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VolitionRx Q3 revenue rises 157% to about $1.6M

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Sentiment and the balance of points

Rhea-AI Sentiment reads the wording of the document, how positive or negative its language is on a 1 to 5 scale. The balance of points shown with the takes weighs what the document actually discloses, so the two can disagree, for example when a trial that missed its main goal is described in upbeat language.

Form Type
8-K

Rhea-AI Filing Summary

VolitionRx Limited (VNRX) reported third-quarter 2026 revenue of approximately $1.6 million, up 157% from approximately $0.6 million a year earlier, reflecting increased recognition of deferred revenue. Operating expenses were 14% lower year over year; operating loss narrowed 35% to $3.3 million from $5.1 million. Net loss was $3.8 million, including $0.4 million of noncash convertible-note charges, versus $5.4 million.

Cash and cash equivalents totaled approximately $2.4 million as of September 30, 2026, versus $1.1 million as of December 31, 2025. Third-quarter receipts included approximately $5.2 million in net proceeds from the at-the-market facility; Volition prepaid in cash the outstanding balance of its $7.5 million convertible note.

Business updates included September participation in DETECSEPS, a French government-funded €6.3 million program evaluating the automated Nu.Q® NETs assay as the sole biomarker for early sepsis detection, and an October letter of intent with Missionpharma; initial efforts are expected to focus on neonatal sepsis triage and prognostication. Volition expects to submit Nu.Q® Lung Cancer for French reimbursement this quarter. Publication of the feline lymphoma study is anticipated this quarter; peer-reviewed evidence of clinical utility is a necessary condition for a $5 million milestone payment.

4 points · 1 major

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Rhea-AI gives every point it takes from this document a weight. Minor counts 1, Moderate 3 and Major 9, so one Major point outweighs several Minor ones. The bar adds up the weights on each side, and when neither side holds more than 65% of the total the balance reads Mixed.

It reads the document as published, with the same rules for every company, and it does not look at what the market expected or at how the stock traded, so a point can be objectively good on a day the stock falls.

Rhea-AI Sentiment measures something else, the tone of the wording.

0 major · 0 points

How the balance works

Positive

  • Major pointVolition prepaid its outstanding $7.5 million convertible note in cash. 1.2× market cap
  • Moderate pointThird-quarter revenue increased 157% to approximately $1.6 million.
  • Moderate pointOperating loss narrowed 35% to $3.3 million year over year.
  • Moderate pointNet loss was $3.8 million, compared with $5.4 million a year earlier.

Negative

  • None.

Filing Explained

Effective November 1, 2026, the CEO’s annual base salary is half its original level until a substantial licensing agreement is executed; the chair and board have also agreed to reduce cash fees by at least half, lowering leadership compensation costs as the changes take effect.

