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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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