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VolitionRx Secures EUR 2.0 Million of Non-Dilutive Funding from Regional Government Agencies in Belgium
Prnewswire· 2026-03-31 12:16
Core Insights - VolitionRx Limited has secured €2.0 million (approximately $2.3 million) in non-dilutive funding from regional government agencies in Belgium to support its ongoing development efforts [1][2]. Funding Details - The financing will be utilized for the development of the Nu.Q® product portfolio, including the regulatory transition program for Nu.Q® NETs and the research and development of a Lateral Flow product aimed at improving access in Low Income Countries [2]. - The total non-dilutive funding received by Volition to date exceeds $25 million, with this latest funding being part of a strategy to seek favorable terms for cash support [3][4]. Strategic Goals - The funding aims to enhance Volition's manufacturing capabilities and strengthen its research and development activities in Wallonia, Belgium [3]. - Key value inflection points targeted by this financing include clinical validation and the expansion of commercialization efforts for Volition's technologies [3]. Company Overview - VolitionRx is focused on advancing epigenetics to improve early detection and monitoring of diseases, including cancers and conditions associated with NETosis [4]. - The company is developing cost-effective blood tests that have the potential to enhance patient outcomes and quality of life through earlier detection [4].
Volition Announces Detection of Over 95% of Early-Stage Cancers
Prnewswire· 2026-03-25 12:17
Core Insights - VolitionRx Limited has announced significant proof of concept data demonstrating the ability to detect over 95% of early-stage cancers using its Capture-Seq™ technology [1][2][4] Company Overview - Volition is a multi-national epigenetics company focused on advancing the science of epigenetics and aims to improve outcomes for people and animals through earlier disease detection and monitoring [9][10] Technology and Methodology - The Capture-Seq™ technology enriches and purifies plasma samples to yield virtually pure circulating tumor DNA (ctDNA) for analysis, overcoming the challenge of high levels of non-cancerous DNA in blood samples [7][8] - A new two-step method has been developed to prepare pure ctDNA data sets, achieving over 99% purity in cancer-derived plasma DNA sequences [8][11] Clinical Validation - In a blinded validation cohort of 81 subjects, the detection rates for early-stage cancers were reported as follows: Stage I at 94%, Stage II at 96%, Stage III at 100%, and Stage IV at 91% [2][15] - Overall sensitivity for all stages was 93% and specificity for healthy controls was 95% [2][15] Market Potential - The Total Addressable Market (TAM) for early cancer detection is estimated at approximately $36 billion, with a significant commercial opportunity for Multi-Cancer Early Detection (MCED) and Minimal Residual Disease (MRD) detection [3][6][16] - The annualized TAM for human MCED use is projected to be around $23 billion, while MRD detection could represent over $13 billion [6][16] Strategic Partnerships - The company is in active discussions with several large liquid biopsy and diagnostic companies to expedite the development and launch of the Capture-Seq™ technology [6][16]
Volition Reports Breakthrough in Liquid Biopsy: Achievement of over 99% Purity in Isolating Cancer DNA
Prnewswire· 2026-03-18 12:17
Core Insights - VolitionRx Limited has achieved a breakthrough in liquid biopsy technology by isolating over 99% pure circulating tumor-derived DNA (ctDNA) from blood plasma samples, addressing a significant challenge in distinguishing cancer DNA from healthy DNA [1][2][4]. Technology and Methodology - The new technology, named "Capture-Seq™," utilizes a two-step method involving physical enrichment of samples and bioinformatic removal of non-tumor cfDNA sequences, resulting in virtually pure cancer DNA [4][5]. - This method is expected to facilitate the development of a novel class of liquid biopsy sequence biomarkers, potentially leading to multi-cancer early detection and monitoring of Minimal Residual Disease (MRD) [6][9]. Clinical Validation - Initial validation results are promising, with the technology detecting 49 out of 49 cancers in one cohort, including early-stage cancers, and 13 out of 14 later-stage cancers in a second cohort, with no false positives reported [7][8]. Market Potential - The total addressable market (TAM) for early cancer detection is estimated at $36 billion, while the market for MRD detection is projected to be over $13 billion annually [6][9]. - The company is actively engaging with global diagnostic leaders to accelerate the commercialization of this technology [6][10]. Company Overview - VolitionRx is focused on advancing epigenetics science and aims to improve disease detection and monitoring through innovative blood tests [11][12].
