Virax Biolabs Group Ltd (VRAX)

Virax Biolabs Reports Positive Early Clinical Data for ViraxImmune™ in Long COVID and Related Post-Acute Infection SyndromesMay 26, 2026 7:30 AM
PR Newswire (US) LONDON, May 26, 2026 /PRNewswire/ -- Virax Biolabs Group Limited (NASDAQ: VRAX) ("Virax" or the "Company") today reported positive early pilot performance data for ViraxImmune™, its blood-based test in development for Long COVID, myalgic encephalomyelitis/chronic fatigue syndrome ("ME/CFS") and related post-acute infection syndromes ("PAIS"). In the pilot dataset, ViraxImmune™ demonstrated measurable separation between PAIS patients and healthy controls, achieving 88% specificity and 92% positive predictive value ("PPV") — early performance metrics that Virax believes support continued development and advancement into larger clinical validation. Based on estimates derived from CDC, the RECOVER Initiative and other peer-reviewed and public-health sources, Virax estimates that up to 21 million adults in the United States may currently be living with Long COVID and related PAIS conditions, with approximately 2.5 million new cases estimated each year. Virax believes this represents a significant potential U.S. testing opportunity in an area where many patients are often assessed through symptoms and exclusion, rather than objective immune biomarkers of the type ViraxImmune™ is being developed to assess.Highlights:In the pilot dataset, ViraxImmune™ demonstrated measurable separation between PAIS patients and healthy controls and achieved 88% specificity and 92% positive predictive value ("PPV").ViraxImmune™ has now been evaluated in more than 120 subjects in the Company's ongoing UK clinical study in Long COVID, ME/CFS and related post-acute infection syndromes.Virax is preparing for its next major development milestone: a larger clinical validation analysis involving previously collected samples from 300 additional participants, with analysis expected to begin in Q4 2026 and results expected in Q1 2027.Findings support continued advancement toward Virax's intended U.S. market-entry strategy: an initial PAIS-focused U.S. Laboratory Developed Test ("LDT") route, with broader in vitro diagnostic ("IVD") development planned over time.If validated in larger studies, ViraxImmune™ could become one of the first objective immune-profiling approaches developed specifically for Long COVID, ME/CFS and related post-acute infection syndromes. Virax believes this approach could support a differentiated diagnostic strategy in an area of significant unmet need, with potential applications in patient stratification, clinical decision-making, longitudinal monitoring and therapeutic development."These early pilot data mark an important step in the development of ViraxImmune™ as a potential objective immune-profiling test for Long COVID, ME/CFS and related post-acute infection syndromes," said James Foster, Chairman and Chief Executive Officer of Virax Biolabs. "The observed separation between patients and healthy controls, together with encouraging early performance metrics, supports our confidence that ViraxImmune™ has the potential to address a major unmet diagnostic need as we advance toward our planned U.S. LDT-first route to market.""Patients with Long COVID, ME/CFS and related post-acute infection syndromes often face lengthy diagnostic journeys and limited objective testing options," said Dr. Sean Knight, MD, PhD, Principal Investigator at the Lydia Becker Institute of Immunology and Inflammation, University of Manchester, and Consultant Respiratory Physician at Northern Care Alliance NHS Foundation Trust. "Objective immune profiling may help improve how these patients are assessed, stratified and monitored over time. These early pilot findings are encouraging and support further clinical validation of ViraxImmune™."Virax will host an investor webcast on May 26, 2026, at 4:15 p.m. ET to review the early ViraxImmune™ dataset, discuss the clinical and commercial implications of the findings, and outline the Company's planned path toward larger clinical validation, assay finalization and U.S. market entry. Interested parties may register for the webcast at this link. A replay will be made available following the event.ViraxImmune™ is in development and is not approved for diagnostic use in any jurisdiction. The VRX003 observations are preliminary and are intended to inform ongoing assay development and future clinical validation planning.About Virax Biolabs Group LimitedVirax Biolabs Group Limited is a biotechnology company focused on the detection of immune responses to and diagnosis of viral diseases. The Company is developing T cell-based test technologies intended to support an immunology profiling platform. T cell testing may have applications in post-acute infection syndromes, including Long COVID, and other chronic conditions linked to immune dysregulation.For more information, please visit www.viraxbiolabs.comCaution Concerning Forward-Looking StatementsThis press release contains forward-looking statements. In addition, from time to time, we or our representatives may make forward-looking statements orally or in writing. We base these forward-looking statements on our expectations and projections about future events, which we derive from the information currently available to us. Such forward-looking statements relate to future events or our future performance, including: our financial performance and projections; our growth in revenue and earnings; and our business prospects and opportunities. You can identify forward-looking statements by those that are not historical in nature, particularly those that use terminology such as "may," "should," "expects," "anticipates," "contemplates," "estimates," "believes," "plans," "projected," "predicts," "potential," or "hopes" or the negative of these or similar terms.In evaluating these forward-looking statements, you should consider various factors, including: our ability to keep pace with new technology and changing market needs; potential for clinical trials to deliver statistically and/or clinically significant evidence of efficacy and/or safety, failure of preliminary, interim or top-line data to accurately reflect the complete results of a trial, failure of planned or ongoing preclinical and clinical studies to demonstrate expected results, potential failure to continue to secure FDA and other regulators' agreement on the regulatory path for ViraxImmune™ or other potential products; and the competitive environment of our business. These and other factors may cause our actual results to differ materially from any forward-looking statement. Forward-looking statements are only predictions. The forward-looking events discussed in this press release and other statements made from time to time by us or our representatives may not occur, and actual events and results may differ materially and are subject to risks, uncertainties, and assumptions about us.These forward-looking statements are based on information currently available to Virax and its current plans or expectations and are subject to a number of known and unknown uncertainties, risks and other important factors that may cause our actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements. These and other important factors are described in detail in the "Risk Factors" section of Virax's Annual Report on Form 20-F for the year ended March 31, 2025. Although we believe the expectations reflected in such forward-looking statements are reasonable, we can give no assurance that such expectations will prove to be correct. We are not obligated to publicly update or revise any forward-looking statement, whether as a result of uncertainties and assumptions. View original content to download multimedia:https://www.prnewswire.com/news-releases/virax-biolabs-reports-positive-early-clinical-data-for-viraximmune-in-long-covid-and-related-post-acute-infection-syndromes-302778628.htmlSOURCE Virax BioLabs Group Limited Original: Virax Biolabs Reports Positive Early Clinical Data for ViraxImmune™ in Long COVID and Related Post-Acute Infection Syndromes

