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VolitionRx Announces Data Showing the Prognostic Value of its Nu.Q® Cancer Test

(Very Positive)
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Volition (NYSE AMERICAN: VNRX) reported new clinical data on its Nu.Q® Cancer Assay in newly diagnosed non-small cell lung cancer. The study suggests prognostic value for overall and progression-free survival, and may help identify patients suitable for curative care. The paper is under peer review.

Clinical certification at Hospices Civils de Lyon is completed, and a reimbursement dossier is being prepared under France’s RIHN framework. Volition is in discussions with hospital networks and potential licensees and anticipates about €50 revenue per test in a direct sales model.

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Positive

  • Clinical study suggests Nu.Q® Cancer provides prognostic information in newly diagnosed lung cancer
  • Data indicate potential to better identify patients who may benefit from curative care
  • Clinical certification of Nu.Q® Cancer completed at Hospices Civils de Lyon
  • Reimbursement dossier preparation underway under France’s RIHN framework
  • Reimbursement eligibility decision expected within five months once dossier is admissible
  • Company anticipates approximately €50 revenue per Nu.Q® Cancer test in direct sales model

Negative

  • Nu.Q® Cancer test is not yet approved for routine clinical use
  • Clinical paper remains under peer review, so findings are not yet finalized
  • Reimbursement in France is not yet granted and remains subject to review
  • Commercial revenue from Nu.Q® Cancer depends on future adoption and reimbursement decisions

News Market Reaction – VNRX

+3.70%
9 alerts
+3.70% Session close to close
+6.4% Peak Tracked
-10.6% Trough Tracked
$16.69M Market Cap
0.8x Rel. Volume

In the Jul 7 session, VNRX gained 3.70%, reflecting a moderate positive market reaction. Argus tracked a peak move of +6.4% during that session. Argus tracked a trough of -10.6% from its starting point during tracking. Our momentum scanner triggered 9 alerts that day, indicating moderate trading interest and price volatility.

Data tracked by StockTitan Argus on the day of publication.

Market Context

New clinical data suggest Nu.Q Cancer may aid prognostication in newly diagnosed lung cancer, with F...
Analysis

New clinical data suggest Nu.Q Cancer may aid prognostication in newly diagnosed lung cancer, with French clinical certification completed and a reimbursement dossier planned, while investors must still weigh financing needs, resale overhang, and execution on commercialization.

Key Figures

Per-test revenue: €50 per test Reimbursement decision window: 5 months
2 metrics
Per-test revenue €50 per test Anticipated revenue to Volition for direct Nu.Q Cancer sales
Reimbursement decision window 5 months Maximum timeframe after dossier deemed admissible under RIHN framework

Historical Context

5 past events · Latest: Jun 17 (Positive)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Jun 17 collaboration deal Positive -2.1% Collaboration with Sysmex to optimize Nu.Q NETs assay on its platform.
Jun 07 public offering Negative -20.4% Dilutive equity and warrant financing raising $4.6M gross proceeds.
Jun 03 patent filing Positive -10.3% Patent application for Nu.Q NETs use in Ebola triage and monitoring.
May 27 business update Positive +0.0% Update on commercial momentum, multi-billion TAMs, and Q1 2026 revenue.
May 14 earnings report Neutral -9.1% Q1 2026 financials with higher revenue but continued losses and cash burn.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Recent VolitionRx announcements, including partnerships and financings, have more often been followed by negative next-day share moves.

