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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.
- Imdusiran advances, cost cuts, and strong cash extend runway into Q4 2026.ABUS
Q2 20242 Feb 2026 - Imdusiran achieved 33% functional cure in HBV phase IIa, with more data and milestones ahead.ABUS
Jefferies 2024 Global Healthcare Conference31 Jan 2026 - Imdusiran and novel immunotherapies show strong promise for hepatitis B functional cure.ABUS
H.C. Wainwright 26th Annual Global Investment Conference 202421 Jan 2026 - Imdusiran and AB-101 advance in HBV trials, backed by strong cash and global partnership strategy.ABUS
Baird's 2024 Global Healthcare Conference21 Jan 2026 - Phase 2a trials show strong surface antigen loss and high nucleoside discontinuation rates.ABUS
H.C. Wainwright 5th Annual Viral Hepatitis Virtual Conference19 Jan 2026 - Q3 2024 saw narrowed losses, pipeline progress, and a cash runway into Q4 2026.ABUS
Q3 202416 Jan 2026 - Phase II-A data show up to 50% hepatitis B cure; major legal and pipeline milestones ahead.ABUS
Jefferies London Healthcare Conference 202412 Jan 2026 - Imdusiran shows 50% functional cure in HBV, with phase 2b and strong financial runway ahead.ABUS
Status Update12 Jan 2026 - Up to $300M in securities, including $100M ATM shares, to fund HBV drug development and operations.ABUS
Registration Filing16 Dec 2025 - Virtual annual meeting to vote on directors, pay, auditor, with strong governance and oversight.ABUS
Proxy Filing2 Dec 2025
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