I use own .14 month ago man...dammm

Typical Pump and dump: https://research.viraxbiolabs.com/

vrax................................p/m

$VRAX 💹

Virax Biolabs' CEO James Foster Outlines Strategic Priorities and Near-Term Milestones in Letter to ShareholdersApril 14, 2026 7:34 AM
PR Newswire (US)

Virax Biolabs is advancing a focused strategy centered on ViraxImmune™ and a U.S. market-entry pathway, which management believes is not reflected in the Company's current public valuation despite its balance sheet strength, debt-free position, recent financing and operational progress.LONDON, April 14, 2026 /PRNewswire/ -- Virax Biolabs Group Limited (NASDAQ: VRAX) ("Virax" or the "Company"), an innovative biotechnology company focused on immunology research and diagnostics, today published a shareholder letter from Chief Executive Officer James Foster and released an updated investor presentation. Together, these materials outline Virax's current strategic and commercial framework and the milestones management believes matter most over the next 90 to 180 days.







The Company's updated Q2 2026 investor presentation is available at: https://diagnostics.viraxbiolabs.com/virax-biolabs-q2-2026-investor-presentation/Highlights:Large under-served category: Virax believes post-acute infection syndromes ("PAIS"), including Long COVID, post-treatment Lyme disease ("PTLD") and myalgic encephalomyelitis / chronic fatigue syndrome ("ME/CFS"), represent a large, under-served diagnostic category with no widely adopted objective test in major markets and an estimated U.S. economic burden in excess of $25 billion.Our current focus: ViraxImmune™ is being developed to help identify immune dysfunction in PAIS using a novel, proprietary assay. Virax's current U.S. market-entry focus is a Laboratory Developed Test ("LDT") pathway, with broader in vitro diagnostic ("IVD") development intended to follow over time.Next catalyst: Management views the planned PAIS data readout on assay performance as the next key milestone in validating ViraxImmune™ and informing the Company's next steps toward U.S. market entry. The investor presentation sets out a validation-led timeline with 2026 focused on readout and partner study preparation.Operational progress: UK PAIS studies are fully recruited, the Company has completed its initial FDA pre-submission Q-Sub meeting and received feedback to inform strategy, U.S. clinical validation planning with Emory University is under way, and the Company has achieved ISO 13485 and ISO 9001 certification.Balance sheet support: Virax remains debt-free and management believes the Company has resources to execute through key near-term milestones.Valuation backdrop: Management expects Virax's unaudited cash position at March 31, 2026 to be approximately $6.4 million. As of April 10, 2026, Virax's market capitalisation was approximately $2.6 million, based on 19,923,432 outstanding shares. Management does not believe this valuation reflects the Company's debt-free balance sheet or progress toward key clinical and commercial milestones."Our task is to execute: advance the next phase of validation, continue building the U.S. market-entry pathway and let those milestones establish the Company's direction," said James Foster, Chairman and Chief Executive Officer of Virax Biolabs.The full text of Mr Foster's April 2026 shareholder letter is reproduced below.Dear Fellow Shareholders,Virax is entering a more execution-focused phase. In a difficult small-cap market, our priority is to clarify the opportunity, deliver the next key data milestone and continue building toward a practical U.S. market-entry path.Our near-term priorities are straightforward. We are concentrating the business on the areas we believe matter most to near-term value creation: a large under-served PAIS category with ViraxImmune™ as our lead product. An upcoming PAIS data readout will be an important milestone for ViraxImmune™ by helping assess whether the assay can distinguish immune dysfunction patterns in PAIS individuals relative to controls, and by informing the next phase of U.S. clinical validation planning.Execution and Strategic PositioningOver the past year, we have worked to move ViraxImmune™ from concept toward clinical, regulatory and operational readiness. That has included recruitment across our UK PAIS studies, FDA pre-submission engagement, U.S. clinical validation planning and, most recently, the strengthening of our quality infrastructure through ISO 13485 and ISO 9001 certification. Together, these steps are intended to support disciplined assay development and the validation work needed for future market entry.We continue to believe PAIS is a large, under-served diagnostic category with no widely adopted objective test in major markets. As our updated investor presentation sets out, millions of patients are affected, the estimated U.S. economic burden exceeds $25 billion, and the lack of objective testing continues to impair timely diagnosis, clinical management and therapeutic development. ViraxImmune™ is being developed to address that gap by helping identify immune dysfunction in PAIS through an objective test-based approach, which we believe could support clearer clinical assessment and treatment management over time. Against that backdrop, our objective is not to pursue every possible opportunity at once, but to focus on the indication, product and market-entry pathway we believe are most relevant to near-term value creation.In the United States, our current focus is on an LDT pathway as the initial market-entry route, with broader IVD development to follow over time. We believe this may offer the most practical way to establish an initial commercial foothold while continuing to build the clinical and regulatory package required for broader adoption. Our investor presentation also sets out the intended coding and reimbursement progression, beginning with an initial miscellaneous-code billing approach and, over time, potentially moving toward a PLA code and broader permanent coding framework if clinical utility and market penetration are established.Financial Position and ValuationOur balance sheet remains a core strength of the Company.Management expects Virax's unaudited cash position at March 31, 2026 to be approximately $6.4 million, with total assets of approximately $8.3 million and total liabilities of approximately $1.0 million, resulting in shareholders' equity of roughly $7.3 million and no long-term debt.As of