ABUS on Nasdaq

Arbutus Biopharma

Logo: https://www.arbutusbio.com/, Non-free logo, via Wikipedia5

Canadian Bio Tech Company

Arbutus Biopharma Corporation is a publicly traded Canadian (NASDAQ: ABUS) biopharmaceutical company with an expertise in liposomal drug delivery and RNA interference, and is developing drugs for hepatitis B infection. It is headquartered in Warminster, Pennsylvania.3 From Wikipedia, CC BY-SA 4.0

$4.29 up 0.10 (2.27%)Price as of Oct 15, 2026 at 17:33 UTC

Last updated Oct 16, 2026.

Overview

2007Founded1

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  • TickerABUS on Nasdaq1
  • Industrypharmaceutical industry1
  • HeadquartersBurnaby1
  • Websitearbutusbio.com
  • Incorporated inBritish Columbia, Canada6
  • Business address701 Veterans Circle, Warminster, Pa 189746
  • Filer categoryNon-accelerated filer, Smaller reporting company6

Arbutus Biopharma Corporation is a publicly traded Canadian (NASDAQ: ABUS) biopharmaceutical company with an expertise in liposomal drug delivery and RNA interference, and is developing drugs for hepatitis B infection.3

Financials

From the company’s reports to the SEC. Every number links to the filing it came from.

Key numbers, fiscal 2025

-271.0%Operating margin8
-237.9%Net margin8
128.2%Revenue growth, 20258
-43.7%Return on equity8
0.00×Debt to equity8
-$39.6MFree cash flow8

What sells

Revenue by product, business segment and region, as the company reports it to the SEC.

Products and services

Collaboration And Contracts brought in 89% of the revenue Arbutus Biopharma broke down this way in fiscal 2025.

  1. Collaboration And Contracts$12.6M889%up 222% from 2024
  2. Non-Cash Royalty$1.5M811%down 34% from 2024
Products and services by year
Products and services20242025
Collaboration And Contracts$3.9M$12.6M
Non-Cash Royalty$2.3M$1.5M

Where the money goes

Where each dollar of revenue went, fiscal 2025

  • Research and development100¢$25.2M

Out of $14.1M in revenue.8 The company lost money this year.

Financial statements

Revenue9101112138$14.1M in 2025+134% since 2019
0$10.0M$20.0M$30.0M$40.0M2019: $6.0M$6.0M20192020: $6.9M$6.9M2020+15%2021: $11.0M$11.0M2021+59%2022: $39.0M$39.0M2022+255%2023: $18.1M$18.1M2023−54%2024: $6.2M$6.2M2024−66%2025: $14.1M$14.1M2025+128%
Operating income9101112138-$38.2M in 2025−73% since 2019
-$150.0M-$100.0M-$50.0M02019: -$143.9M-$143.9M20192020: -$57.8M-$57.8M2020−60%2021: -$73.5M-$73.5M2021+27%2022: -$65.5M-$65.5M2022−11%2023: -$78.1M-$78.1M2023+19%2024: -$76.3M-$76.3M2024−2%2025: -$38.2M-$38.2M2025−50%
Net income9101112138-$33.5M in 2025−78% since 2019
-$200.0M-$150.0M-$100.0M-$50.0M02019: -$153.7M-$153.7M20192020: -$63.7M-$63.7M2020−59%2021: -$76.2M-$76.2M2021+20%2022: -$69.5M-$69.5M2022−9%2023: -$72.8M-$72.8M2023+5%2024: -$69.9M-$69.9M2024−4%2025: -$33.5M-$33.5M2025−52%

Every line of the income statement in the latest annual report, as filed.8

Period ending2025-12-312024-12-31
Revenue$14.1M$6.2M
Research and development$25.2M$54.0M
General and administrative$15.9M$22.1M
Change in fair value of contingent consideration-$1.8M$2.6M
Restructuring costs$12.9M$3.7M
Total operating expenses$52.2M$82.5M
Loss from operations-$38.2M-$76.3M
Interest income$4.1M$6.6M
Gain on sale of property and equipment$674.0K$0
Interest expense-$97.0K-$137.0K
Foreign exchange gain / (loss)$14.0K-$49.0K
Total other income$4.7M$6.4M
Net loss-$33.5M-$69.9M
Basic (in USD per share)-$0.17-$0.38
Diluted (in USD per share)-$0.17-$0.38
Basic (in shares)191.6M shares185.6M shares
Diluted (in shares)191.6M shares185.6M shares
Unrealized gain on available-for-sale securities$37.0K$286.0K
Comprehensive loss-$33.5M-$69.6M

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The story

Tekmira, as the company was formerly called, was formed as a wholly owned subsidiary of Inex Pharmaceuticals in 2005 after that company began collapsing after its regulatory and partnering strategy failed in 2004. Tekmira was fully spun out in 2007 and Tekmira absorbed the assets of Inex, which had been founded in 1992.

