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Alnylam Pharmaceuticals, Inc. Q4 2025 Earnings Call Summary

2026-02-12 21:31
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Alnylam Pharmaceuticals, Inc. Q4 2025 Earnings Call Summary

Alnylam Pharmaceuticals, Inc. Q4 2025 Earnings Call Summary Moby Intelligence Fri, February 13, 2026 at 5:31 AM GMT+8 3 min read In this article: ALNY +1.92% Alnylam Pharmaceuticals, Inc. Q4 2025 Earn...

Alnylam Pharmaceuticals, Inc. Q4 2025 Earnings Call Summary Moby Intelligence Fri, February 13, 2026 at 5:31 AM GMT+8 3 min read In this article: Alnylam Pharmaceuticals, Inc. Q4 2025 Earnings Call Summary Alnylam Pharmaceuticals, Inc. Q4 2025 Earnings Call Summary - Moby

Strategic Performance and Platform Evolution

  • Achieved full-year GAAP profitability in 2025, a landmark transition driven by 81% year-over-year growth in net product revenues.

  • The TTR franchise delivered $858 million in Q4, representing 151% growth year-over-year, primarily fueled by the U.S. launch of Amvuttra for ATTR cardiomyopathy.

  • Amvuttra has approached parity with tafamidis in share of new treatment starts by its second full quarter post-launch, signaling a shift in prescribing dynamics.

  • Launched Cyrillis, a proprietary enzymatic ligation-based manufacturing platform designed to expand capacity and reduce cost of goods for RNAi therapeutics.

  • Management attributes commercial success to broad first-line payer access, with over 90% of payers providing coverage without step-through requirements.

  • The Alnylam 2030 strategy aims for a 25% revenue CAGR and 30% non-GAAP operating margins, leveraging a pipeline of over 25 clinical programs.

2026 Guidance and Long-term Strategic Goals

  • 2026 TTR revenue guidance of $4.4 billion to $4.7 billion assumes continued brisk category growth and a mid-single-digit net price decrease in the U.S.

  • Anticipate a Q1 2026 revenue headwind due to pricing alignment in Germany for the cardiomyopathy launch and annual U.S. insurance reauthorizations.

  • Expect to share clinical de-risking data in the second half of 2026 for Huntington’s disease (ALN-HTT02) and obesity (ACVR1C) programs.

  • The 2030 roadmap includes launching nuceresiran, which lacks royalty obligations and is expected to drive operating margins toward the mid-40s post-2030.

  • Planned R&D investment will remain at approximately 30% of revenues to accelerate organic innovation and selectively access external technologies.

Operational and Financial Risk Factors

  • Gross margin on product sales decreased to 77% in 2025 due to higher royalty tiers payable to Sanofi as Amvuttra revenues scaled.

  • International TTR revenue growth in 2026 is expected to be consistent with 2025, tempered by lower launch pricing for cardiomyopathy in European markets.

  • Collaboration revenue is projected to decline 38% in 2026 because a one-time $300 million milestone from the zalesiran program will not recur.

  • Management flagged potential near-term 'choppiness' in Q1 results due to fewer shipping weeks and seasonal insurance dynamics.

Q&A Session Insights

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Competitive dynamics and pricing sustainability through 2027
  • Management believes they are well-positioned to manage future competition due to established first-line access and a 25% CAGR goal that already accounts for market entrants.

  • Confirmed that value-based agreements have seen minimal utilization to date, supporting stable net pricing despite broader access.

Story Continues Go/no-go criteria for Huntington's disease Phase 3 trial
  • The primary focus for upcoming data is safety and achieving over 50% knockdown of the huntingtin protein without the NfL increases seen in rival programs.

  • Management expressed willingness to accelerate to Phase 3 based on strong target engagement and safety data even if functional clinical data is still preliminary.

Strategic rationale for ACVR1C over INHBE in obesity
  • ACVR1C was prioritized because internal genetics and preclinical models suggest it is a more potent target for weight loss without muscle loss.

  • The strategy focuses on unique patient segments and combinations that address gaps left by current GLP-1 therapies.

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