April 10, 2026, Virax's market capitalisation was approximately $2.6 million, based on 19,923,432 outstanding shares. Based on these figures, the Company was trading below its cash balance and at a negative implied enterprise value (market capitalisation plus debt minus cash), which in our view suggests that the market was ascribing limited value to our clinical and commercial programmes, intellectual property, laboratory infrastructure and longer-term potential. While we cannot and do not make predictions about near-term share price movements, we do believe this disconnect does not reflect the underlying progress of the business, the balance sheet position of the Company, or the scale of the opportunity we are pursuing.With a healthy cash position, a modest liability profile and no term debt to service, we believe we are appropriately capitalised to deliver our near-term clinical and regulatory milestones and to continue executing the next phase of our strategy.Path ForwardOver the next 90 to 180 days, our priorities are clear: complete the rollout of our updated investor materials to improve communication of the Company's strategy and future potential to the market, deliver and contextualise the PAIS data readout, continue preparing the U.S. market-entry pathway, and use those milestones to support broader institutional and strategic engagement.The next phase is about validation and preparation. The current milestone sequence is centred on 2026 validation activities and, over time, potential U.S. LDT market entry followed by broader IVD development.Longer term, if the data and market engagement justify it, we believe this can support a broader value-creation path around ViraxImmune™ and the wider immune-profiling platform. For now, however, our focus is practical and near term: disciplined execution against defined milestones.Closing ThoughtsWe believe Virax should increasingly be judged on whether it can execute a credible sequence: operational readiness, data, market-entry pathway and disciplined capital strategy. That is the sequence we are now pursuing.Thank you for your continued support.Sincerely,James FosterChief Executive OfficerVirax Biolabs Group LimitedAbout Virax Biolabs Group LimitedVirax Biolabs Group Limited is an innovative biotechnology company focused on the detection of immune responses to and diagnosis of viral diseases. Virax Biolabs Group Limited is developing T cell-based test technologies with the intention of providing an immunology profiling platform. T cell testing can be particularly effective in the diagnosis and therapeutics of post-acute infection syndromes such as Long COVID and other chronic conditions linked to immune dysregulation.For more information, please visit www.viraxbiolabs.comCaution Concerning Forward-Looking StatementsThis press release contains forward-looking statements. In addition, from time to time, we or our representatives may make forward-looking statements orally or in writing. We base these forward-looking statements on our expectations and projections about future events, which we derive from the information currently available to us. Such forward-looking statements relate to future events or our future performance, including: our financial performance and projections; our growth in revenue and earnings; and our business prospects and opportunities. You can identify forward-looking statements by those that are not historical in nature, particularly those that use terminology such as "may," "should," "expects," "anticipates," "contemplates," "estimates," "believes," "plans," "projected," "predicts," "potential," or "hopes" or the negative of these or similar terms.In evaluating these forward-looking statements, you should consider various factors, including: our ability to keep pace with new technology and changing market needs; potential for clinical trials to deliver statistically and/or clinically significant evidence of efficacy and/or safety, failure of interim or top-line results to accurately reflect the complete results of a trial, failure of planned or ongoing preclinical and clinical studies to demonstrate expected results, potential failure to continue to secure FDA and other regulators' agreement on the regulatory path for ViraxImmune™ or other potential products; and the competitive environment of our business. These and other factors may cause our actual results to differ materially from any forward-looking statement. Forward-looking statements are only predictions. The forward-looking events discussed in this press release and other statements made from time to time by us or our representatives may not occur, and actual events and results may differ materially and are subject to risks, uncertainties, and assumptions about us.These forward-looking statements are based on information currently available to Virax and its current plans or expectations and are subject to a number of known and unknown uncertainties, risks and other important factors that may cause our actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements. These and other important factors are described in detail in the "Risk Factors" section of Virax's Annual Report on Form 20-F for the year ended March 31, 2025. Although we believe the expectations reflected in such forward-looking statements are reasonable, we can give no assurance that such expectations will prove to be correct. We are not obligated to publicly update or revise any forward-looking statement, whether as a result of uncertainties and assumptions.










View original content to download multimedia:https://www.prnewswire.com/news-releases/virax-biolabs-ceo-james-foster-outlines-strategic-priorities-and-near-term-milestones-in-letter-to-shareholders-302741286.htmlSOURCE Virax BioLabs Group Limited

Original: Virax Biolabs' CEO James Foster Outlines Strategic Priorities and Near-Term Milestones in Letter to Shareholders

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Virax Biolabs Achieves ISO Certifications, Laying Foundation for Regulated IVD Development and U.S. Clinical Validation

March 31, 2026

LONDON, March 31, 2026 /PRNewswire/ -- Virax Biolabs Group Limited (NASDAQ: VRAX) ("Virax" or the "Company") today announced that Virax Biolabs (UK) Limited, its wholly owned subsidiary, has achieved ISO 13485:2016 and ISO 9001:2015 certification for its quality management system. The certifications were issued by LRQA, with an issue date of 18 February 2026 and an expiry date of 17 February 2029.

