Arbutus Biopharma Corporation (ABUS) SEC Filings & Earnings Calls
EquiReason read 25 Arbutus Biopharma Corporation SEC filings in the last 12 months. Latest: 8-K on 2026-10-22 — FDA lifted clinical hold on IND for AB-101, an oral PD-L1 inhibitor, enabling clinical development to resume..
Source: SEC EDGAR filings · figures as of 2026-06-30 · read by EquiReason
- Market cap
- 831.0M
- P/E TTM
- 5.3
- Dividend yield
- —
- 52-week
- —
- Next earnings
- 11 Nov, in 18 days
Every filing, read
last 12 months · SECWhat happened, the numbers inside, guidance and risks. The original is one click away.
22 Oct 20268-K · 8.01FDA lifted clinical hold on IND for AB-101, an oral PD-L1 inhibitor, enabling clinical development to resume.open
Risks flagged
Clinical hold removal reduces regulatory risk but does not guarantee clinical success or commercial viability.
“Clinical hold lifted, but AB-101 still requires clinical trial execution and eventual approval.”
5 Oct 2026SC 13D/ARoivant Sciences maintains 19.5% passive stake in Arbutus Biopharma after participating in a tender offer to keep proportionate ownership.open
Figures in the filing · each found in the filing text
| common_outstanding_shares · 2026-10-01 | 153,275,907 | |
| beneficial_ownership_percent · 2026-10-01 | 19.5% |
21 Aug 20268-K · 8.01Arbutus Biopharma announces modified Dutch auction tender offer to purchase up to $230M of common shares at $5.00-$5.75 per share.open
Figures in the filing · each found in the filing text
| tender offer value · Q3-2026 | $230M | |
| tender offer price range low · Q3-2026 | $5.00 | |
| tender offer price range high · Q3-2026 | $5.75 |
Risks flagged
Execution risk: tender offer not yet commenced and may not occur on described terms or at all.
“there can be no assurances that the Company will commence the tender offer on the terms described herein or at all” · word for word
12 Aug 202610-QArbutus received $178.4M from Moderna settlement, FDA granted Fast Track for imdusiran, and company evaluates return of capital to shareholders.open
Figures in the filing · each found in the filing text
| Noncontingent Settlement Payment Received · 2026-07-08 | $178M | |
| Contingent Settlement Payment Potential · unknown | $1.30B | |
| Genevant Ownership · 2026-06-30 | 16.0% | |
| Functional Cure Patients · unknown | 10 | |
| Phase 2a Patients Achieving Functional Cure or Off NA Therapy · unknown | 49 |
Risks flagged
European Patent Revocation
“On January 15, 2026, in a verbal decision, the Board of Appeal of the EPO revoked the '254 Patent.” · word for word
Contingent Payment Uncertainty
“Moderna is obligated to pay us and Genevant an additional aggregate contingent lump sum payment of $1.3 billion... upon a ruling that is favorable to us and Genevant in a limited appeal.” · word for word
Clinical Trial Risk
“We are currently developing imdusiran... for the treatment of chronic hepatitis B (cHBV).”
12 Aug 20268-K · 2.02Cash, cash equivalents and marketable securities $93M; Total revenue $1M (-91% y/y); Research and development expenses $3Mearningsopen
Figures in the filing · each found in the filing text
| Cash, cash equivalents and marketable securities · Q2-2026 | $93M | |
| Total revenue · Q2-2026 | $1M | -91% y/y |
| Research and development expenses · Q2-2026 | $3M |
Risks flagged
Revenue decline due to conclusion of Qilu partnership; reliance on settlement proceeds for capital return.
“Revenue decreased $9.7M due to recognizing all deferred revenue in prior year period upon partnership conclusion.”
16 Jul 20268-K · 1.02, 5.02, 8.01Noncontingent Settlement Payment (total) $950M; Arbutus share of Noncontingent Settlement Payment $178M; Contingent Settlement Payment (maximum) $1.30Bopen
Figures in the filing · each found in the filing text
| Noncontingent Settlement Payment (total) | $950M | |
| Arbutus share of Noncontingent Settlement Payment | $178M | |
| Contingent Settlement Payment (maximum) | $1.30B | |
| Termination fee | $1M | |
| Share repurchase authorization | $230M |
Risks flagged
Contingent payment of up to $1.3B depends on appellate ruling, which may not occur.
