Alnylam (ALNY) Rises 6.0%: Could This Signal More Upside Ahead?
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Sep 10 2025
0mins
Source: NASDAQ.COM
Alnylam Pharmaceuticals Stock Performance: Alnylam Pharmaceuticals (ALNY) shares rose 6% to $482.13, driven by strong sales of its drug Amvuttra, which saw an 89% year-over-year growth, generating $801.9 million in global sales. The company is expected to report a quarterly earnings increase of 378% year-over-year.
Earnings Estimate Revisions: The consensus EPS estimate for Alnylam has been revised 46.4% higher in the last 30 days, indicating a positive trend that often correlates with stock price appreciation. The stock currently holds a Zacks Rank of #3 (Hold).
Foghorn Therapeutics Overview: Foghorn Therapeutics (FHTX) experienced a 5.6% decline in its stock price, with a consensus EPS estimate change of +6.7% for the upcoming report, reflecting a year-over-year change of +12.9%. It currently has a Zacks Rank of #2 (Buy).
AI Investment Insights: The article discusses the potential for significant wealth creation in the next phase of AI, suggesting that early investors in emerging companies may benefit as the growth of current AI stocks levels off. Zacks' report highlights four under-the-radar companies poised for success in AI's next wave.
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Analyst Views on ALNY
Wall Street analysts forecast ALNY stock price to rise
17 Analyst Rating
14 Buy
3 Hold
0 Sell
Strong Buy
Current: 313.040
Low
351.00
Averages
479.53
High
580.00
Current: 313.040
Low
351.00
Averages
479.53
High
580.00
About ALNY
Alnylam Pharmaceuticals, Inc. is a commercial-stage biopharmaceutical company. The Company is engaged in discovering, developing, manufacturing and commercializing novel therapeutics based on ribonucleic acid interference (RNAi). Its marketed products include AMVUTTRA (vutrisiran) for the treatment of the polyneuropathy of hereditary transthyretin-mediated amyloidosis (hATTR) in adults ; ONPATTRO (patisiran) for the treatment of the polyneuropathy of hATTR amyloidosis in adults; GIVLAARI (givosiran) for the treatment of adults with acute hepatic porphyria; OXLUMO (lumasiran) for the treatment of primary hyperoxaluria type 1, and Leqvio (inclisiran), which is being developed and commercialized by its partner, Novartis AG, for the treatment of adults with hypercholesterolemia or mixed dyslipidemia. The Company’s clinical development programs include Cemdisiran, Zilebesiran, Elebsiran, Mivelsiran, ALN-6400, and ALN-HTT02. It is developing Cemdisiran to treat complement-mediated diseases.
About the author
Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
Alnylam Pharmaceuticals Shares Drop 24%, Yet Optimism Persists
- Significant Revenue Growth: Alnylam Pharmaceuticals reported a 121% year-over-year surge in product revenue to $1.04 billion in Q1, primarily driven by a 153% increase in its ATTR franchise, indicating strong market demand in the rare disease treatment sector.
- Profitability Improvement: The company achieved earnings per share (EPS) of $1.51, a substantial turnaround from a loss of $0.14 per share in the same period last year, demonstrating Alnylam's rapid transition into a profitable commercial powerhouse, which boosts investor confidence.
- Expansion into New Indications: New data for Alnylam's Amvuttra reinforces its position as a first-line treatment for cardiomyopathy, setting the stage for a massive commercial launch and further market share expansion.
- Strong Technological Moat: Alnylam's RNA interference platform creates a deep technological moat, and its collaboration with Inceptive Nucleics on AI accelerates the discovery of next-generation RNAi structures, ensuring its competitive edge in the biotech industry.
See More
Alnylam Pharmaceuticals Reports Strong Q1 Performance
- Significant Revenue Growth: Alnylam Pharmaceuticals reported a 121% year-over-year surge in product revenue to $1.04 billion in Q1, primarily driven by a 153% increase in its transthyretin amyloidosis (ATTR) franchise, indicating strong market demand in the rare disease treatment sector.
- Profitability Improvement: The company achieved earnings per share (EPS) of $1.51, a substantial turnaround from a loss of $0.14 per share in the same period last year, marking a significant improvement in profitability and showcasing its transition from a high-burn clinical biotech to a profitable commercial powerhouse.
- Broad Market Outlook: Alnylam's guidance for full-year 2026 net product revenue ranges between $4.9 billion and $5.3 billion, reflecting a 71% year-over-year growth at the midpoint, highlighting the company's potential to penetrate mainstream high-volume therapeutic markets, particularly in cardiomyopathy and hypertension.
- Strong Technological Moat: Alnylam's RNA interference (RNAi) drug delivery system creates a deep technological moat, and its strategic AI collaboration with Inceptive Nucleics accelerates the discovery of next-generation RNAi structures, ensuring the company's competitive edge in the rapidly evolving biotech landscape.