VolitionRx Secures $2.0 Million in Funding
Prnewswire· 2026-01-08 14:15
Core Viewpoint - VolitionRx Limited has entered into an amended agreement with Lind Global Asset Management to secure $2,000,000 in funding through the issuance of a senior secured convertible promissory note and a common stock purchase warrant, enhancing its financial position for future growth [1][2]. Group 1: Financial Details - The company will issue a senior secured convertible promissory note with a principal amount of $2,400,000 and a common stock purchase warrant to purchase up to 7,000,350 shares at an exercise price of $0.5714 per share [1]. - The 2026 Note will be repaid in eighteen monthly installments of $133,333 starting six months after issuance, with the option for the investor to increase payments up to $1,000,000 for two months [3]. - A commitment fee of $70,000 will be paid to the investor, deducted from the funding received [1]. Group 2: Previous Agreements - The amended agreement updates a previous securities purchase agreement from May 15, 2025, where the company issued a senior secured convertible promissory note of $7,500,000 and a warrant for 13,020,834 shares [2]. - Both the 2025 and 2026 Notes are secured by the assets of the company and its subsidiaries [2]. Group 3: Regulatory Compliance - The company is required to file a registration statement within 30 days of closing to cover the resale of shares issued upon conversion of the 2026 Note or exercise of the 2026 Warrant [4]. Group 4: Company Overview - Volition is a multi-national company focused on advancing epigenetics to improve early detection and monitoring of diseases, including cancers and conditions associated with NETosis [6][7]. - The company's research and development activities are primarily based in Belgium, with additional offices in the U.S. and London [8].
VolitionRX (NYSEAM:VNRX) Earnings Call Presentation
2026-01-08 12:00
Company Overview - VolitionRx is focused on saving lives and improving outcomes through low-cost testing in cancer, sepsis, and veterinary applications[4, 5] - The company operates with a low capex, low opex business model, emphasizing commercial partnerships and out-licensing[21] - VolitionRx leverages its IP Powerhouse with 56 patent families and a team with hundreds of years of experience[5] Commercialization and Licensing - The company received $10 million upfront and $13 million in milestone payments from an exclusive Element i+ in-house analyzer licensing partnership[29] - In 2024, Volition sold over 120,000 Nu.Q® Vet Cancer Tests & Components[40] - The company is targeting multiple licensing deals in the human space in 2026, focusing on upfront, milestone, and recurring revenue[25] Products and Market - Nu.Q® Vet is available in the United States, Europe, and Asia, detecting 76% of systemic cancers at 97% specificity[38, 40] - The company estimates a $170 million non-regulated animal testing licensing market, a $4 billion lab-developed screening/management market, and a >$3 billion ICU/ED CE Mark/FDA NETosis sales & licensing market[36] - Lung cancer screening and disease management with Nu.Q® is forecasted to reach over 3 million tests by 2035[63]
Volition Solves Liquid Biopsy's "Needle in a Haystack" Problem; Achieves 180-fold (18,000%) Enrichment
Prnewswire· 2025-12-11 14:00
Core Insights - VolitionRx Limited has announced a new manuscript detailing a novel method, Capture-Seq™, for detecting cancer biomarkers through the analysis of transcription factor protected cfDNA in plasma, which promises accurate and low-cost cancer tests [1][3][4] Technology and Methodology - The new method allows for the physical enrichment of ultrashort DNA fragments bound to transcription factors, achieving a 180-fold enrichment (18,000%) compared to traditional methods that lose the DNA's chromosomal context [2][4] - By isolating ultrashort transcription factor-bound DNA, Volition's technology effectively removes 99% of background DNA, addressing the challenge of interference in liquid biopsy tests for early-stage cancer [4][5] Clinical Results - In a small training cohort of 70 individuals, including 49 cancer patients, the analysis demonstrated 100% sensitivity and specificity in detecting cancer, including early-stage cases [7] Commercial Potential - The company sees significant commercial opportunities with a Total Addressable Market estimated at approximately $23 billion annually, and is actively seeking partnerships to accelerate the technology's integration and launch [9][10] Company Overview - VolitionRx is focused on advancing epigenetics and developing cost-effective blood tests for early disease detection and monitoring, with research and development activities centered in Belgium and additional offices in the U.S. and London [10][11]
VolitionRx Limited Announces Second Quarter 2025 Financial Results and Business Update
Prnewswire· 2025-08-14 20:10
Core Insights - 2025 is a crucial year for Volition as it aims to commercialize its Nu.Q® platform in the human diagnostics market, currently in discussions with over ten companies [1][2] - The company is progressing through various stages of partnership development, including due diligence and contract finalization, with expectations to sign its first agreement in the human diagnostics space this quarter [2][4] - Volition's Nu.Q® technology shows strong clinical evidence for applications in cancer and sepsis, which are areas of increasing interest for pharmaceutical companies [3][4] Business Strategy - The goal for 2025 includes securing multiple licensing agreements in the human diagnostics sector, similar to its successful strategy in the veterinary market, with diverse deal structures anticipated [4] - The company expects potential for upfront and milestone payments, as well as future recurring revenue from these agreements [4] Financial Performance - Volition recorded over $0.4 million in revenue for Q2 2025, marking a 15% growth compared to the same period last year [8] - The net loss decreased by 11% for the quarter and 24% for the first half of 2025 compared to the previous year [8] - Cash used in operating activities for the first half of 2025 was $10.6 million, down 30% year-over-year, with cash and cash equivalents totaling approximately $2.3 million as of June 30, 2025 [8]