Arbutus Biopharma
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Arbutus Biopharma (ABUS) investor relations material

Arbutus Biopharma Q3 2025 earnings summary

Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.
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Q3 2025 earnings summary13 Nov, 2025

Executive summary

  • Focused on developing imdusiran (AB-729) and AB-101 for chronic hepatitis B, with a streamlined organization and reduced workforce to prioritize clinical development and cost management.

  • Ended strategic partnership with Qilu, regaining global rights to imdusiran and recognizing all previously deferred revenue.

  • Imdusiran (AB-729) clinical data showed 46% of Phase 2a patients met criteria to discontinue all treatment, with 94% of long-term follow-up patients remaining off all treatment for up to 2+ years.

  • Ongoing patent litigation against Moderna and Pfizer/BioNTech for use of LNP technology, with favorable claim construction rulings and trial dates set for 2026 and 2027.

  • Launched a new Scientific Advisory Board to guide clinical strategy.

Financial highlights

  • Total revenue for Q3 2025 was $0.5M, down from $1.3M in Q3 2024; nine-month revenue rose to $13.0M from $4.6M year-over-year, mainly due to $9.6M deferred revenue recognized after Qilu agreement termination.

  • Net loss for Q3 2025 was $7.7M ($0.04 per share), improved from $19.7M ($0.10 per share) in Q3 2024; nine-month net loss was $29.7M, down from $57.4M year-over-year.

  • Operating expenses for Q3 2025 were $9.2M, down from $22.8M in Q3 2024; nine-month operating expenses were $45.9M, down from $67.0M year-over-year.

  • Research and development expenses decreased to $5.8M from $14.3M year-over-year, and general and administrative expenses fell to $3.0M from $4.5M.

  • Cash, cash equivalents, and marketable securities totaled $93.7M as of September 30, 2025, with no outstanding debt.

Outlook and guidance

  • Expects significantly reduced net cash burn in 2025 compared to 2024 due to organizational changes and cost management.

  • All remaining restructuring-related payments are expected to be completed by Q1 2026.

  • Believes current cash resources are sufficient to fund operations for at least the next 12 months.

  • The company remains dedicated to accelerating the development and potential approval of imdusiran.

Impact of favorable Pfizer claim ruling
Imdusiran long-term off-treatment durability impact
Estimate cash runway given burn and cost cuts
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