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June 16, 2026 | Unsubscribe |
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Hello! |
New Alert: VolitionRx Limited (NYSE American: VNRX) |
VNRX is our new NYSE American biotech alert. |
This is a hidden gem opportunity that not many have seen – and we were amongst the first to bring it to your attention. |
Following our previous alert, the company rallied +53% in just over a week. |
Now, we believe it could be positioned for another big opportunity. |
VNRX trades for under 2.00 which means momentum can build very quickly. |
In addition, the company has announced multiple developments since our previous alert. |
VNRX is a NYSE American listed “multi-national epigenetics company” that 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”. |
Epigenetic changes can be detected before the diseased cells themselves become abnormal enough to show up in traditional biopsies, and oftentimes before the first symptoms are felt. |
VNRX is “dedicated to saving lives and improving outcomes for people and animals with life-altering diseases through earlier detection, disease and treatment monitoring”. |
The company’s “patented Nucleosomics™ technology” “detects characteristic epigenetic changes in nucleosomes that occur from the earliest stages of disease enabling early detection and potentially a better way to monitor disease progression and a patient’s response to treatment”. |
Based on this core, “cutting-edge technology” VNRX has “developed a portfolio of Nu.Q® assays which are simple, low-cost, accessible, routine blood tests”. |
Early detection and monitoring have the potential to not only prolong the life of patients, but also to improve their quality of life. |
Here is a number that puts everything else in context: |
Sadly, cancer is "a leading cause of death worldwide, accounting for nearly 10 million deaths in 2022." |
The single most powerful determinant of whether a patient survives is how early it is caught. |
Stage I survival rates for most cancers exceed 90%. |
By Stage IV, many of those same cancers drop below 20%. |
The problem has always been detection. |
Tumors are often invisible to standard diagnostics until they have already spread. |
VNRX is working to change that with a simple blood test. |
And on March 18, 2026 they released data that stopped us in our tracks: |
“Volition Reports Breakthrough in Liquid Biopsy: Achievement of over 99% Purity in Isolating Cancer DNA” |
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But that’s not all, on March 25, 2026 the company followed-up with another announcement: |
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This could be a ground floor opportunity that wall street has not yet discovered. |
As the company further explains: |
“The biggest problem facing liquid biopsy worldwide is that the vast majority of circulating DNA in blood plasma samples comes from healthy cells, not cancer cells.” |
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“In a world first new technology, Volition has overcome this hurdle and produced >99% pure cancer derived plasma DNA sequence sets for liquid biopsy.” |
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Dr Jake Micallef, Chief Scientific Officer, Volition commented: |
"Removal of background normal cell free DNA from the blood to reveal this level of tumor derived DNA has been a long term goal of liquid biopsy. I believe this is a world-first and could, in my opinion, represent the biggest scientific breakthrough in cancer testing and monitoring in recent years. |
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Furthermore: |
"These methodological and technological breakthroughs represent a novel liquid biopsy method for a novel class of potentially thousands of liquid biopsy sequence biomarkers”. |
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VNRX calls this “technology "Capture-Seq™" and it shows potential for both a multi-cancer early detection (MCED) approach, either alone or in combination with other tests, and the detection of Minimal Residual Disease”. |
Mr. Gael Forterre, Chief Commercial Officer, Volition added: |
"This scientific breakthrough has generated a lot of interest with potential licensing partners.” |
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In the subsequent March 25, 2026 press release VNRX released “the data from a blinded validation cohort of 81 subjects (colorectal and lung cancer patients = 59, healthy controls = 22) and are extremely encouraged by the results, particularly in early-stage cancer detection”. |
“Details are summarized in the table below: |
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The company believes “this technology could, with further development, become very widely used, in both the human and veterinary markets, and fits very well with our Nu.Q® product portfolio”. |
Capture-Seq is the emerging breakthrough - but it sits on top of a platform that is already generating real revenue and real clinical traction across multiple product lines: |