See More
Komodo Expands Partnership with Alnylam to Enhance AI Decision-Making
- Partnership Expansion: Komodo Health has expanded its strategic partnership with Alnylam Pharmaceuticals to scale the Marmot analytics platform across key enterprise functions, enhancing AI-driven decision-making and improving overall operational efficiency.
- Real-Time Intelligence Transformation: The Marmot platform, built on the Healthcare Map, integrates over 330 million de-identified patient journeys, enabling Alnylam to break free from fragmented analytics and achieve real-time, transparent healthcare intelligence, significantly reducing reporting cycles from months to hours.
- New Feature Launch: Komodo has released new capabilities for Marmot aimed at making healthcare intelligence accessible to all users, ensuring that every analysis is reproducible and verifiable, thereby enhancing the scientific rigor and accuracy of decision-making while embedding AI into core enterprise processes.
- Industry Transformation Trend: This partnership reflects a broader shift in healthcare and life sciences, as organizations move beyond mere AI experimentation to adopt new operating models centered around real-time intelligence, addressing increasingly complex market demands.
See More
Regeneron's Cemdisiran Marketing Applications Accepted by U.S. and European Regulators
- Drug Application Progress: Regeneron (REGN) and Alnylam Pharmaceuticals (ALNY) have had their marketing applications for the experimental therapy cemdisiran accepted by U.S. and European regulators, marking a significant advancement in treating myasthenia gravis.
- Priority Review Approval: The U.S. FDA has issued a priority review for cemdisiran's New Drug Application with a target action date in November, which will expedite the drug's market entry and is expected to significantly enhance Regeneron's competitive position.
- European Market Outlook: The European Medicines Agency has accepted the marketing authorization application for cemdisiran, with final approval from the European Commission anticipated in H2 2027, laying the groundwork for Regeneron's expansion in the European market.
- Clinical Trial Results: Based on 24-week data, Regeneron announced in August that the treatment arm testing cemdisiran as a single agent in adults with symptomatic myasthenia gravis met the primary goals of the NIMBLE trial, further validating the drug's efficacy and safety.
See More
Dyne Therapeutics Appoints Barry Greene to Board of Directors
- New Board Appointment: Dyne Therapeutics has appointed Barry Greene to its Board of Directors, bringing over 30 years of biopharmaceutical experience focused on the development and commercialization of therapies for rare diseases, neuroscience, and oncology, which is expected to provide strategic guidance for the company.
- Rich Leadership Experience: Greene currently serves as the lead independent director at Karyopharm Therapeutics and has been on the Board since 2013, and his extensive leadership experience will aid Dyne in navigating the complex biopharmaceutical market.
- Former CEO Background: Greene previously held the position of CEO at Sage Therapeutics from December 2020 to July 2025, and his expertise in drug development and commercialization will support Dyne's future growth initiatives.
- Positive Stock Performance: Dyne shares closed at $20.87 on Monday, reflecting a 5.40% increase, indicating a positive market reaction to the new appointment, which may enhance investor confidence and drive future growth.
See More
Alnylam to Host 10th RNAi Roundtable Series
- RNAi Roundtable Series: Alnylam Pharmaceuticals announced its plan to host the 10th series of 'RNAi Roundtable' webinars in the coming months, featuring presentations from scientists and medical experts discussing recent advancements in the company's pipeline programs to address unmet clinical needs.
- Live Webcast Arrangement: Each event will be webcast live on the company's investor website, with replays available approximately three hours after each session, ensuring timely access to critical information for investors.
- 2030 Strategic Goals: Alnylam aims to increase its clinical programs from over 25 to more than 40 by 2030, demonstrating its commitment to sustainable innovation and market expansion in the RNAi therapeutics sector.
- Increased R&D Investment: The company is significantly ramping up its R&D investments to extend the application of RNAi technology, aiming to deliver multiple new transformative medicines for patients with serious diseases, thereby reinforcing its market leadership position.
See More
Alnylam Pharmaceuticals Shares Drop 24%, Yet Optimism Persists
- Significant Revenue Growth: Alnylam Pharmaceuticals reported a 121% year-over-year surge in product revenue to $1.04 billion in Q1, primarily driven by a 153% increase in its ATTR franchise, indicating strong market demand in the rare disease treatment sector.
- Profitability Improvement: The company achieved earnings per share (EPS) of $1.51, a substantial turnaround from a loss of $0.14 per share in the same period last year, demonstrating Alnylam's rapid transition into a profitable commercial powerhouse, which boosts investor confidence.
- Expansion into New Indications: New data for Alnylam's Amvuttra reinforces its position as a first-line treatment for cardiomyopathy, setting the stage for a massive commercial launch and further market share expansion.
- Strong Technological Moat: Alnylam's RNA interference platform creates a deep technological moat, and its collaboration with Inceptive Nucleics on AI accelerates the discovery of next-generation RNAi structures, ensuring its competitive edge in the biotech industry.