Key Terms

h3k27me3-nucleosomes, epigenetic biomarkers, non small cell lung cancer, reimbursement dossier, +1 more
5 terms
h3k27me3-nucleosomes medical
"Prognostic value of circulating H3K27Me3-nucleosomes in newly diagnosed lung cancer"
H3K27me3-nucleosomes are units of DNA wrapped around protein spools where a specific chemical tag — three methyl groups added to the 27th spot on histone H3 — marks regions of the genome as “off.” Think of them as sticky notes placed on a book’s pages to keep certain chapters closed; they control which genes are silenced. Investors watch them because their patterns can be diagnostic biomarkers and drug targets for cancers and other diseases, influencing the commercial value of therapies and diagnostics.
epigenetic biomarkers medical
"The integration of epigenetic biomarkers, such as circulating H3K27Me3-nucleosome"
Epigenetic biomarkers are measurable chemical or molecular tags—such as DNA methylation patterns or histone changes—that affect whether genes are turned on or off without changing the underlying DNA code. They matter to investors because they can serve as signals for diagnosing diseases, predicting outcomes, monitoring treatment response, and guiding drug development and regulatory decisions; think of them as sticky notes on the genome that reveal which chapters are being read or skipped.
non small cell lung cancer medical
"at Non Small Cell Lung Cancer diagnosis, can provide valuable information"
A broad category of lung cancers that behave and are treated differently from the faster-spreading small cell type, encompassing several common tumor kinds such as adenocarcinoma and squamous cell carcinoma. Investors care because success or failure of diagnostics and treatments for this large patient group directly affects drug sales, clinical trial outcomes, regulatory approvals and healthcare spending — similar to how a dominant product segment drives an entire supplier market.
reimbursement dossier regulatory
"we are working towards the submission of our reimbursement dossier in the coming months"
A reimbursement dossier is a compiled package of scientific studies, clinical outcomes, cost-effectiveness analyses, pricing proposals and real-world use information that manufacturers submit to health insurers or government payers to request coverage and a reimbursement price for a drug, device or medical service. It matters to investors because successful dossiers influence whether and how widely a product will be paid for, which directly affects sales, market access and revenue potential — like a detailed sales pitch aimed at payers rather than patients.
innovative procedures outside the nomenclature regulatory
"under the framework of the "Innovative Procedures Outside the Nomenclature" (RIHN-"
Medical techniques or clinical services that are new, customized, or performed in ways not listed in the official coding or classification systems used for billing and regulation. For investors this matters because procedures outside the nomenclature can be harder to get reimbursed, more difficult to price and track, and often face greater regulatory scrutiny and adoption uncertainty — like selling a product that has no barcode, making revenue and demand harder to predict.

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

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HENDERSON, Nev., July 7, 2026 /PRNewswire/ -- VolitionRx Limited (NYSE AMERICAN: VNRX) ("Volition"), a multi-national epigenetics company, today announces the release of a new clinical study demonstrating the significant prognostic value of its Nu.Q® Cancer Assay in newly diagnosed lung cancer patients, which could help clinicians identify patients' likely outcomes and personalize treatment selection accordingly. The clinical paper entitled "Prognostic value of circulating H3K27Me3-nucleosomes in newly diagnosed lung cancer patients: Real-world evidence1" has been written in conjunction with researchers and clinicians at the Hospices Civils de Lyon (HCL), France's second largest university hospital system, and is currently under peer review.

Dr Andrew Retter, Medical Consultant, Volition said:

"Nu.Q® Cancer represents a significant advancement in lung cancer patient management, offering clinicians an additional tool to enhance precision in treatment selection and monitoring and is a test we envisage will be used routinely in the clinic once approved.

"We have worked closely with the Lyon team over several years to develop the strong scientific and clinical evidence to support the use of Nu.Q® in the management of cancer patients. These results indicate that measuring methylated nucleosome biomarker levels with the Nu.Q® test, at Non Small Cell Lung Cancer diagnosis, can provide valuable information about survival, progression-free survival and, crucially, enhance the identification of patients who may benefit from curative care1-4.

"The integration of epigenetic biomarkers, such as circulating H3K27Me3-nucleosome, into personalized medicine frameworks holds great promise for refining patient stratification and treatment selection.

The test is simple to complete and easy to implement, the new information helps to empower bedside clinicians and their patients to make better informed decisions on treatments and planning future care together."

