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Reading: Alnylam’s patisiran, the first ever FDA- and European Commission-approved RNAi therapeutic
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Life Science Newswire Service™ (LS) > Blog > Life Sciences > Pharma & Biopharma > Alnylam’s patisiran, the first ever FDA- and European Commission-approved RNAi therapeutic
Pharma & Biopharma

Alnylam’s patisiran, the first ever FDA- and European Commission-approved RNAi therapeutic

By Newsroom
Last updated: May 3, 2025
1 Min Read
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Lipid nanoparticle structure

On August 10, 2018, Alnylam Pharmaceuticals (Cambridge, MA) announced the first-ever FDA approval of an RNAi (RNA interference) drug. The drug is Alnylam’s patisiran, which is indicated for the treatment of polyneuropathy due to transthyretin-mediated amyloidosis (ATTR). ATTR is a rare inherited, debilitating, and often fatal disease caused by mutations in the transthyretin (TTR) gene. Patisiran is trade-named “Onpattro”. The FDA approved patisiran for the treatment of polyneuropathy in adults with hereditary transthyretin-mediated amyloidosis (hATTR) in adults.

On August 30, 2018 Alnylam announced that…



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