Alnylam receives European Commission approval for Amvuttra (vutrisiran) for the treatment of ATTR amyloidosis with cardiomyopathy

Alnylam Pharmaceuticals

9 June 2025 - Decision follows recent authorisations in the US and Brazil.

Alnylam Pharmaceuticals today announced that the European Commission has granted approval for the treatment of wild type or hereditary transthyretin amyloidosis in adult patients with cardiomyopathy.

Read Alnylam Pharmaceuticals press release

Michael Wonder

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Michael Wonder

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Outcome , Medicine , Europe , Registration