Revenue Approximately $1.6 million Third quarter 2026; up 157% from approximately $0.6 million in the third quarter of 2025.
Operating expenses 14% lower Third quarter 2026 compared with the same period in 2025.
Operating loss $3.3 million Third quarter 2026; 35% narrower than $5.1 million in the third quarter of 2025.
Net loss $3.8 million Third quarter 2026, compared with $5.4 million in the third quarter of 2025; includes $0.4 million in noncash convertible-note charges.
Cash and cash equivalents Approximately $2.4 million As of September 30, 2026, compared with $1.1 million as of December 31, 2025.
Net proceeds from at-the-market facility Approximately $5.2 million Included in receipts during the third quarter of 2026.
Convertible note prepaid $7.5 million Volition prepaid the outstanding balance in cash during the third quarter of 2026.
Feline assay milestone payment $5 million Peer-reviewed publication evidencing clinical utility is a necessary condition for the payment.
deferred revenue financial
"increased recognition of deferred revenue"
Cash a company has already received for goods or services it has promised but not yet delivered; it's recorded as a liability because the company still owes that product, service, or future revenue recognition. For investors, deferred revenue signals upcoming work or deliveries that will convert into reported sales over time and affects short-term obligations, cash flow quality, and how quickly a firm can grow recognized revenue—think of it like prepaid subscriptions or gift cards a business must honor later.
at-the-market facility financial
"net proceeds from the at-the-market facility"
An at-the-market facility is a standing arrangement that lets a publicly traded company sell new shares directly into the open market at whatever the current market price is, typically through an investment bank acting as a sales agent. For investors it matters because it provides the company with a flexible way to raise cash without a large, one-time share offering; however, selling additional shares can dilute existing ownership and, by increasing supply, may pressure the stock price like adding more tickets to a limited-seat event.
convertible note financial
"outstanding balance of its $7.5 million convertible note"
A convertible note is a type of loan that a company gets from investors, which can later be turned into company shares instead of being paid back in cash. It matters because it helps startups raise money quickly without setting a fixed value for the company right away, making it easier to grow and attract investors.
lateral flow medical
"rapid point-of-care finger-prick lateral flow prototype"
A lateral flow test is a small, disposable diagnostic device that detects the presence of a substance (like a virus protein or antibody) in a liquid sample by letting it flow across a paper strip with embedded reagents, similar to a home pregnancy test. Investors care because these tests are cheap, fast, and easy to scale and distribute, making them a major revenue source during health events, subject to regulatory approval, manufacturing capacity, and changing demand.
CE-marked regulatory
"CE-marked automated assay"
CE-marked indicates a product meets European Union requirements for safety, performance and legal compliance, allowing it to be sold across the European Economic Area. For investors, a CE mark is like a passport or safety stamp — it reduces regulatory and market-entry risk, can speed sales and adoption across many countries, and signals the maker completed required testing and documentation, which can affect revenue forecasts and valuation.
Minimal Residual Disease (MRD) medical
"Minimal Residual Disease (MRD) opportunities"
The presence of minimal residual disease (MRD) means a very small number of cancer cells remain in the body after treatment, too few to cause symptoms or show up on routine scans but detectable with sensitive tests. For investors it matters because MRD status is a strong early indicator of whether a patient is likely to relapse and is increasingly used as a trial endpoint and regulatory signal, affecting a therapy’s market prospects and valuation much like finding glowing embers after a fire signals risk of re-ignition.
Revenue Approximately $1.6 million Up 157% from approximately $0.6 million in the third quarter of 2025
Operating expenses 14% lower Compared with the same period in 2025
Operating loss $3.3 million 35% narrower than $5.1 million in the third quarter of 2025
Net loss $3.8 million Compared with $5.4 million in the third quarter of 2025
Cash and cash equivalents Approximately $2.4 million As of September 30, 2026; compared with $1.1 million as of December 31, 2025
Net proceeds from at-the-market facility Approximately $5.2 million Included in third-quarter receipts
Convertible note prepaid $7.5 million Outstanding balance prepaid in cash during the quarter

FAQ

AI-generated questions and answers. How Rhea-AI works. Not financial advice.

What were VNRX's third-quarter 2026 financial results?

Volition reported approximately $1.6 million in revenue, up 157% from approximately $0.6 million a year earlier. Operating loss was $3.3 million, compared with $5.1 million, and net loss was $3.8 million, compared with $5.4 million.

How much cash did VNRX report, and what convertible note did it repay?

Cash and cash equivalents were approximately $2.4 million as of September 30, 2026. Third-quarter receipts included approximately $5.2 million in net proceeds from the at-the-market facility, and Volition prepaid in cash the outstanding balance of its $7.5 million convertible note.

What does Volition's Missionpharma letter of intent cover?

Volition signed a letter of intent with Missionpharma in October. Initial efforts are expected to focus on triaging and prognostication for neonatal sepsis; Missionpharma serves more than 100 million patients annually as a healthcare-products distributor.

What is the expected use of Nu.Q Lung Cancer in France if reimbursement is achieved?

Volition currently expects to submit Nu.Q Lung Cancer for French reimbursement this quarter. It says achieving reimbursement would be a step toward routine clinical use in France before expansion to additional geographies.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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EXHIBIT 99.1

VolitionRx Limited Announces Third Quarter 2026 Financial Results and Business Update

 

Conference call to discuss financial and operational results scheduled for

 

Friday, November 13 at 8:30 a.m. U.S. Eastern Time

 

Henderson, Nevada, November 12, 2026 /PRNewswire/ -- VolitionRx Limited (NYSE AMERICAN: VNRX) (“Volition”), a multi-national epigenetics company, today announces financial results and a business update for the third quarter of 2026.Volition management will host a conference call tomorrow, November 13 at 8:30 a.m. U.S. Eastern Time/2:30 p.m. Central European Time to discuss these results. Conference call details can be found below.