Inex had been developing liposomal formulations of off-patent cancer drugs, and licensed them to Talon Pharmaceuticals in 2005; Talon was acquired by Spectrum Pharmaceuticals in 2013, and three former Inex/Tekmira products reached the market and began generating royalties for Tekmira: Marqibo (liposomal vincristine), Alocrest (liposomal vinorelbine) and Brakiva (liposomal topotecan).

Inex had also acquired licenses to intellectual property, as well as staff and manufacturing facilities, concerning RNAi technology from Lynx Therapeutics in 1998; this set of technologies became the focus for Tekmira and it initially sought to develop liposomally encapsulated RNAi drugs for a broad range of indications.

Tekmira also worked on providing liposomal delivery technology to other companies. In 2007 it signed a license agreement with Alnylam Pharmaceuticals so that Alnylam could use it to deliver its own RNAi drugs; that deal was expanded into a manufacturing agreement in 2009.

Most of those products not focused on viral diseases faltered, and Tekmira had only $6.3 million in cash when it filed suit against Alnylam in 2011 for breaching its contract and stealing trade secrets. The suit was settled in 2012, with Alnylam agreeing to pay Tekmira $65 million in termination fees, and the companies negotiated a new license agreement with lower milestones and royalties, which covers Alnylam's product patisiran.

Tekmira caught the world's attention and its stock rose dramatically during the 2013 West African Ebola virus epidemic due to its drug candidate for Ebola fever, TKM-Ebola. Tekmira was developing it under a $140 million US Department of Defense contract. While its stock was trading high in January 2015, it acquired OnCore BioPharma, a company focused on hepatitis B.

On December 19, 2014, Tekmira announced the appointment of former Bill & Melinda Gates Foundation CFO Richard Henriques to the company's board of directors. The company simultaneously announced the forthcoming departure of Ian MacLachlan as Executive Vice President and Chief Technical Officer.

Development of TKM-Ebola was terminated in mid June 2015 during a Phase II trial, for lack of efficacy.

Read the full text

The next month, Tekmira changed its name to Arbutus Biopharma and said that it would focus on drugs to treat hepatitis B.

In March 2017 Arbutus signed another license for its liposome delivery technology, this time with Alexion Pharmaceuticals, for delivery of an mRNA drug candidate. This license was terminated in July 2017, when Alexion discontinued preclinical programs outside its core complement franchise.

In 2019, Arbutus began a phase 1 clinical study using AB-506 to treat chronic hepatitis B. The company released preliminary data in July and stopped the trial in October after two patients developed acute hepatitis. Now AB-729 is paving the way for Arbutus, as they recently received the FDA go ahead to pursue phase 2 trials, after having their data voted best in ILC, 2021; after abandoning development of previous investigational agents. AB-836, Arbutus's next generation capsid inhibitor, has shown potential against mutants in its phase 1 trials.

In July 2019, Arbutus Biopharma announced the sale of part of its royalty interest on future global net sales of ONPATTRO, an RNA interference therapeutic currently sold by Alnylam Pharmaceuticals, to OMERS for $20 million.

COVID-19

On March 10, 2023, U.S. District Judge Mitchell Goldberg rejected a bid by Moderna to dismiss some of the patent infringement claims brought against the company by Arbutus and its partner, Genevant Sciences.

Moderna settled their lawsuit and will pay Arbutus $950 million upfront and an additional $1.3 billion contingent upon a favorable resolution of Moderna’s Section 1498 appeal.

From Wikipedia’s article on Arbutus Biopharma, shared under CC BY-SA 4.0.7

Former names

  • TEKMIRA PHARMACEUTICALS CORPJun 8, 2011 to Aug 3, 20156

Timeline

  1. Aug 3, 2015Went public Listed on NASDAQ1
  2. 2007Founded Founded1

Recent filings

  1. Oct 7, 20264
  2. Oct 7, 20264
  3. Oct 7, 20264
  4. Oct 7, 20264
  5. Oct 7, 2026SCHEDULE 13G/A
  6. Oct 5, 20264
  7. Oct 5, 2026SCHEDULE 13D/A
  8. Oct 1, 2026SC TO-I/A
  9. Sep 30, 2026SC TO-I/A
  10. Sep 23, 20264
  11. Sep 23, 20264
  12. Sep 23, 20264
  13. Sep 23, 20264
  14. Sep 4, 2026SCHEDULE 13G
  15. Aug 24, 2026SC TO-I

Every filing from the last three years, summarized. The full record is on SEC EDGAR.2