NICE u-turn sees Akcea’s Waylivra win NHS funding by Selina McKee | Sep 18, 2020 | News | 0 The drug is the first and only therapy for the ultra rare condition Familial Chylomicronaemia Syndrome (FCS) Read More
Akcea’s rare lipid disorder drug wins PIM status by Selina McKee | Oct 10, 2017 | News | 0 Akcea Therapeutics’s volanesorsen has been granted a Promising Innovative Medicine designation by the Medicines and Healthcare products Regulatory Agency for the treatment of familial chylomicronaemia syndrome, a rare genetic lipid disorder. Read More