 

Cameron Reynolds, President and Group Chief Executive Officer, said:

 

“It has been a very full quarter as we have continued to execute our plan to commercialize our game-changing Nu.Q® platform. We have made strong progress across our key product pillars this year, evidencing clinical utility across a broad spectrum of indications whilst driving commercialization and licensing efforts worldwide. At the same time, we have taken decisive action to strengthen our financial profile by cutting costs and significantly reducing convertible note debt.

 

“In our Nu.Q® NETs pillar, in September we participated in the launch of DETECSEPS, a French government-funded €6.3 million program evaluating our automated Nu.Q® NETs assay as the sole biomarker for early detection of sepsis in hospital emergency departments. In August, Critical Care Medicine published data showing Nu.Q® NETs H3.1 to be an independent predictor of 28-day mortality and need for renal replacement therapy in sepsis. Published clinical data indicate that Nu.Q® NETs distinguishes sepsis from non-infectious inflammation and provides strong prognostic value for organ failure and mortality.

 

“Furthermore, our rapid point-of-care finger-prick lateral flow prototype has demonstrated high correlation with our CE-marked automated assay in ICU sepsis patients. To accelerate commercialization and global market access, particularly in resource-constrained countries and humanitarian emergency settings, we signed in October a Letter of Intent with Missionpharma, a global distributor of healthcare products serving over 100 million patients annually. Initial efforts with Missionpharma are expected to focus on triaging and prognostication for neonatal sepsis. In parallel, our diagnostic collaborations with Sysmex Corporation and Werfen’s Immunoassay Technology Center continue to advance across NETs-related indications.

 

“In Nu.Q® Cancer, we are advancing toward our French reimbursement submission for Nu.Q® Lung Cancer with support from our long-term collaborators at Hospices Civils de Lyon in France. We currently expect to submit this quarter. Achieving reimbursement would be an important step on the path to routine clinical use in France before rolling out to additional geographies. For our novel Capture-Seq™ technology, following peer-reviewed publication of our clinical data in August, we are in active licensing discussions with several major liquid biopsy and diagnostic companies to target Multi-Cancer Early Detection (MCED) and Minimal Residual Disease (MRD) opportunities representing combined annualized addressable markets estimated at over $36 billion¹.

 

“In our Nu.Q® Vet pillar, our clinical manuscript, submitted for peer review in May, demonstrated that our feline prototype assay detected 86% of feline lymphomas at 97% specificity. We currently anticipate publication of this study this quarter. As a reminder, a peer reviewed publication evidencing clinical utility is a necessary condition to unlock a $5 million milestone payment. Commercialization of the assay could open a significant market among senior pet cats.

 

 

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“I am personally leading our most advanced partner negotiations and, to underline my commitment to closing them, have voluntarily agreed to a further reduction in my base salary, effective November 1, 2026, such that my annual base salary is now 50% of its original level, until execution of a substantial licensing agreement. Furthermore, the chairman and entire board of directors have also agreed to reduce their cash fees by at least 50%”.

 

Financial Highlights for the Third Quarter 2026

 

•

Revenue: Third quarter 2026 revenue was approximately $1.6 million, up 157% compared to $0.6 million in the third quarter of 2025, reflecting an increase in recognition of deferred revenue.

 

 

•

Operating Expenses: Operating expenses for the third quarter of 2026 were 14% lower than the same period in 2025, reflecting savings from Volition’s ongoing cost-reduction program, including a 28% reduction in headcount compared to the same point last year.

 

 

•

Operating Loss: Operating loss for the third quarter of 2026 narrowed to $3.3 million, a 35% improvement compared to $5.1 million in the third quarter of 2025.

 

 

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Net Loss: Net loss for the third quarter of 2026 was $3.8 million, including non-cash charges of $0.4 million related to convertible notes, compared to a net loss of $5.4 million in the prior-year period.

 

 

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Balance Sheet & Debt Reduction: Cash and cash equivalents totaled approximately $2.4 million as of September 30, 2026, compared to $1.1 million as of December 31, 2025. Receipts in the third quarter included approximately $5.2 million in net proceeds from Volition’s at-the-market facility. During the third quarter, Volition prepaid in cash the outstanding balance of its$7.5 million convertible note.

 

Event: VolitionRx Limited Third Quarter 2026 Earnings and Business Update Conference Call

Date: Friday, November 13, 2026

Time: 8:30 a.m. U.S. Eastern Time/2:30 p.m. Central European Time

 

U.S. & Canada Dial-in: 1-877-407-9716 (toll free)

U.K. Dial-in: 0 800 756 3429 (toll free)

Toll/International: 1-201-493-6779

Conference ID: 13763536

 

Rodney Rootsaert, Corporate Secretary, VolitionRx will host the call along with Cameron Reynolds, President and Group Chief Executive Officer and Terig Hughes, Group Chief Financial Officer. The call will provide an update on important events that have taken place in the third quarter of 2026, subsequent events and upcoming milestones.

