
Caris Life Sciences Announces New Study Demonstrating the Power and Clinical Utility of its Caris Assure® Blood-Based Assay for Multi-Cancer Early Detection, Minimal Residual Disease and Therapy Selec
IRVING, Texas, July 8, 2025 /PRNewswire/ — Caris Life Sciences® (NASDAQ: CAI), a leading, patient-centric, next-generation AI TechBio company and precision medicine pioneer, announced a landmark study published in Scientific Reports, a Nature journal, demonstrating the accuracy and clinical utility of the Caris Assure® blood-based biopsy assay across the cancer continuum.
The Caris Assure® platform is a breakthrough single assay that combines comprehensive, highly sophisticated molecular profiling of all 23,000+ genes across DNA and RNA in plasma, setting a new blood-based testing standard and revolutionizing management of the cancer care journey. Additionally, Caris sequences DNA in the 'buffy coat,' the layer of centrifuged blood between the red blood cells and plasma, which contains white blood cells and platelets. Caris Assure combines Whole Exome Sequencing (WES) and Whole Transcriptome Sequencing (WTS) with advanced machine learning on a single platform. Caris Assure® is currently used for therapy selection and is capable of enabling accurate early detection and highly sensitive disease monitoring.
'We designed Caris Assure® to be more than a liquid biopsy test. This assay takes advantage of advanced sequencing and computing technology to capture genetic information available from the whole exome and whole transcriptome from the tumor material circulating in the blood and DNA from the patient's white blood cells,' said David Spetzler, MS, PhD, MBA, President of Caris. 'This enables us to provide a very comprehensive individualized picture of a patient's specific disease state. This is the first time so much molecular information has been available from a single blood test, allowing for increased accuracy and additional insights to inform physicians in helping to make cancer care decisions.'
The Caris Assure® liquid biopsy platform, powered by the Assure Blood-based Cancer Detection AI (ABCDai), was trained on over 376,000 whole exome and whole transcriptome tissue profiles and over 7,000 matched blood and tissue samples. In addition to therapy selection, the study validates the performance of Caris Assure® in:
Multi-Cancer Early Detection (MCED): Achieved sensitivities of 83.1% to 95.7% across cancer stages I–IV at 99.6% specificity.
Diagnostic Pathway Predictor: Accurately identified the diagnostic pathway for MCED-positive cancers using the ABCDai-GPS model.
MRD and Recurrence Monitoring: Demonstrated significant predictive power for recurrence, with hazard ratios of 33.4 (p < 0.005) for MRD and 4.39 (p = 0.008) for therapeutic monitoring.
Caris Assure® does not require a prior tissue biopsy. Instead, its AI model identifies tumor-derived signals based on patterns learned from hundreds of thousands of tumors. This enables a tissue-agnostic, highly sensitive approach to cancer detection and monitoring.
While Caris Assure® is currently commercially available for therapy selection in advanced cancers, this study lays the groundwork for expanding into early detection, MRD and therapeutic monitoring. Caris is actively pursuing reimbursement and regulatory pathways to bring these applications to market.
'This is more than a validation study; it is a blueprint for the future of cancer diagnostics,' added Spetzler. 'Our goal is to create a seamless ecosystem where patients and clinicians can rely on one platform throughout the entire cancer journey.'
About Caris Life Sciences Caris Life Sciences® (Caris) is a leading, patient-centric, next-generation AI TechBio company and precision medicine pioneer that is actively developing and commercializing innovative solutions to transform healthcare. Through comprehensive molecular profiling (Whole Exome and Whole Transcriptome Sequencing) and the application of advanced AI and machine learning algorithms at scale, Caris has created the large-scale, multimodal clinico-genomic database and computing capability needed to analyze and further unravel the molecular complexity of disease. This convergence of next-generation sequencing, AI and machine learning technologies, and high-performance computing provides a differentiated platform to develop the latest generation of advanced precision medicine diagnostic solutions for early detection, diagnosis, monitoring, therapy selection and drug development.
Caris was founded with the belief and vision that combining a vast set of consistently generated molecular information with robust data-driven insights could realize the potential of precision medicine for patients. Headquartered in Irving, Texas, Caris has offices in Phoenix, New York, Cambridge (MA), Tokyo, Japan and Basel, Switzerland. Caris or its distributor partners provide services in the U.S. and other international markets.
The Scientific Report study is available on CarisLifeSciences.com.
Forward Looking Statements:This press release contains forward-looking statements, within the meaning of the federal securities laws, about Caris Life Sciences and its business. Statements about the performance and accuracy of Caris Assure discussed in this press release are based on testing and analysis to date, as reflected in the publication discussed, and future results and performance may differ materially from these findings. All statements other than statements of historical facts contained in this press release are forward-looking statements. In some cases forward-looking statements can be identified by words such as 'may,' 'will,' 'should,' 'would,' 'expect,' 'plan,' 'anticipate,' 'could,' 'intend,' 'target,' 'project,' 'potential,' 'contemplate,' 'believe,' 'estimate,' 'predict,' 'potential' or 'continue' or similar expressions.
