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EMA approval · 2025-03-25

EMA Authorised: Onpattro (patisiran sodium) — Alnylam Netherlands B.V.

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Summary

The European Medicines Agency authorised Onpattro (patisiran) for familial hereditary transthyretin-mediated amyloidosis with orphan designation and accelerated…

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Diseases / indications

Drugs mentioned

  • Onpattro (patisiran)

Snippet

Status: Authorised. Therapeutic area: Amyloidosis, Familial. MAH: Alnylam Netherlands B.V.. Decision date: 24/03/2025. Orphan medicine. Accelerated assessment