Highlights:
• Virax believes the strengthened quality framework supports its post-acute infection syndromes ("PAIS") strategy by strengthening readiness for regulated in vitro diagnostic ("IVD") development and supporting U.S. clinical validation activities.
• Virax is also evaluating potential U.S. laboratory-based testing service offerings, which may include a laboratory-developed test ("LDT") pathway.

Within the scope of approval, ISO 13485:2016 covers the design and development of immunological assay components and kits, including antibody- and peptide-based reagents, for IVD applications. Within the scope of approval, ISO 9001:2015 covers the provision of manufacturing, design and development of Virax's research-use-only products and services.

ISO 13485 and ISO 9001 are internationally recognised quality management standards that establish a framework for design control, risk management, traceability, supplier qualification and manufacturing consistency. In simple terms, ISO 13485 is a widely used quality standard for medical devices and diagnostics, while ISO 9001 is a broader quality management standard used across many industries. Virax believes these certifications strengthen the controls and documentation needed to advance regulated diagnostics programmes and support clinical validation work.

Virax believes these certifications provide an important operational foundation for the Company's quality-managed development activities, including its in-development diagnostic technology for post-acute infection syndromes ("PAIS"), such as post-acute sequelae of SARS-CoV-2 ("PASC") (commonly referred to as "Long COVID"), and support the Company's broader strategy to build a T cell immune-profiling platform with a transatlantic clinical and regulatory footprint.

In parallel, Virax continues to advance its U.S. clinical validation work, which the Company believes is supported by a strengthened quality framework. As previously disclosed, Virax has entered into a Research Services Agreement ("RSA") with Emory University's ADJUST Center to conduct clinical studies of ViraxImmune™ focused on immune profiling in individuals with PASC (commonly referred to as "Long COVID"). Under the agreement, Emory will conduct laboratory testing and analysis to generate clinical data intended to inform Virax's regulatory planning and potential future commercial rollout.

Virax believes strengthening its quality systems is relevant to disciplined development and control of key assay components and supporting documentation processes, which can support validation activities and scale-up planning, subject to applicable regulatory requirements.

"Achieving ISO 13485 and ISO 9001 certification is a meaningful milestone for Virax," said James Foster, Chairman and Chief Executive Officer of Virax Biolabs. "It reflects the work our team has done to implement robust quality systems that support the regulated development of our immunological assays. This matters as we continue to execute our PAIS strategy, including strengthening the foundation for regulated IVD development and expanding our evidence base through UK and U.S. clinical programmes, while also evaluating potential U.S. laboratory-based testing pathways, which may include an LDT route."

About Virax Biolabs Group Limited
Virax Biolabs Group Limited is an innovative biotechnology company focused on the detection of immune responses to and diagnosis of viral diseases. Virax Biolabs Group Limited is developing T cell-based test technologies with the intention of providing an immunology profiling platform. T cell testing can be particularly effective in the diagnosis and therapeutics of post-acute infection syndromes, including Long COVID, and other chronic conditions linked to immune dysregulation.

For more information, please visit www.viraxbiolabs.com

Caution Concerning Forward-Looking Statements
This press release contains forward-looking statements. In addition, from time to time, we or our representatives may make forward-looking statements orally or in writing. We base these forward-looking statements on our expectations and projections about future events, which we derive from the information currently available to us. Such forward-looking statements relate to future events or our future performance, including: our financial performance and projections; our growth in revenue and earnings; and our business prospects and opportunities. You can identify forward-looking statements by those that are not historical in nature, particularly those that use terminology such as "may," "should," "expects," "anticipates," "contemplates," "estimates," "believes," "plans," "projected," "predicts," "potential," or "hopes" or the negative of these or similar terms.

In evaluating these forward-looking statements, you should consider various factors, including: our ability to change the direction of the Company; our ability to keep pace with new technology and changing market needs; and the competitive environment of our business. These and other factors may cause our actual results to differ materially from any forward-looking statement. Forward-looking statements are only predictions. The forward-looking events discussed in this press release and other statements made from time to time by us or our representatives may not occur, and actual events and results may differ materially and are subject to risks, uncertainties, and assumptions about us.

These forward-looking statements are based on information currently available to Virax and its current plans or expectations and are subject to a number of known and unknown uncertainties, risks and other important factors that may cause our actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements. These and other important factors are described in detail in the "Risk Factors" section of Virax's Annual Report on Form 20-F for the year ended March 31, 2025. Although we believe the expectations reflected in such forward-looking statements are reasonable, we can give no assurance that such expectations will prove to be correct. We are not obligated to publicly update or revise any forward-looking statement, whether as a result of uncertainties and assumptions, the forward-looking events discussed in this press release and other statements made from time to time by us or our representatives might not occur.

Cision View original content to download multimedia:https://www.prnewswire.com/news-releases/virax-biolabs-achieves-iso-certifications-laying-foundation-for-regulated-ivd-development-and-us-clinical-validation-302727405.html

SOURCE Virax BioLabs Group Limited

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Virax Biolabs Achieves ISO Certifications, Laying Foundation for Regulated IVD Development and U.S. Clinical ValidationMarch 31, 2026 7:34 AM
PR Newswire (US)

LONDON, March 31, 2026 /PRNewswire/ -- Virax Biolabs Group Limited (NASDAQ: VRAX) ("Virax" or the "Company") today announced that Virax Biolabs (UK) Limited, its wholly owned subsidiary, has achieved ISO 13485:2016 and ISO 9001:2015 certification for its quality management system. The certifications were issued by LRQA, with an issue date of 18 February 2026 and an expiry date of 17 February 2029.