Nu.Q Vet Cancer Test is an “accessible and affordable screening test to aid in the early detection of cancer in dogs”. Nu.Q NETs assay is a “groundbreaking CE-marked diagnostic solution that clinicians can use to detect NETosis”. Nu.Q® Discover is an “invaluable research tool for R&D professionals working within the field of Pharmacoepigenetics, studying the epigenetic basis for variation in response to drugs”. Nu.Q® Cancer “encapsulates a range of simple, cost effective blood-based assays”
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The company has announced multiple accomplishments recently. |
Key highlights from May 27, 2026 press release: |
“First Quarter Revenue Growth: Reported $1M of revenue in the first quarter of 2026, representing a 300% increase year-over-year.” “Feline Lymphoma Manuscript Submission: Formally submitted the clinical manuscript for the Nu.Q® Vet cancer test in cats; $5 million milestone payment anticipated subsequent to publication.” “Global Licensing Momentum: Company confirms active discussions with more than a dozen of the world's leading diagnostic and liquid biopsy companies, including for technical evaluations.” “Capture-Seq™ Platform: Paper submitted for peer review; validation cohort detected over 95% of Stage I and II cancers2; underscores a $23 billion1 annualized opportunity in cancer detection.” “Sepsis & NETosis Validation: Inclusion of the Nu.Q® NETs assay in the $7.3 million government-backed DETECSEPS program in France.” “Breakthrough Finger-Prick Detection of Nucleosomes: Expanding global market potential for sepsis testing using lateral flow.” “European Lung Cancer Reimbursement: Formal reimbursement submission in France remains on schedule, with routine clinical use expected by end of 2026.”
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Unfortunately, “1 in 5 deaths worldwide are associated with sepsis”, the “body’s overactive and toxic response to an infection”. |
It is the “number 1 cause of death in hospitals” and contributes to a healthcare cost of “$62bn pa in USA alone”. |
Mr. Cameron Reynolds, Chief Executive Officer, Volition said: |
"The ability to rapidly identify high-risk patients at the Point-of-Care by quantifying their nucleosome levels using a finger-prick sample and simple lateral flow device could enable quicker clinical decision making and consequently better patient outcomes. |
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"This is a potential gamechanger, not only in diseases where time is critical such as sepsis, but also in significantly expanding potential use cases beyond traditional hospital infrastructure. It also creates a compelling pathway into underserved low-income countries, where laboratory infrastructure may be weak or non-existent." |
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On May 14, 2026, the company announced: |
“VolitionRx Limited Announces First Quarter 2026 Financial Results and Business Update” |
Cameron Reynolds, President and Group Chief Executive Officer, said: |
"We have made strong progress across all of our product pillars during the first quarter and indeed subsequent to quarter end. |
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"We announced the submission for peer review of a clinical manuscript reporting the high accuracy of our Nu.Q® Vet feline prototype assay in detecting lymphoma in cats, our third species. The publication of this study in a peer reviewed journal is expected subsequently to unlock a $5 million contractual milestone payment. The feline test could greatly expand the market of our Nu.Q® Vet platform. |
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"We are working with our long-term collaborators at the Hospices Civils de Lyon, one of Europe's leading cancer centers, on the reimbursement submission for Nu.Q® Lung Cancer. Reimbursement is the last step on the path to the first use of Nu.Q® in routine clinical practice, an exciting prospect which is core to Volition's mission, using our tests to help save lives. |
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"We reported two new, potentially large, clinical use cases for our Nu.Q® NETs assay beyond sepsis. In conjunction with the Mayo Clinic[1], we demonstrated Nu.Q® NETs' potential clinical utility in aiding early risk identification which could inform targeted preventive strategies in acute trauma care. We also demonstrated potential use for patient management of a chronic disease, Hidradenitis Suppurativa,[2] which affects about 1% of the world's population. Both use cases have the potential to be large markets. |
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"We are currently in discussions with more than a dozen of the world's leading diagnostic and liquid biopsy companies where our goal is to enter into licensing agreements and other arrangements that will bring revenue in the form of up front milestone payments, royalties and/or other recurring revenue. |
