Alnylam's Phase III Results For Vutrisiran Are 'Foundation' For Amyloidosis Expansion

FDA Filing Anticipated In Early 2021

The results are in for hATTR amyloidosis with polyneuropathy, while results for hereditary and wild-type ATTR with cardiomyopathy are expected later this year.

nerve cells, concept for neurodegenerative and neurological disease
Alnylam announces positive Phase III results for vutrisiran in hATTR amyloidosis with polyneuropathy. • Source: Shutterstock

Alnylam Pharmaceuticals Inc. anticipates that vutrisiran will become an attractive option for new hereditary transthyretin-mediated (hATTR) amyloidosis patients with its more convenient dosing, but it does not think that will undercut its approved drug Onpattro (patisiran).

The Cambridge, MA-based company announced on 7 January successful topline results from the Phase III HELIOS-A study of vutrisiran in hATTR amyloidosis with polyneuropathy, with the study meeting all of its primary and secondary endpoints at nine months

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