Highlights:Virax believes the strengthened quality framework supports its post-acute infection syndromes ("PAIS") strategy by strengthening readiness for regulated in vitro diagnostic ("IVD") development and supporting U.S. clinical validation activities.Virax is also evaluating potential U.S. laboratory-based testing service offerings, which may include a laboratory-developed test ("LDT") pathway.Within the scope of approval, ISO 13485:2016 covers the design and development of immunological assay components and kits, including antibody- and peptide-based reagents, for IVD applications. Within the scope of approval, ISO 9001:2015 covers the provision of manufacturing, design and development of Virax's research-use-only products and services.ISO 13485 and ISO 9001 are internationally recognised quality management standards that establish a framework for design control, risk management, traceability, supplier qualification and manufacturing consistency. In simple terms, ISO 13485 is a widely used quality standard for medical devices and diagnostics, while ISO 9001 is a broader quality management standard used across many industries. Virax believes these certifications strengthen the controls and documentation needed to advance regulated diagnostics programmes and support clinical validation work.Virax believes these certifications provide an important operational foundation for the Company's quality-managed development activities, including its in-development diagnostic technology for post-acute infection syndromes ("PAIS"), such as post-acute sequelae of SARS-CoV-2 ("PASC") (commonly referred to as "Long COVID"), and support the Company's broader strategy to build a T cell immune-profiling platform with a transatlantic clinical and regulatory footprint.In parallel, Virax continues to advance its U.S. clinical validation work, which the Company believes is supported by a strengthened quality framework. As previously disclosed, Virax has entered into a Research Services Agreement ("RSA") with Emory University's ADJUST Center to conduct clinical studies of ViraxImmune™ focused on immune profiling in individuals with PASC (commonly referred to as "Long COVID"). Under the agreement, Emory will conduct laboratory testing and analysis to generate clinical data intended to inform Virax's regulatory planning and potential future commercial rollout.Virax believes strengthening its quality systems is relevant to disciplined development and control of key assay components and supporting documentation processes, which can support validation activities and scale-up planning, subject to applicable regulatory requirements."Achieving ISO 13485 and ISO 9001 certification is a meaningful milestone for Virax," said James Foster, Chairman and Chief Executive Officer of Virax Biolabs. "It reflects the work our team has done to implement robust quality systems that support the regulated development of our immunological assays. This matters as we continue to execute our PAIS strategy, including strengthening the foundation for regulated IVD development and expanding our evidence base through UK and U.S. clinical programmes, while also evaluating potential U.S. laboratory-based testing pathways, which may include an LDT route."About Virax Biolabs Group LimitedVirax Biolabs Group Limited is an innovative biotechnology company focused on the detection of immune responses to and diagnosis of viral diseases. Virax Biolabs Group Limited is developing T cell-based test technologies with the intention of providing an immunology profiling platform. T cell testing can be particularly effective in the diagnosis and therapeutics of post-acute infection syndromes, including Long COVID, and other chronic conditions linked to immune dysregulation.For more information, please visit www.viraxbiolabs.comCaution Concerning Forward-Looking StatementsThis press release contains forward-looking statements. In addition, from time to time, we or our representatives may make forward-looking statements orally or in writing. We base these forward-looking statements on our expectations and projections about future events, which we derive from the information currently available to us. Such forward-looking statements relate to future events or our future performance, including: our financial performance and projections; our growth in revenue and earnings; and our business prospects and opportunities. You can identify forward-looking statements by those that are not historical in nature, particularly those that use terminology such as "may," "should," "expects," "anticipates," "contemplates," "estimates," "believes," "plans," "projected," "predicts," "potential," or "hopes" or the negative of these or similar terms.In evaluating these forward-looking statements, you should consider various factors, including: our ability to change the direction of the Company; our ability to keep pace with new technology and changing market needs; and the competitive environment of our business. These and other factors may cause our actual results to differ materially from any forward-looking statement. Forward-looking statements are only predictions. The forward-looking events discussed in this press release and other statements made from time to time by us or our representatives may not occur, and actual events and results may differ materially and are subject to risks, uncertainties, and assumptions about us.These forward-looking statements are based on information currently available to Virax and its current plans or expectations and are subject to a number of known and unknown uncertainties, risks and other important factors that may cause our actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements. These and other important factors are described in detail in the "Risk Factors" section of Virax's Annual Report on Form 20-F for the year ended March 31, 2025. Although we believe the expectations reflected in such forward-looking statements are reasonable, we can give no assurance that such expectations will prove to be correct. We are not obligated to publicly update or revise any forward-looking statement, whether as a result of uncertainties and assumptions, the forward-looking events discussed in this press release and other statements made from time to time by us or our representatives might not occur.



View original content to download multimedia:https://www.prnewswire.com/news-releases/virax-biolabs-achieves-iso-certifications-laying-foundation-for-regulated-ivd-development-and-us-clinical-validation-302727405.htmlSOURCE Virax BioLabs Group Limited

Original: Virax Biolabs Achieves ISO Certifications, Laying Foundation for Regulated IVD Development and U.S. Clinical Validation

VRAX....................................https://stockcharts.com/sc3/ui/?s=VRAX&p=w&b=5&g=0&id=p86431144783

Out. Took a 3 1/2% hit.