“Moderna is obligated to make an additional contingent lump sum payment of up to an aggregate $1.3 billion if certain events occur” · word for word
27 May 20268-K · 5.02, 5.07Shares authorized under 2026 Plan 16,300,000open
Figures in the filing · each found in the filing text
| Shares authorized under 2026 Plan | 16,300,000 |
13 May 20268-K · 2.02Total revenue $179M (+10055% y/y); License revenue from Genevant $179M; Net income $170Mearningsopen
Figures in the filing · each found in the filing text
| Total revenue · Q1-2026 | $179M | +10055% y/y |
| License revenue from Genevant · Q1-2026 | $179M | |
| Net income · Q1-2026 | $170M | |
| Net income per share (basic) · Q1-2026 | $0.88 | |
| Net income per share (diluted) · Q1-2026 | $0.87 | |
| Cash, cash equivalents and marketable securities · Q1-2026 | $95M | |
| Research and development expenses · Q1-2026 | $4M | -54% y/y |
| General and administrative expenses · Q1-2026 | $6M | +1% y/y |
| Common shares outstanding · Q1-2026 | 196,900,000 | |
| Weighted average shares (basic) · Q1-2026 | 193,768,641 |
Risks flagged
Revenue and profitability heavily dependent on one-time litigation settlement; core business remains clinical-stage with no approved products.
“Total revenue of $179.1M includes estimated license revenue from Genevant related to litigation settlement with Moderna” · word for word
13 May 202610-QNoncontingent Settlement Payment $950M; Contingent Settlement Payment $1.30B; Estimated Arbutus Share of Settlement $179Mopen
Figures in the filing · each found in the filing text
| Noncontingent Settlement Payment · 2026-07-08 | $950M | |
| Contingent Settlement Payment · unknown | $1.30B | |
| Estimated Arbutus Share of Settlement · 2026-07-08 | $179M | |
| Functional Cure Patients · Q1-2026 | 10 | |
| Phase 2a Patients Achieving Functional Cure or Off NA Therapy · Q1-2026 | 49 | |
| Ownership in Genevant · 2026-03-31 | 16.0% |
Risks flagged
Contingent Payment Risk
“In addition, Moderna is obligated to pay us and Genevant an additional aggregate contingent lump sum payment of $1.3 billion (the Contingent Settlement Payment) upon a ruling that is favorable to us and Genevant in a limited appeal... Under certain circumstances... if the Arbutus/Genevant §1498 Victory is subsequently overturned in Moderna’s favor in a final” · word for word
Pfizer/BioNTech Litigation Outcome Risk
“We continue to protect and defend our intellectual property, which is the subject of our ongoing lawsuit against Pfizer Inc. and BioNTech SE (collectively, Pfizer/BioNTech) for their use of our patented lipid nanoparticle (LNP) technology in their COVID-19 messenger ribonucleic acid interference (mRNA)-LNP vaccines.” · word for word
Clinical Trial Risk
“Our strategy, future operations, preclinical studies, clinical trials, and prospects; ... the potential for our product candidates to achieve their desired or anticipated outcomes;” · word for word
28 Apr 2026SC 13D/AWhitefort Capital reports 8.0% active stake in Arbutus Biopharma, with additional swap exposure.open
Figures in the filing · each found in the filing text
| Whitefort Capital beneficial ownership · 2026-04-24 | 8.0% | |
| Whitefort Capital total economic exposure · 2026-04-24 | 9.8% |
28 Apr 2026SC 13D/AWhitefort Capital reports 8.0% active stake in Arbutus Biopharma, with additional swap exposure.open
Figures in the filing · each found in the filing text
| Whitefort Capital beneficial ownership · 2026-04-24 | 8.0% | |
| Whitefort Capital total economic exposure · 2026-04-24 | 9.8% |
15 Apr 20268-K · 8.01Disclosed a material event under other events (litigation, recall, contract loss, or major announcement); filed financial statements and exhibits with this reportopen
Risks flagged
Clinical and regulatory risks remain; Fast Track does not guarantee approval.
