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FDA Approves Qfitlia™ (fitusiran), the First siRNA (RNAi Therapeutic) for the Treatment of Hemophilia A or B

1. Alnylam's Qfitlia™ is FDA-approved, the sixth RNAi drug by the company. 2. Qfitlia™ uniquely lowers antithrombin to enhance blood coagulation, preventing bleeds.

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Why Very Bullish?

The FDA approval of Qfitlia™ significantly boosts Alnylam's product pipeline, similar to past approvals that drove high market value increases.

How important is it?

The FDA's endorsement strengthens Alnylam's market position and investor confidence, critical for stock valuation.

Why Short Term?

Immediate market reactions to drug approvals typically influence stock prices quickly, as seen with previous Alnylam therapies post-approval.

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CAMBRIDGE, Mass.--(BUSINESS WIRE)--Alnylam Pharmaceuticals, Inc. (Nasdaq: ALNY), the leading RNAi therapeutics company, today highlighted the significance of the U.S. Food and Drug Administration's (FDA) approval of Qfitlia™ (fitusiran), the sixth Alnylam-discovered RNAi therapeutic approved in the U.S., and the first and only therapeutic to lower antithrombin (AT), a protein that inhibits blood clotting, with the goal of promoting thrombin generation to rebalance hemostasis and prevent bleeds.

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