VRAX.....Bought the dip. In @ .57

.65 one more round 

.68

.58 one more round to play here like yesterday 

Virax Biolabs' CEO James Foster Outlines Clinical Progress and 2026 Priorities in Latest Annual Letter to Shareholders
Virax Biolabs' proprietary in-development diagnostic technology for post-acute infection syndromes ("PAIS"), such as Long COVID, positions the Company for an important data year ahead, following a series of recent clinical and operational milestones over the past 12 months.

LONDON, Dec. 3, 2025 /PRNewswire/ -- Virax Biolabs Group Limited (NASDAQ: VRAX) ("Virax" or the "Company"), an innovative biotechnology company dedicated to the advancement of immunology research and diagnostics, today highlighted key milestones, achievements and clinical progress while outlining its strategic priorities for 2026 in a letter to shareholders and investors.


Post-acute infection syndromes ("PAIS") – including Long COVID, myalgic encephalomyelitis / chronic fatigue syndrome ("ME/CFS") and post-treatment Lyme disease ("PTLD") – present a major healthcare challenge globally. In his letter to stakeholders and investors, Virax CEO James Foster outlines the Company's significant clinical progress in PAIS diagnostic development, alongside its financial position. Management believes this reflects a strong platform and tangible product potential for the ViraxImmune™ programme.

The letter looks back on the past year and sets out goals for 2026. It describes Virax Biolabs' transition from planning to execution across its core strategic programmes, the deepening of its scientific data package, and the advancement of U.S. and UK regulatory pathways. Key clinical and operational milestones highlighted in the letter include:

UK Clinical Study Recruitment Completion: Full recruitment into its first UK clinical study (VRX-002) was completed ahead of schedule, with initial data expected in Q2 2026.
New UK Trial Initiation: Initiation of a second UK-based trial (VRX-003) in PAIS, which is now fully enrolled.
U.S. Research Collaboration: Establishment of a clinical collaboration with Emory University (ADJUST Center and ELIAD) to support U.S. regulatory and potential commercial plans in post-acute sequelae of COVID-19 (PASC, or Long COVID).
ImmuneSelect RUO expansion: Continued development of the ImmuneSelect research-use-only ("RUO") portfolio of immune-profiling reagents, which can be commercialised for research use without waiting for diagnostic approvals and has the potential to contribute to near-term revenue as adoption builds among research and biopharmaceutical customers.
Solid Balance Sheet: A debt-free balance sheet with sufficient cash on hand to execute near-term commercial and scientific priorities.
"The past year has been about execution – moving from plans on paper to recruited patients, generated data, regulatory engagement and strengthened institutional partnerships," said James Foster, Chairman and Chief Executive Officer of Virax Biolabs.

Virax Biolabs' progress and partnerships demonstrate the Company's commitment to advancing immunology research, developing what we believe to be a first-of-its-kind PAIS diagnostic, and building value for its stakeholders throughout 2026.

The full text of Mr Foster's 2025 Annual Letter to Shareholders is reproduced below.

Dear Fellow Shareholders,

As we close out 2025 and look ahead to the next phase of Virax Biolabs' journey, I am pleased to share an update on our progress and our priorities for the coming years. Over the past twelve months, we have moved from plans to execution across our core programmes – completing recruitment for our first UK clinical study, deepening our scientific data package, strengthening our U.S. and UK regulatory pathways, and reinforcing the balance sheet to support these activities.

Our strategic goal remains unchanged: to build a leading immune-profiling platform focused on T cell diagnostics and functional immune monitoring in post-acute infection syndromes, protective immunity and related areas of chronic immune dysfunction.

In 2026, our focus is on three core catalysts: delivering initial data from our UK PAIS study to support our planned UK regulatory submission; initiating the U.S. clinical study with Emory University in post-acute sequelae of COVID-19 ("PASC", also known as long COVID); and expanding commercial uptake of our ImmuneSelect research-use-only ("RUO") products as a potential nearer-term revenue driver and as a tool to improve understanding of immune system health globally.

Major Developments in 2025

Over the year, we announced the initiation of our first UK clinical validation study (VRX-002), the presentation of new T cell dysfunction data at WIRM in Davos, the launch of a long COVID collaboration with Emory University in the U.S., and continued strengthening of our scientific and clinical infrastructure. In addition, we initiated a second UK-based clinical study (VRX-003) in PAIS to support our planned regulatory submissions.

