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Alnylam Receives Positive CHMP Opinion for Vutrisiran for the Treatment of ATTR Amyloidosis with Cardiomyopathy

1. Alnylam's vutrisiran receives positive opinion from EMA CHMP for ATTR-CM treatment.

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Why Very Bullish?

A positive EMA opinion may lead to market approval, potentially increasing revenue, as seen with past drug approvals by Alnylam, significantly boosting stock value.

How important is it?

The approval of vutrisiran can enhance Alnylam's growth and stability, positively impacting its stock.

Why Short Term?

If approval follows soon, immediate market reaction and increased sales could occur.

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CAMBRIDGE, Mass.--(BUSINESS WIRE)--Alnylam Pharmaceuticals, Inc. (Nasdaq: ALNY), the leading RNA interference (RNAi) therapeutics company, today announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has adopted a positive opinion recommending approval of its RNAi therapeutic vutrisiran for the treatment of wild type or hereditary transthyretin amyloidosis in adult patients with cardiomyopathy (ATTR-CM). ATTR-CM is a debilitating, rapidly.

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