Home » News » Alnylam receives EU approval for RNAI medication for the treatment of transthyretin-amyloidosis with cardiomyopathy

Alnylam receives EU approval for RNAI medication for the treatment of transthyretin-amyloidosis with cardiomyopathy

Breaking News: Alnylam Pharmaceuticals Receives EU Approval for RNAI Medication

June 9, 2025 – 12:58 PM

EU Approval Drives Stock Surge

In a major breakthrough for the biopharmaceutical industry, Alnylam Pharmaceuticals, Inc. has received approval from the European Union for its RNA interference (RNAi) medication designed to treat transthyretin-amyloidosis with cardiomyopathy. This significant development has propelled the company’s stock price to new heights, with shares surging by 1.12% to $304.20 USD.

What is Transthyretin-Amyloidosis?

Transthyretin-amyloidosis is a progressive and potentially life-threatening condition characterized by the abnormal buildup of transthyretin protein in various tissues throughout the body. This buildup can lead to severe health complications, including cardiomyopathy, a disease of the heart muscle that affects its ability to pump blood effectively.

About Alnylam Pharmaceuticals

Alnylam Pharmaceuticals is a leading biopharmaceutical company specializing in the discovery, development, manufacture, and marketing of new therapeutic agents based on RNA interference (RNAi). Their portfolio includes AMVUTTRA (Vutrisiran) for the treatment of hereditary transthyretine-mediated amyloid (HATTR) with polyneuropathy in adults, Onpattro (Patisiran) for the treatment of polyneuropathy of HATTR-Amyloidosis in adults, and several other innovative treatments.

Expert Insights and Future Implications

Dr. Phillip D. Zamore, a distinguished scientist in the field of RNAi, has been appointed to Alnylam’s Scientific Advisory Board. This appointment underscores the company’s commitment to advancing cutting-edge research and innovation. As Alnylam continues to expand its portfolio, experts anticipate significant advancements in the treatment of various genetic disorders, potentially transforming the healthcare landscape.

Stock Performance and Analyst Ratings

The recent EU approval has not only boosted investor confidence but also garnered positive ratings from financial analysts. UBS has issued a buy rating, and BofA Securities has retained a positive outlook on the company’s stock. These endorsements reflect the strong market potential and Alnylam’s leadership in the biopharmaceutical sector.

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