Advancing the ViraxImmune™ clinical programme and ImmuneSelect research portfolioIn March, we announced that we had enrolled the first patients into our UK multicentre clinical study ( https://clinicaltrials.gov/study/NCT06731179 ), involving 160 subjects and evaluating the ViraxImmune™ T cell assay in PAIS, including long COVID, post-treatment Lyme disease ("PTLD"), and ME/CFS. This multi-site study, involving five clinical centres and run in collaboration with the National Health Service ("NHS"), is designed to generate the clinical data required to support planned regulatory submissions and ultimately to help inform patient care over time. Additionally, in April we initiated our second UK-based clinical study in PAIS, involving 100 subjects and run by Eurofins, which is now fully enrolled.Shortly thereafter, we presented mechanistic data on T cell exhaustion and dysfunction in PAIS at the 19th World Immune Regulation Meeting ("WIRM") in Davos, Switzerland. These data showed progressive up-regulation of multiple exhaustion markers (PD-1, LAG-3, TIGIT, TIM-3, CD39) with repeated antigen stimulation, alongside changes in cytokine profiles in PAIS patients versus healthy controls. In simple terms, the findings suggest that many PAIS patients show clear signs of ongoing T cell dysfunction, which is consistent with the type of immune dysfunction that ViraxImmune™ is designed to characterise. We had previously announced our participation at WIRM as an important opportunity to showcase our immune-profiling portfolio to the scientific community.In November, we reported a key operational milestone: completion of patient recruitment for the UK clinical study ahead of schedule, reaching the full target of 160 participants across long COVID, PTLD and ME/CFS cohorts. The collected samples are now undergoing detailed immunological analysis. We expect initial read-outs from this longitudinal study in the second quarter of 2026. These results are intended to support our planned submissions to the UK Medicines and Healthcare products Regulatory Agency ("MHRA") and to inform subsequent regulatory pathways.Taken together, the progress in 2025 has significantly reduced the clinical execution risk for ViraxImmune™ and positioned us for an important data year ahead.Alongside ViraxImmune™, we have continued to develop our ImmuneSelect RUO portfolio of peptide pools, ELISpot plates and related reagents. While still at an early stage, this offering already supports revenue-generating opportunities with laboratories and researchers working on chronic infection, inflammation and immune dysfunction. Because these are RUO reagents rather than diagnostic tests, they are for research use only and can be commercialised without waiting for diagnostic approvals, offering the potential to contribute to revenue in the near term as we build adoption among research and biopharmaceutical customers. We see ImmuneSelect as both a standalone commercial opportunity in the research and biopharmaceutical markets and a complementary channel for expanding awareness and adoption of the ViraxImmune™ platform over time.
Building a transatlantic regulatory and clinical footprintIn parallel with our UK work, we have made meaningful advances in the United States. In August, we announced a Research Services Agreement with Emory University's ADJUST Center and the Emory Laboratory for Innovative Assay Development ("ELIAD"). Under this agreement, Emory will conduct clinical studies of ViraxImmune™ focusing initially on post-acute sequelae of COVID-19 ("PASC", or long COVID), generating data to help inform our U.S. regulatory strategy and potential future commercial plans.This collaboration is closely linked to our engagement with the U.S. Food and Drug Administration ("FDA"). We used 2025 to prepare for and then hold an in-person pre-submission meeting ("Q-sub") with the FDA to discuss the proposed intended use and regulatory pathway for ViraxImmune™ in PASC, also known as long COVID. The final minutes from this meeting, received in the autumn, provided constructive feedback on our clinical and analytical development plans. We are incorporating this guidance as we design our planned U.S. clinical study with Emory University, which we anticipate initiating in 2026.
Financial Position and Valuation

Our balance sheet remains a core strength of the Company.

As of 30 September 2025, we held approximately $3.3 million in cash and cash equivalents, with total assets of $5.7 million and total liabilities of $0.6 million, resulting in shareholders' equity of roughly $5.1 million and no long-term debt.

At the time of writing, Virax's market capitalisation is approximately $1.7 million. Based on these figures, the Company is trading below its cash balance and at a negative implied enterprise value (market capitalisation plus debt minus cash), which in our view implies that the market is currently ascribing limited value to our clinical programmes, intellectual property, laboratory infrastructure and longer-term commercial potential. While we cannot and do not make predictions about near-term share price movements, we believe this disconnect does not reflect what we see as the intrinsic value of our assets, the underlying progress of the business, or the scale of the opportunity we are pursuing. Our focus remains on disciplined capital allocation and execution of our strategy, confident that sustained delivery over time is the most effective way to create long-term shareholder value.

With a healthy cash position, a modest liability profile and no term debt to service, we believe we are appropriately capitalised to deliver our near-term clinical and regulatory milestones.

Strategic Priorities for 2026 and Beyond

Looking ahead, our first priority is to deliver high-quality clinical data from the UK PAIS study. With recruitment now complete, we are focused on finalising the immunological analyses and currently expect to share initial data in Q2 2026, including at scientific meetings and, where appropriate, in peer-reviewed publications. In parallel, we plan to initiate U.S. clinical work with Emory University by finalising a protocol that reflects recent FDA feedback and beginning enrolment into a long COVID–focused study in 2026. Together, these programmes are intended to help establish a robust transatlantic evidence base for ViraxImmune™. In addition, we are evaluating potential U.S. laboratory-based testing service offerings for ViraxImmune™, through appropriate laboratories and subject to applicable regulatory requirements, as a way to begin building early clinical experience and market familiarity with the assay, if pursued.

We will continue to progress our regulatory pathways in both the UK and the U.S., and emerging clinical and analytical data from these programmes will be used to prepare for interactions with the MHRA and subsequent submission steps. At the same time, we will maintain an active dialogue with the FDA as our data package matures, with the aim of helping to define a potential path for ViraxImmune™ in long COVID and related indications.

We also intend to expand our immune-profiling platform and partnerships. This includes growing the ImmuneSelect RUO portfolio and its distribution network, with the goal of building a recurring, diversified RUO revenue base over time, and exploring collaborations that apply ViraxImmune™ and ImmuneSelect to vaccine response, protective immunity and oncology. Across all of this, we remain disciplined in how we deploy capital—prioritising spending on activities that move us toward clear clinical, regulatory and commercial milestones, and seeking non-dilutive funding and strategic partnerships wherever possible to support the platform while protecting shareholder value.

Closing Thoughts

The past year has been about execution – moving from plans on paper to enrolled patients, generated data, regulatory engagement and strengthened institutional partnerships. We now enter 2026 with what we believe is a clearer clinical path, a stronger scientific story and the resources to pursue our next set of milestones.

On behalf of the Board and the entire Virax team, I would like to thank you for your continued support and patience during what we recognise has been a challenging market environment for small-cap biotech. We remain firmly committed to our mission of developing meaningful immune-profiling diagnostics for patients suffering from post-acute infection syndromes and related immune-mediated conditions, and to building long-term value for all our stakeholders.