“Fast Track program is designed to facilitate development and expedite review, but does not ensure approval.” · word for word
13 Apr 2026SC 13D/AWhitefort Capital Master Fund disclosed an 8.1% passive stake in Arbutus Biopharma Corp, acquired with working capital.open
Figures in the filing · each found in the filing text
| Beneficial Ownership Percentage (Whitefort Master Fund) · 2026-04-10 | 8.1% | |
| Aggregate Purchase Price · 2026-04-10 | $42M |
13 Apr 2026SC 13D/AWhitefort Capital Master Fund disclosed an 8.1% passive stake in Arbutus Biopharma Corp, acquired with working capital.open
Figures in the filing · each found in the filing text
| Beneficial Ownership Percentage (Whitefort Master Fund) · 2026-04-10 | 8.1% | |
| Aggregate Purchase Price · 2026-04-10 | $42M |
23 Mar 202610-KNoncontingent Settlement Payment $950M; Contingent Settlement Payment $1.30B; Restructuring Charges $13Mopen
Figures in the filing · each found in the filing text
| Noncontingent Settlement Payment · FY2025 | $950M | |
| Contingent Settlement Payment · FY2025 | $1.30B | |
| Restructuring Charges · FY2025 | $13M | |
| Common Shares Outstanding · 2026-03-18 | 195,478,068 | |
| Functional Cure Rate (IM-PROVE I Cohort A1) · IM-PROVE I · FY2025 | 25.0% | |
| Functional Cure Rate (IM-PROVE I, HBsAg <1000 IU/mL) · IM-PROVE I · FY2025 | 50.0% | |
| Functional Cure Rate (IM-PROVE II with nivolumab, HBsAg <1000 IU/mL) · IM-PROVE II · FY2025 | 25.0% | |
| ONPATTRO Royalties Earned by OMERS · ONPATTRO · FY2025 | $27M | |
| Genevant Ownership · FY2025 | 16.0% |
Risks flagged
Clinical Hold on AB-101 IND
“It may take considerable time and expense to resolve the clinical hold that has been placed on our IND application of AB-101 by the FDA, and no assurance can be given that the FDA will remove the clinical hold.” · word for word
Patent Litigation Uncertainty
“We are involved in patent infringement lawsuits to protect and assert our intellectual property rights against large, well-capitalized companies and the United States, which requires that we continue to expend substantial resources, and we may not be successful in these proceedings.” · word for word
Contingent Settlement Payment Risk
“We face risks associated with the Contingent Settlement Payment under the Moderna Settlement Agreement.” · word for word
No Product Revenue
“We do not generate revenues from product sales and may never be profitable from operations.” · word for word
Dependence on Third-Party Manufacturers
“We rely exclusively on third parties to formulate and manufacture our product candidates, which exposes us to a number of risks that may delay development, regulatory approval and commercialization of our products.” · word for word
23 Mar 20268-K · 2.02Cash, Cash Equivalents and Investments $92M (-25% y/y); Revenue $14M (+127% y/y); Net Loss $-34M (-52% y/y)earningsopen
Figures in the filing · each found in the filing text
| Cash, Cash Equivalents and Investments · Q4-2025 | $92M | -25% y/y |
| Revenue · FY2025 | $14M | +127% y/y |
| Net Loss · FY2025 | $-34M | -52% y/y |
| Research and Development Expenses · FY2025 | $25M | -53% y/y |
| Common Shares Outstanding · Q4-2025 | 192,500,000 | |
| Noncontingent Settlement Payment · FY2026 | $950M |
Risks flagged
Contingent payment risk from Moderna settlement
“$1.3 billion contingent upon appellate ruling that Section 1498 does not bar claims”
Ongoing litigation with Pfizer/BioNTech
“On-going lawsuit against Pfizer/BioNTech for LNP technology infringement”
3 Mar 20268-K · 1.01, 8.01Arbutus/Genevant settled LNP patent litigation with Moderna for $950M noncontingent payment plus up to $1.3B contingent on appeal outcome. Arbutus receives 20% of proceeds after litigation costs.open
Figures in the filing · each found in the filing text
| noncontingent payment · Q1-2026 | $950M | |
| contingent payment · unknown | $1.30B |
Risks flagged
Contingent payment dependent on appeal outcome; potential repayment if overturned.
“if the Arbutus/Genevant § 1498 Victory is subsequently overturned... Arbutus/Genevant is required to return the Contingent Payment” · word for word
20 Feb 20268-K · 8.01Disclosed a material event under other events (litigation, recall, contract loss, or major announcement); filed financial statements and exhibits with this reportopen
Risks flagged
Litigation outcome uncertain; could result in significant damages or licensing revenue.
“Lawsuit seeks damages for patent infringement; court ruling on summary judgment could impact case trajectory.”
6 Feb 20268-K · 8.01Disclosed a material event under other events (litigation, recall, contract loss, or major announcement); filed financial statements and exhibits with this reportopen
Risks flagged
Litigation risk: Patent infringement case against Moderna; outcome uncertain; could result in significant damages or no recovery.
