Literature DB >> 35997942

Vutrisiran: First Approval.

Susan J Keam1.   

Abstract

Vutrisiran (AMVUTTRA™) is a subcutaneously administered transthyretin-directed small interfering ribonucleic acid (siRNA) therapeutic (also called RNA interference, or RNAi therapeutic) being developed by Alnylam Pharmaceuticals, Inc. for the treatment of amyloid transthyretin-mediated (ATTR) amyloidosis, including hereditary ATTR (hATTR) amyloidosis and wild-type ATTR (wtATTR) amyloidosis. Vutrisiran was approved in June 2022 in the USA for the treatment of the polyneuropathy of hATTR amyloidosis in adults and received a positive opinion in the EU in July 2022 for the treatment of hATTR amyloidosis in adult patients with stage 1 or stage 2 polyneuropathy. Vutrisiran is also under regulatory review for the treatment of the polyneuropathy of hATTR amyloidosis in adults in Japan and Brazil. This article summarizes the milestones in the development of vutrisiran leading to this first approval in hATTR amyloidosis.
© 2022. The Author(s), under exclusive licence to Springer Nature Switzerland AG.

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Year:  2022        PMID: 35997942     DOI: 10.1007/s40265-022-01765-5

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   11.431


  3 in total

1.  Impact of baseline polyneuropathy severity on patisiran treatment outcomes in the APOLLO trial.

Authors:  Dianna Quan; Laura Obici; John L Berk; Yukio Ando; Emre Aldinc; Matthew T White; David Adams
Journal:  Amyloid       Date:  2022-09-18       Impact factor: 6.571

Review 2.  RNA-targeting and gene editing therapies for transthyretin amyloidosis.

Authors:  Alberto Aimo; Vincenzo Castiglione; Claudio Rapezzi; Maria Franzini; Giorgia Panichella; Giuseppe Vergaro; Julian Gillmore; Marianna Fontana; Claudio Passino; Michele Emdin
Journal:  Nat Rev Cardiol       Date:  2022-03-23       Impact factor: 49.421

  3 in total

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