You should not rely upon forward-looking statements as predictions of future events. Although we believe that the expectations reflected in these forward-looking statements are reasonable based on information currently available to us, we cannot guarantee that the future results, discoveries, levels of activity, performance or events and circumstances reflected in forward-looking statements will be achieved or occur. Forward-looking statements involve known and unknown risks and uncertainties, some of which are beyond our control. Risks and uncertainties that could cause our actual results to differ materially from those indicated or implied by the forward-looking statements in this press release include, among other things: developments in the precision oncology industry; future financial performance, results of operations or other operational results or metrics; development, validation and timing of future solutions; the rapidly evolving competitive environment in which we operate; third-party payer reimbursement and coverage decisions; our ability to protect and enhance our intellectual property; regulatory requirements, decisions or approvals (including the timing and conditions thereof) related to our solutions; our compliance with laws and regulations; and our ability to hire and retain key personnel as well as risks, uncertainties, and other factors described in the section titled 'Risk Factors' and elsewhere in the prospectus for our initial public offering filed with the Securities and Exchange Commission on June 20, 2025, and in our other filings we make with the SEC from time to time. We undertake no obligation to update any forward-looking statements to reflect changes in events, circumstances or our beliefs after the date of this press release, except as required by law.
Caris Life Sciences Media: Corporate CommunicationsCorpComm@CarisLS.com214.294.5606
Investor Relations:Narendra ChokshiSenior Vice President, Corporate Developmentnchokshi@carisls.com917.689.3511
Hashtags

Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles


Malaysian Reserve
8 hours ago
- Malaysian Reserve
Geri Care opens its 10th facility at Velachery: state-of-the-art Assisted Living for Elders with India's First Dialysis Day Care Centre
CHENNAI, India, Aug. 20, 2025 /PRNewswire/ — Geri Care, India's pioneer in integrated eldercare, today announced the inauguration of its newest Assisted Living facility in Velachery, Chennai. This milestone marks Geri Care's 10th facility since inception in 2018, a testament to the organisation's rapid growth and unwavering dedication to transforming eldercare in India. This newest 75-bed, state-of-the-art Assisted Living facility is designed for elders requiring expert medical care, including post-surgery recovery, chronic condition management, dementia care, and post-hospitalisation support. As part of this centre, Geri Care is introducing India's first Dialysis Day-care Centre for Elders that will spare families the strain of late-night treatments. Located in close proximity to the Geri Care Hospital, the facility also features a dedicated Elder Fitness Studio for physiotherapy and rehabilitation, along with beautifully landscaped Elder Grove spaces that encourage connection, relaxation, and rejuvenation for residents. The facility was inaugurated by National Award-winning actor, acclaimed filmmaker, and philanthropist, Ms. Suhasini Maniratnam, whose unwavering commitment to social causes extends to championing dignified eldercare, and Padma Shri Prof. Dr. V.S. Natarajan, widely regarded as the 'Father of Geriatric Medicine in India' and a pioneer in shaping the country's approach to senior healthcare. Speaking on the occasion, Dr. Lakshmipathy Ramesh, Founder & Managing Director of Geri Care Health Services said, 'This is a proud milestone for Geri Care. The launch of our state-of-the-art Assisted Living facility is where our vision meets the growing healthcare needs of India's elders. With over 10% of our population aged 60 and above, projected to nearly double by 2050; the demand for specialised eldercare has never been greater.' He added, 'Our 10th facility at Velachery is designed to set new benchmarks. Our dialysis day-care centre, geriatric clinic, elder fitness studio, and physiotherapy services are all open to elders in the neighbourhood. Every detail serves one purpose -to make life healthier, easier, and more dignified. At Geri Care, our mission goes beyond healthcare; it's about giving elders a place where they feel cared for, respected, and valued every day.' Inaugurating the facility, the Chief Guest, Ms. Suhasini Maniratnam said, 'Eldercare is a cause close to my heart, and Geri Care's work shows what true compassion in healthcare looks like. This facility is not just about medical support; it's about dignity, comfort, and giving our elders the quality of life they deserve.' Guest of Honour, Padma Shri Prof. Dr. V.S. Natarajan in his inaugural remarks said, 'Specialised geriatric care is the need of the hour in our ageing nation. Geri Care's 360 degree approach is a model for the future, blending medical excellence with genuine respect for the elderly.' About Geri Care: Founded in 2018 by renowned geriatricians Dr. Lakshmipathy Ramesh & Dr. V. Srinivas, Geri Care is India's first integrated healthcare network exclusively serving senior citizens. Its comprehensive ecosystem spans personalized Home Care, Hospital Services, Assisted Living Centres, and Specialty Geriatric Clinics. Geri Care operates India's first multi-specialty hospitals dedicated to seniors and currently serves over 50,000 elders across multiple cities. To learn more, visit Photo:


Malaysian Reserve
15 hours ago
- Malaysian Reserve
