Source
Fierce Pharma
Despite growing competition in the transthyretin amyloid cardiomyopathy (ATTR-CM) field, Alnylam is hoping its RNA interference approach can set it apart from its peers. And now, the Massachusetts-based drugmaker has a fresh FDA approval to support its thesis.
The FDA has signed off on Alnylam’s Amvuttra, also known as vutrisiran, as a treatment for cardiomyopathy of wild-type or hereditary ATTR-CM in adults to reduce the chance of cardiovascular death, hospitalizations and urgent heart failure visits.
Thanks to a previous nod in 2022, Amvuttra is now the first medication approved in the U.S. to treat both ATTR-CM and polyneuropathy of hereditary transthyretin-mediated amyloidosis (hATTR-PN), Alnylam noted in a Thursday release.
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