Frederic Wuilque, Vice President, Global Products, added:

"The first step in introducing the Nu.Q® Cancer test into routine clinical practice, the clinical certification at HCL, has been completed.
"With the active support of HCL, we are working towards the submission of our reimbursement dossier in the coming months, under the framework of the "Innovative Procedures Outside the Nomenclature" (RIHN-référentiel des actes innovants hors nomenclature). Once the dossier is classified as admissible, we understand that determination of eligibility for reimbursement coverage is mandated to take no more than five months.
"We are delighted to showcase more evidence to demonstrate the clinical utility of our Nu.Q® Cancer test and would like to thank our long term collaborator, Hospices Civils de Lyon, for their continued support. We continue to move through the steps on the path to the first use of Nu.Q® in clinical practice, an exciting prospect which is core to Volition's mission, using our tests to help save lives."

Mr. Gael Forterre, Chief Commercial Officer, Volition concluded:

"From a commercial perspective, France is just the beginning: the Volition team is actively discussing Nu.Q® Cancer, not only with hospital networks in other countries but also potentially licensing the technology to third party collaborators. For this direct sales model we anticipate approximately €50 per test as revenue to Volition.
"Reimbursement will be a major milestone for Volition in the commercialization and licensing of Nu.Q® in the human cancer field. Once achieved, we anticipate the introduction into routine clinical use in France."

About the Study

A large, real-world evidence study which demonstrated that plasma levels of Nu.Q® Cancer assay H3K27Me3 were associated with cancer stage, and highly elevated levels were observed in patients with a poor outcome.
Overall survival (OS) analysis revealed that patients with a H3K27Me3-nucleosome level below the optimal cut-off had a significantly better mean survival compared to those with higher concentrations, particularly for patients who are ctDNA-negative and therefore lacking detectable actionable mutations.
Interestingly, a Cox Proportional Hazards (CPH) prognostic model, integrating baseline H3K27Me3-nucleosome concentrations with commonly collected clinical covariates (cancer stage, ctDNA molecular profile and age) enabled stratification of patients at diagnosis into low and high risk mortality groups, facilitating prediction of patient-level survival probabilities in a timeline of up to 30 months.

1. Kotronoulas A,et al. Prognostic value of circulating H3K27Me3-nucleosomes in newly diagnosed lung cancer patients: Real-world evidence
Grolleau E, et al. Circulating H3K27 Methylated Nucleosome Plasma Concentration: Synergistic Information with Circulating Tumor DNA Molecular Profiling. Biomolecules. 2023;13(8):1255. https://doi.org/10.3390/biom13081255
2
. Couraud S, et al  Baseline values of circulating nucleosomes in Lung Cancer: NUCLEO-LUNG study. ELCC 2024 Poster
3. Marie Piecyk et al, "H3K27Me3-nucleosome is a strong prognostic biomarker in Non-Small Cell Lung Cancer: interim results from the analysis of up to 832 patients at baseline" Poster 395 ELCC 2025
4. Global Cancer Observatory 2022 (accessed Jan 20, 2026)

About Reimbursement

The Innovative Procedures Outside the Nomenclature (RIHN-référentiel des actes innovants hors nomenclature) framework allows for the early and temporary support of innovative procedures. This support is contingent upon the collection of data to facilitate the subsequent evaluation of these procedures by the French National Authority for Health (HAS), with a view to their integration into standard practice. Established by the Direction General for Healthcare (DGOS) as part of the development of innovation in healthcare, the RIHN provides a long-term support mechanism for innovative medical biology and anatomical pathology.

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.

Volition's research and development activities are centered in Belgium, with an innovation laboratory and office in the U.S. and an office in London.  

