Alnylam Shares Surge on $730M Volume After FDA Approval Boosts Market Outlook and Analysts Raise Targets

Generated by AI AgentAinvest Market Brief
Monday, Aug 18, 2025 9:17 pm ET1min read
Aime RobotAime Summary

- Alnylam’s stock surged 1.77% on August 18, 2025, with a $730M trading volume, driven by FDA approval of Amvuttra for ATTR-CM treatment.

- Analysts raised price targets to $570–$470, citing Amvuttra’s cardiovascular mortality differentiation and $6.9B projected sales by 2035.

- Q2 revenue hit $469M, but net losses and a 4.1 debt-to-equity ratio highlight risks amid competition from Vyndamax and Attruby.

- High pricing ($480K/year) and reimbursement challenges could limit market share, though strong liquidity and institutional ownership support long-term growth.

Alnylam Pharmaceuticals (ALNY) rose 1.77% on August 18, 2025, with a trading volume of $730 million, up 129.95% from the previous day. The stock’s recent performance follows a pivotal FDA approval for Amvuttra (vutrisiran) to treat transthyretin-mediated amyloidosis (ATTR-CM) on March 20, 2025, expanding its therapeutic footprint and differentiating it from competitors with a label emphasizing cardiovascular mortality reduction. Analysts have revised price targets upward, with recent upgrades from H.C. Wainwright ($570) and J.P. Morgan ($475), reflecting confidence in the drug’s market potential and the company’s pipeline.

Alnylam’s financials highlight a mixed landscape. While Q2 2025 revenue reached $469 million, driven by $359 million in ATTR-related sales, the company reported a net loss of $0.32 per share. Despite this, gross profit margins remain strong at 83.64%, and liquidity metrics, including a current ratio of 2.8, suggest resilience. The ATTR-CM market, valued at over $6 billion, remains a focal point, with Amvuttra projected to capture a significant share as newly diagnosed patients transition from therapies like Pfizer’s Vyndamax. Analysts estimate Amvuttra sales could reach $6.9 billion by 2035, underpinned by its quarterly dosing regimen and clinical differentiation.

Risks persist, however. The company’s premium pricing strategy for Amvuttra ($480,000 annually) may face reimbursement hurdles, particularly with commercial insurers. Intensifying competition from BridgeBio’s Attruby and Pfizer’s Vyndamax could pressure market share, especially as real-world data on efficacy and safety evolve. Additionally, Alnylam’s debt-to-equity ratio of 4.10 and ongoing R&D investments pose near-term profitability challenges. Despite these headwinds, institutional ownership remains robust, with 93% held by funds, and analysts maintain a “Moderate Buy” consensus, citing long-term growth in rare disease therapeutics.

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