See More
Alnylam Pharmaceuticals Reports Strong Q1 Performance
- Significant Revenue Growth: Alnylam Pharmaceuticals reported a 121% year-over-year surge in product revenue to $1.04 billion in Q1, primarily driven by a 153% increase in its transthyretin amyloidosis (ATTR) franchise, indicating strong market demand in the rare disease treatment sector.
- Profitability Improvement: The company achieved earnings per share (EPS) of $1.51, a substantial turnaround from a loss of $0.14 per share in the same period last year, marking a significant improvement in profitability and showcasing its transition from a high-burn clinical biotech to a profitable commercial powerhouse.
- Broad Market Outlook: Alnylam's guidance for full-year 2026 net product revenue ranges between $4.9 billion and $5.3 billion, reflecting a 71% year-over-year growth at the midpoint, highlighting the company's potential to penetrate mainstream high-volume therapeutic markets, particularly in cardiomyopathy and hypertension.
- Strong Technological Moat: Alnylam's RNA interference (RNAi) drug delivery system creates a deep technological moat, and its strategic AI collaboration with Inceptive Nucleics accelerates the discovery of next-generation RNAi structures, ensuring the company's competitive edge in the rapidly evolving biotech landscape.
See More
Komodo Expands Partnership with Alnylam to Enhance AI Decision-Making
- Partnership Expansion: Komodo Health has expanded its strategic partnership with Alnylam Pharmaceuticals to scale the Marmot analytics platform across key enterprise functions, enhancing AI-driven decision-making and improving overall operational efficiency.
- Real-Time Intelligence Transformation: The Marmot platform, built on the Healthcare Map, integrates over 330 million de-identified patient journeys, enabling Alnylam to break free from fragmented analytics and achieve real-time, transparent healthcare intelligence, significantly reducing reporting cycles from months to hours.
- New Feature Launch: Komodo has released new capabilities for Marmot aimed at making healthcare intelligence accessible to all users, ensuring that every analysis is reproducible and verifiable, thereby enhancing the scientific rigor and accuracy of decision-making while embedding AI into core enterprise processes.
- Industry Transformation Trend: This partnership reflects a broader shift in healthcare and life sciences, as organizations move beyond mere AI experimentation to adopt new operating models centered around real-time intelligence, addressing increasingly complex market demands.
See More
Regeneron's Cemdisiran Marketing Applications Accepted by U.S. and European Regulators
- Drug Application Progress: Regeneron (REGN) and Alnylam Pharmaceuticals (ALNY) have had their marketing applications for the experimental therapy cemdisiran accepted by U.S. and European regulators, marking a significant advancement in treating myasthenia gravis.
- Priority Review Approval: The U.S. FDA has issued a priority review for cemdisiran's New Drug Application with a target action date in November, which will expedite the drug's market entry and is expected to significantly enhance Regeneron's competitive position.
- European Market Outlook: The European Medicines Agency has accepted the marketing authorization application for cemdisiran, with final approval from the European Commission anticipated in H2 2027, laying the groundwork for Regeneron's expansion in the European market.
- Clinical Trial Results: Based on 24-week data, Regeneron announced in August that the treatment arm testing cemdisiran as a single agent in adults with symptomatic myasthenia gravis met the primary goals of the NIMBLE trial, further validating the drug's efficacy and safety.
See More
Dyne Therapeutics Appoints Barry Greene to Board of Directors
- New Board Appointment: Dyne Therapeutics has appointed Barry Greene to its Board of Directors, bringing over 30 years of biopharmaceutical experience focused on the development and commercialization of therapies for rare diseases, neuroscience, and oncology, which is expected to provide strategic guidance for the company.
- Rich Leadership Experience: Greene currently serves as the lead independent director at Karyopharm Therapeutics and has been on the Board since 2013, and his extensive leadership experience will aid Dyne in navigating the complex biopharmaceutical market.
- Former CEO Background: Greene previously held the position of CEO at Sage Therapeutics from December 2020 to July 2025, and his expertise in drug development and commercialization will support Dyne's future growth initiatives.
- Positive Stock Performance: Dyne shares closed at $20.87 on Monday, reflecting a 5.40% increase, indicating a positive market reaction to the new appointment, which may enhance investor confidence and drive future growth.
See More
Alnylam to Host 10th RNAi Roundtable Series
- RNAi Roundtable Series: Alnylam Pharmaceuticals announced its plan to host the 10th series of 'RNAi Roundtable' webinars in the coming months, featuring presentations from scientists and medical experts discussing recent advancements in the company's pipeline programs to address unmet clinical needs.
- Live Webcast Arrangement: Each event will be webcast live on the company's investor website, with replays available approximately three hours after each session, ensuring timely access to critical information for investors.
- 2030 Strategic Goals: Alnylam aims to increase its clinical programs from over 25 to more than 40 by 2030, demonstrating its commitment to sustainable innovation and market expansion in the RNAi therapeutics sector.
- Increased R&D Investment: The company is significantly ramping up its R&D investments to extend the application of RNAi technology, aiming to deliver multiple new transformative medicines for patients with serious diseases, thereby reinforcing its market leadership position.
See More
