Almost a month ahead of schedule, the U.S. Food and Drug Administration has approved Alnylam Pharmaceuticals’ Amvuttra (vutrisiran) for the treatment of hereditary transthyretin-mediated amyloidosis (hATTR) with polyneuropathy in adults.
https://www.pharmalive.com/wp-content/uploads/2022/06/BioSpaceAlnylamCEO6-14-2022.jpg350625BioSpacehttps://www.pharmalive.com/wp-content/uploads/2020/01/Pharmalive_4c-300x37.pngBioSpace2022-06-14 11:42:542022-06-14 12:06:21Alnylam scores another FDA nod in hATTR