“Litigation filed; court ruling on motions; no final judgment.”
Financial risk: Company has limited revenue; litigation costs may be material.
“Known metrics show low revenue; litigation expenses not disclosed.”
16 Jan 20268-K · 8.01Disclosed a material event under other events (litigation, recall, contract loss, or major announcement); filed financial statements and exhibits with this reportopen
Risks flagged
Patent litigation risk: revocation of European patent may reduce potential damages or settlement value in European cases; appeal uncertain.
“Decision likely to affect case against Moderna in Switzerland and one UPC case; written decision expected in months.”
11 Dec 20258-K · 8.01Disclosed a material event under other events (litigation, recall, contract loss, or major announcement); filed financial statements and exhibits with this reportopen
Risks flagged
Litigation outcomes are uncertain; legal costs and potential adverse rulings could impact financials.
“Forward-looking statements caution about uncertainties in patent litigation.”
13 Nov 20258-K · 2.02, 8.01Cash, Cash Equivalents and Investments $94M; Revenue $500,000.00 (-62% y/y); Research and Development Expenses $6M (-59% y/y)earningsopen
Figures in the filing · each found in the filing text
| Cash, Cash Equivalents and Investments · Q3-2025 | $94M | |
| Revenue · Q3-2025 | $500000.00 | -62% y/y |
| Research and Development Expenses · Q3-2025 | $6M | -59% y/y |
| Operating Cash Flow (9 months) · 9M-2025 | $-35M |
Risks flagged
Litigation outcomes uncertain; Moderna trial in 2026, Pfizer claim construction favorable but not final.
“Moderna litigation U.S. trial scheduled for March 2026; Pfizer claim construction ruling in September 2025” · word for word
Cash burn continues with no near-term revenue catalyst; reliance on litigation or partnership.
“Cash $93.7M, down from $122.6M; operating cash use $35M in 9 months”
13 Nov 202510-QFunctional cure rate (HBeAg negative, baseline HBsAg<1000 IU/mL) 50; overall functional cure rate (IM-PROVE I Cohort A1) 25; functional cure rate (IM-PROVE II nivolumab cohort, baseline HBsAg<1000 IU/mL) 25open
Figures in the filing · each found in the filing text
| functional cure rate (HBeAg negative, baseline HBsAg<1000 IU/mL) · IM-PROVE I Cohort A1 · 2024-11 | 50.0% | |
| overall functional cure rate (IM-PROVE I Cohort A1) · IM-PROVE I Cohort A1 · 2024-11 | 25.0% | |
| functional cure rate (IM-PROVE II nivolumab cohort, baseline HBsAg<1000 IU/mL) · IM-PROVE II nivolumab cohort · 2025-05 | 25.0% | |
| patients achieving functional cure or remaining off NA therapy (Phase 2a total) · Phase 2a total · 2025-09-30 | 48 | |
| patients remaining off NA therapy in long-term follow-up · long-term follow-up · 2025-09-30 | 94.0% | |
| AB-101 receptor occupancy at 40mg (healthy subjects) · Phase 1a/1b Parts 1&2 · 2025-09-30 | 100.0% | |
| AB-101 receptor occupancy at 30mg (cHBV patients) · Phase 1a/1b Part 3 · 2025-11 | 100.0% | |
| restructuring charge · corporate · Q1-2025 | $12M | |
| workforce reduction · corporate · Q1-2025 | 57.0% | |
| royalties earned by OMERS from ONPATTRO · LNP royalty · 2019-01-01 to 20 | $26M |
Risks flagged
Patent litigation outcome uncertainty
“We cannot assure you that we will be successful in our patent infringement lawsuits against Moderna and Pfizer/BioNTech.”
Clinical trial failure risk
“Our product candidates may not achieve their desired or anticipated outcomes.”
Cash burn and financing risk
“We may need additional financing to fund our operations.”
Dependence on single product candidate
“Our business is highly dependent on the success of imdusiran.”
Regulatory approval risk
“We may not obtain necessary regulatory approvals.”
Arbutus Biopharma Corporation — questions
- What did Arbutus Biopharma Corporation file recently?
- 25 SEC filings in the last 12 months. Latest: 8-K on 2026-10-22 — FDA lifted clinical hold on IND for AB-101, an oral PD-L1 inhibitor, enabling clinical development to resume.
Every figure on this page comes from Arbutus Biopharma Corporation's own SEC filings — see them on SEC EDGAR. Price data is licensed and shown only inside the product.
How these figures are read: methodology · EquiReason.