Sincerely,

James Foster

Chairman and Chief Executive Officer

Virax Biolabs Group Limited

Virax Biolabs Group Limited is an innovative biotechnology company focused on the detection of immune responses to and diagnosis of viral diseases. Virax Biolabs Group Limited is developing T cell-based test technologies with the intention of providing an immunology profiling platform. T cell testing can be particularly effective in the diagnosis and therapeutics of post-acute infection syndromes such as long COVID and other chronic conditions linked to immune dysregulation.

For more information, please visit www.viraxbiolabs.com

Caution Concerning Forward-Looking Statements

This press release contains forward-looking statements. In addition, from time to time, we or our representatives may make forward-looking statements orally or in writing. We base these forward-looking statements on our expectations and projections about future events, which we derive from the information currently available to us. Such forward-looking statements relate to future events or our future performance, including: our financial performance and projections; our growth in revenue and earnings; and our business prospects and opportunities. You can identify forward-looking statements by those that are not historical in nature, particularly those that use terminology such as "may," "should," "expects," "anticipates," "contemplates," "estimates," "believes," "plans," "projected," "predicts," "potential," or "hopes" or the negative of these or similar terms.

In evaluating these forward-looking statements, you should consider various factors, including: our ability to change

Back in .60 back out .78 on next 5min candle

VRAX,,,,..........p/m

.60

Cash out for 6% gains at .52

Up 15%

.52 now going 

Let s pump in some quick flip

$VRAX penny bio with just 2.8m marketcap and 3m float & 0.89 cash per share with 9% short interest and only 50k borrows on IBKR

- Virax plans to hold a pre-submission meeting with the FDA in early September 2025.

Virax Biolabs is preparing for a pre-submission meeting with the FDA to discuss the regulatory pathway for ViraxImmune™.

- last offering was at 4.50 & the lowest warrants are at 2.93 with customary anti-dilution price protection so can't adjust exercise price lower

- has until January 12, 2026 for 1.00 compliance so plenty of time

Partnering with Emory University pump Emory University last long and long Covid...
http://www.facebook.com/sharer.php?s=100&p[url]=https%3A%2F%2Finvestorshub.advfn.com%2Fstock-market%2FNASDAQ%2Fvirax-biolabs-VRAX%2Fstock-news%2F96702238%2Fvirax-biolabs-partners-with-emory-university-on-viLONDON, Aug. 26, 2025 /PRNewswire/ -- Virax Biolabs Group Limited (NASDAQ: VRAX) ("Virax" or the "Company"), an innovative biotechnology company focused on immune response detection and diagnostics, today announced it has signed a Research Services Agreement ("RSA") with Emory University'sCenter for the Advancement of Diagnostics for a Just Society ("ADJUST Center") to conduct clinical studies of ViraxImmune™. These studies will focus on immune profiling in individuals with post-viral syndromes, beginning with post-acute sequelae of SARS-CoV-2 ("PASC"), commonly known as long COVID..

$VRAX: BOooommmmmmmmm.............. shot up to $1.20

That was a quick $0.40 gainer in Premarket


GO $VRAX

Upcoming Catalysts?

VRAX under $2

$VRAX: Chiner birdflu on the rise again ??????????

This is one of those to keep an eye on if the hype increases.

Now $1.45

GO $VRAX

VRAX.................https://stockcharts.com/h-sc/ui?s=VRAX&p=W&b=5&g=0&id=p86431144783

vrax.......................https://stockcharts.com/h-sc/ui?s=Vrax&p=W&b=5&g=0&id=p86431144783

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vrax...........................https://stockcharts.com/h-sc/ui?s=vrax&p=W&b=5&g=0&id=p86431144783

vrax...............................https://stockcharts.com/h-sc/ui?s=vrax&p=W&b=5&g=0&id=p86431144783

VRAX..........................https://stockcharts.com/h-sc/ui?s=VRAX&p=W&b=5&g=0&id=p86431144783

vrax.........................https://stockcharts.com/h-sc/ui?s=vrax&p=W&b=5&g=0&id=p86431144783

VRAX................................https://stockcharts.com/h-sc/ui?s=VRAX&p=W&b=5&g=0&id=p86431144783

VRAX: Hey, BEST of luck there!! (I wish their PR said ENTIRE British Commonwealth, rather than just Britain & Ireland --- but, likely encompasses ALL of their 'Empire'. And surely YOU know that the Brits control Planet Earth vis-a-vis their Observatory at Greenwich!! "Spring-Forward"; then "Fall-Backward"!! Although a couple US States & a couple Nations claim they don't obey that rule --- in TRUTH, they are merely joking!!!)

im in now, but so much selling, hard to get traction above key 2.80 level

VRAX: Heck, all ya missed was LOSING money!! (I know, your post was conspicuously SARCASTIC!!)

Thx,

missed it

VRAX: This is USA's "Invest-in-America" to the British Empire's Fleet at Jutland --- OPEN FIRE!!!!

VRAX: Reasonable 4-mil. Float --- way LOWER than all of the other bloated-soaring-pigs today. (So I grabbed a 'Starter Lotto Ticket'; God help me!!)

Next resistance $3.46 at )3.10 +88% watch out for GOVX 2.09 they have monkey power also

Holy monkeys $2.90s + 72%

Monkeypox back in favor $2.08 + 23% hod at 1.99. Wait for a pullback can easily fallback to $1.60s support 

VRAX.....................................https://stockcharts.com/h-sc/ui?s=VRAX&p=W&b=5&g=0&id=p86431144783

VRAX 10 day hourly

VRAX...............................https://stockcharts.com/h-sc/ui?s=VRAX&p=W&b=5&g=0&id=p86431144783