20 September 2022 - Amvuttra demonstrated halting or reversal in neuropathy impairment with subcutaneous administration once every three months.
Alnylam Pharmaceuticals today announced that the European Commission has granted marketing authorisation for Amvuttra (vutrisiran), an RNAi therapeutic for the treatment of hereditary transthyretin-mediated amyloidosis in adult patients with stage 1 or stage 2 polyneuropathy.