Vutrisiran Now Under Review for Approval in Europe for FAP Treatment

Vutrisiran Now Under Review for Approval in Europe for FAP Treatment

306541

Vutrisiran Now Under Review for Approval in Europe for FAP Treatment

The European Medicines Agency (EMA) has agreed to review Alnylam Pharmaceuticals’ application requesting the approval of vutrisiran, its second-generation RNA interference (RNAi) therapy candidate for familial amyloid polyneuropathy (FAP). Hereditary ATTR (hATTR) amyloidosis, which includes FAP, “is a rare, rapidly progressive, debilitating and fatal condition and we are delighted that the EMA has agreed to review the regulatory submission for vutrisiran based on the positive 9-month data from the HELIOS-A Phase 3 study,” Rena Denoncourt, vice…

You must be logged in to read/download the full post.