- cafead   Apr 14, 2020 at 09:52: AM
via FDA has put Alnylam’s RNAi treatment for the polyneuropathy of hereditary transthyretin-mediated (hATTR) amyloidosis on its regulatory fast track. Alnylam secured the designation for the candidate, vutrisiran, ahead of the anticipated readout from a phase 3 trial early next year.
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