (NDS) for lanadelumab under Priority Review in March 2018 shortening the review timeline from 300 to 180 days.
Therapeutic Goods Administration in Australia granted lanadelumab priority review and orphan drug designation in February 2018.
met alle respect, EMA is niet dommer dan FDA ... lana zal worden goedgekeurd, en dat is niet slecht nieeuws...
btw. een hollandse glorie medicijn komt op de markt en binnen twee jaar claimt 10 procent van hele de markt.. en later minimaal 20 procent van de markt, bij elkaar opgeteld 300 mil. omzet alleen van ruconest... een bedrijf die geen eens 1 miljaard waard is... wat verwachten jullie?