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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.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.
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