Akcea Therapeutics and Ionis Pharmaceuticals have announced that their investigational therapy Waylivra (volanesorsen) has been recommended by the EMA’s Committee for Medicinal Products for Human Use (CHMP) for conditional marketing authorisation as a supplement to diet in genetically confirmed familial chylomicronaemia syndrome (FCS) in adult patients who have not responded adequately to diet and triglyceride lowering therapy and who are at high risk of pancreatitis.
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