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"We are delighted to have grown the commercial interest in the first quarter, particularly with regards to our Capture-Seq™ technology, with an increase in discussions, including for technical evaluations. |
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"Discussions are at various stages of the negotiation process across all our different pillars; our laser focus is on executing licensing agreements and we will update you as they progress." |
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On May 27, the company announced: |
“VolitionRx Highlights Commercial Momentum and Multi-Pillar Execution Across $27+ Billion Total Addressable Markets” |
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Here are some of the company’s comments from this press release: |
“We have developed a truly remarkable, versatile platform and have further strengthened our Intellectual Property portfolio as we continue our licensing discussions with more than a dozen of the world's leading diagnostic and liquid biopsy companies. Our goal is to enter into licensing agreements and other arrangements that will bring revenue in the form of up front milestone payments, royalties and/or other recurring revenue.” |
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“We are delighted to have grown the commercial interest in the first quarter, particularly with regards to our Capture-Seq™ technology, with an increase in discussions, including for technical evaluations. Discussions are at various stages of the negotiation process across all our different pillars; our laser focus is on executing licensing agreements and we will update you as they progress.” |
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“Our vision is for our technologies to be incorporated into tests that will be used first by millions, and ultimately, hundreds of millions of people and animals a year, with our platform licensed to a range of large diagnostic and liquid biopsy companies (and governments) worldwide. Combining our groundbreaking technology with their installed base of laboratories, analyzer machines and sales forces around the world will achieve the optimal outcome for us – large companies have the resources to realize the opportunities better than Volition.” |
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In addition, two weeks ago, the company announced: |
“VolitionRx Files New Patent Protecting its Nu.Q® NETs Test for Ebola Triage and Treatment Monitoring” |
Dr. Jake Micallef, Chief Scientific Officer, Volition commented: |
"This filing yet again shows the breadth of utility of our technology: it claims the potential use of Volition's existing Nu.Q® NETs test for Ebola. The Nu.Q® NETs test quantifies circulating nucleosomes and Neutrophil Extracellular Traps (NETs) as early indicators of hyper-inflammation leading to septic shock and early mortality. |
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"Our existing patented product portfolio includes the CE-Marked automated Nu.Q® NETs assay for use in centralized laboratories, in addition to the recently announced capillary blood finger-prick lateral flow detection (LFT). The LFT could offer an unprecedented bedside triage solution for severe filovirus outbreaks, creating a compelling pathway into underserved, resource constrained countries, where laboratory infrastructure may be weak or non-existent. |
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"While existing Ebola diagnostics focus entirely on identifying the presence of the virus, Volition's technology focuses on the host's dysregulated immune response. The Nu.Q® NETs test measures H3.1 nucleosomes, which serve as an independent predictor of organ failure and mortality in patients with sepsis and COVID-19. Similarly, identification of elevated NETs levels prior to clinical deterioration may help field medics prevent disease spread and provide earlier, more effective treatment for Ebola-infected patients." |
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Last week, the company announced: |
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We believe VNRX could be positioned for big upside potential. |
Make sure to do your own due diligence. |
Sources: S, WHO, Cancer, Presentation, PR1, PR2, PR3, PR4, PR5, PR6, PR7, PR8, PR9, PR10, PR11, PR12, PR13, PR14, PR15, PR16, PR17, Website, Chart |
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Happy Trading! |
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UltimateStockAlerts Team |
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Note: We encourage all traders and investors to develop personal trading rules that you can follow and that work for you. Always protect your downside and note that we alert extremely volatile short-term opportunities. Before investing in securities, you should always consult with your financial, tax and legal advisor and never invest money you cannot afford to lose. |
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