The contents found at Volition's website address 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:

Louise Batchelor, Volition, mediarelations@volition.com,+44 (0)7557 774620

Safe Harbor Statement

Statements in this press release 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, that concern matters that involve risks and uncertainties that could cause actual results to differ materially from those anticipated or projected in the forward-looking statements. Words such as "expects," "anticipates," "intends," "plans," "aims," "targets," "believes," "seeks," "estimates," "optimizing," "potential," "goal," "suggests," "could," "would," "should," "may," "will" and similar expressions identify forward-looking statements. These forward-looking statements relate to, among other topics, Volition's expectations related to revenue opportunities and growth, the effectiveness and availability of Volition's blood-based diagnostic, prognostic and disease monitoring tests, Volition's ability to develop and successfully commercialize such test platforms for early detection of cancer and other diseases as well as serving as a diagnostic, prognostic or disease monitoring tools for such diseases, Volition's expectations regarding future publications, Volition's success in securing licensing and/or distribution agreements with third parties for its products, and Volition's expectations regarding the terms of such agreements. Volition's actual results may differ materially from those indicated in these forward-looking statements due to numerous risks and uncertainties, including, without limitation, results of studies testing the efficacy of its tests. For instance, if Volition fails to develop and commercialize diagnostic, prognostic or disease monitoring products, it may be unable to execute its plan of operations. Other risks and uncertainties include Volition's failure to obtain necessary regulatory clearances or approvals to distribute and market future products; Volition's failure to achieve healthcare system or insurance plan reimbursement for its products; a failure by the marketplace to accept the products in Volition's development pipeline or any other diagnostic, prognostic or disease monitoring products Volition might develop; Volition's failure to secure adequate intellectual property protection; Volition will face fierce competition and Volition's intended products may become obsolete due to the highly competitive nature of the diagnostics and disease monitoring market and its rapid technological change; downturns in domestic and foreign economies; and other risks, including those identified in Volition's most recent Annual Report on Form 10-K and Quarterly Reports on Form 10-Q, as well as other documents that Volition files with the Securities and Exchange Commission. These statements are based on current expectations, estimates and projections about Volition's business based, in part, on assumptions made by management. These statements are not guarantees of future performance and involve risks, uncertainties and assumptions that are difficult to predict. Forward-looking statements are made as of the date of this release, and, except as required by law, Volition does not undertake an obligation to update its forward-looking statements to reflect future events or circumstances.

Nu.Q®, rNuQ™, Nucleosomics™, Capture-PCR™, and Capture-Seq™ 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 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.

Cision View original content:https://www.prnewswire.com/news-releases/volitionrx-announces-data-showing-the-prognostic-value-of-its-nuq-cancer-test-302819291.html

SOURCE VolitionRx Limited

FAQ

What did Volition (VNRX) announce on July 7, 2026 about its Nu.Q® Cancer test?

Volition announced new clinical data showing prognostic value of its Nu.Q® Cancer Assay in newly diagnosed lung cancer. According to Volition, the test may help predict survival, progression-free survival, and identify patients more likely to benefit from curative treatment options.

How could Volition’s Nu.Q® Cancer test benefit lung cancer patients and clinicians?

Nu.Q® Cancer could offer clinicians an additional tool to inform treatment selection and monitoring in non-small cell lung cancer. According to Volition, measuring methylated nucleosome levels may aid survival assessment, progression-free survival estimation, and selection of patients for potentially curative care pathways.

What regulatory and reimbursement steps has Volition (VNRX) completed for Nu.Q® Cancer in France?

Volition reports that clinical certification of Nu.Q® Cancer at Hospices Civils de Lyon is completed. According to Volition, the company is preparing a reimbursement dossier under France’s RIHN framework, with an eligibility decision expected within five months once the dossier is deemed admissible.

What revenue per test does Volition (VNRX) anticipate for Nu.Q® Cancer?

Volition anticipates approximately €50 in revenue per Nu.Q® Cancer test in a direct sales model. According to Volition, this expectation relates to potential commercialization with hospital networks, alongside possible licensing agreements with third-party collaborators in the human cancer diagnostics field.

When might Volition’s Nu.Q® Cancer test enter routine clinical use in France?

Routine clinical use in France is linked to securing reimbursement under the RIHN framework. According to Volition, reimbursement would be a major milestone, and once achieved, the company anticipates introduction of Nu.Q® Cancer into routine clinical practice at French healthcare institutions.