 

A live audio webcast of the conference call will also be available on this link. In addition, a telephone replay of the call will be available until November 27, 2026. The replay dial-in numbers are 1-844-512-2921 (toll-free) in the U.S. and Canada and 1-412-317-6671 (toll) internationally. Please use replay pin number13763536.

 

 

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Notes:

 

 

1.

Volition internal estimate based on VNRX TAM Model

 

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About Volition

 

Volition is a multi-national company focused on advancing the science of epigenetics. Volition is dedicated to saving lives and improving outcomes for people and animals with life-altering diseases through earlier detection, as well as disease and treatment monitoring.

 

Through its subsidiaries, Volition is developing and commercializing simple, easy to use, cost-effective blood tests to help detect and monitor a range of diseases, including some cancers and diseases associated with NETosis, such as sepsis. Early detection and monitoring have the potential not only to prolong the life of patients, but also to improve their quality of life.

 

The contents found at Volition’s website address, www.volition.com, are not incorporated by reference into this document and should not be considered part of this document. Such website address is included in this document as an inactive textual reference only.

 

Media Enquiries: Ellen Amonoo, Volition, mediarelations@volition.com

 

Safe Harbor Statement

 

Statements contained in this press release and made on the related conference call may be "forward-looking statements" within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. Forward-looking statements are those that are not statements of historical fact and instead address predictions, expectations, beliefs, plans, projections, objectives, goals, assumptions or future events or performance. Words such as "expects," "anticipates," "intends," "plans," "aims," "targets," "believes," "seeks," "estimates," "optimizing," "potential," "goal," "suggests," "continue," "project," "could," "would," "should," "may," "will" and similar expressions identify such statements.

 

These forward-looking statements relate to, among other topics, Volition's expectations regarding revenue opportunities and growth; the effectiveness and availability of its blood-based diagnostic, prognostic and disease monitoring tests; its ability to develop and successfully commercialize such test platforms for the early detection and monitoring of cancer and other diseases; its expectations regarding future publications and the related milestone payment; the timing and outcome of its reimbursement submission in France and the DETECSEPS program; estimates of addressable markets; its cost-reduction plans; its liquidity, capital needs and ability to fund operations; and its success in securing, and the terms of, licensing and/or distribution or other agreements with third parties, including a definitive agreement with Missionpharma.

 

Forward-looking statements are based on current expectations, estimates and projections about Volition's business, in part on assumptions made by management. They are not guarantees of future performance and involve risks and uncertainties that are difficult to predict and that could cause actual results to differ materially from those anticipated. These risks and uncertainties include, without limitation: Volition's need for additional financing, which may not be available on acceptable terms or at all, the uncertain timing of publication of Volition's feline lymphoma study; the timing and outcome of Volition's reimbursement submission in France and of the DETECSEPS program; Volition's dependence on key collaborators and distributors, including Sysmex Corporation, Werfen, Missionpharma and Hospices Civils de Lyon; the assumptions underlying Volition's addressable market estimates; the results of studies testing the efficacy of Volition's tests; failure to develop and commercialize its products, which may prevent it from executing its plan of operations; failure to obtain necessary regulatory clearances or approvals; failure to achieve healthcare system or insurance reimbursement; failure of the marketplace to accept its products; failure to secure adequate intellectual property protection; the highly competitive and rapidly evolving nature of the diagnostics and disease monitoring market, which may render its products obsolete; downturns in domestic and foreign economies; and other risks identified in Volition's most recent Annual Report on Form 10-K, its Quarterly Reports on Form 10-Q, and other documents filed with the Securities and Exchange Commission.

 

Forward-looking statements are made as of the date hereof and, except as required by law, Volition undertakes no obligation to update them to reflect future events or circumstances.

 

Nu.Q®, Nucleosomics™, Capture-PCR™, Capture-Seq™ and rNuQ™ and their respective logos are trademarks and/or service marks of VolitionRx Limited and its subsidiaries. All other trademarks, service marks and trade names referred to in this press release or associated video or link are the property of their respective owners. Additionally, unless otherwise specified, all references to “$” refer to the legal currency of the United States of America.

 

 

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