Monument Therapeutics Announces Partnership with Foundation for the National Institutes of Health for Clinical Trial of MT1988, a Novel Treatment for Schizophrenia
MANCHESTER, England, Aug. 19, 2025 /PRNewswire/ — Monument Therapeutics, a stratified medicine company, today announced a partnership with the Foundation for the National Institutes of Health (FNIH) to evaluate MT1988, a novel treatment in development for cognitive impairment associated with schizophrenia, in a proof of principle clinical trial. Schizophrenia is a severe mental health disorder and ranks among the top 15 leading causes of disability worldwide. It is characterized by a range of symptoms, including auditory and visual hallucinations, delusions, and cognitive impairments that affect attention, memory, reasoning, and processing speed. Many individuals begin to show signs of schizophrenia months or even years before receiving a diagnosis. This period, referred to as the 'clinical high risk' (CHR) phase, is currently without effective treatment options, despite its profound impact on functioning and quality of life. This Investigational New Drug (IND)-opening clinical trial for MT1988 is the first patient trial from Monument's precision medicine pipeline. The randomized, placebo-controlled study will enroll 150 CHR participants, who will receive one of two dose levels of MT1988 or placebo over an eight-week treatment period. The trial is on track to begin dosing in the autumn of 2025. The study will evaluate the potential of MT1988 to improve cognitive symptoms in CHR individuals, incorporating a range of clinical and cognitive biomarkers including Monument's proprietary digital biomarker. This approach is designed to assess not only therapeutic effects but also the potential of these biomarkers to predict and monitor treatment response. The trial is part of the FNIH-managed Accelerating Medicines Partnership® Schizophrenia (AMP® SCZ) program, a public-private partnership between the National Institutes Health (NIH) and private sector organizations, including major pharmaceutical companies and nonprofit groups. The program seeks to accelerate the development of more effective treatments for schizophrenia and related mental health conditions. It is supported by NIH grants awarded by the National Institute of Mental Health (NIMH) to Yale School of Medicine (U01MH137298) and Brigham and Women's Hospital (U24MH137171), representing a $44 million investment so far. The clinical trial with MT1988 will be co-led by Dr. Scott Woods and Dr. Youngsun Cho from Yale School of Medicine, Dr. Carrie Bearden from University of California, Los Angeles (UCLA), Dr. John Kane from Northwell Health, Dr. Martha Shenton and Dr. Ofer Pasternak from Brigham and Women's Hospital, Dr. Sylvain Bouix from École de technologie supérieure, Université du Québec, and Dr. Rene Kahn from Icahn School of Medicine at Mount Sinai. This distinguished team brings together diverse expertise across psychiatry, neuroscience, and data science, highlighting a unified commitment to advancing early intervention for schizophrenia. Dr. Kiri Granger, Chief Scientific Officer of Monument Therapeutics, commented: 'This trial marks an exciting milestone for Monument to evaluate MT1988 in a patient population with our proprietary digital biomarker. Studying individuals at clinical high risk allows us to explore early cognitive changes and support the advancement of personalised treatment approaches in early-stage illness. We are thrilled to partner with FNIH and leading investigators on a study that represents a major step forward in developing meaningful treatment options for people at risk of schizophrenia.' About Monument Therapeutics: Monument Therapeutics is a neuroscience-focused drug development company headquartered in Manchester, UK. It applies a unique novel drug development strategy, leveraging digital assessments of cognition to select patients suitable for treatment with new innovative drugs. For more information, please visit About the Foundation for the National Institutes of Health: The Foundation for the National Institutes of Health (FNIH) builds public-private partnerships that connect leading biomedical scientists at the National Institutes of Health (NIH) with their counterparts in life sciences companies, academia, patient organizations, foundations, and regulatory agencies (including the U.S. Food and Drug Administration and European Medicines Agency). Through team science, the FNIH solves complex health challenges and accelerates breakthroughs for patients, regardless of who they are or what health threats they face. The FNIH contributes to the development of new therapies, diagnostics, and potential cures; advances global health; and helps train the next generations of scientists. Established by Congress in 1990 to support the mission of the NIH, the FNIH is a not-for-profit 501(c)(3) charitable organization. For more information about the FNIH, please visit About the Accelerating Medicines Partnership®: Launched in 2014 and managed by the FNIH, the Accelerating Medicines Partnership (AMP) program brings together the National Institutes of Health, U.S. Food and Drug Administration, biomedical and life sciences companies, nonprofits, patient-focused groups, and other organizations to transform the current model for developing new diagnostics and treatments. Using cutting-edge scientific approaches and broad sharing of research data, all AMPs seek to improve understanding of disease pathways, facilitate better selection of targets for drug development, and streamline processes for bringing new treatments to patients. To learn more about AMP, visit For further information, contact: Jenny Barnett, CEO E: jbarnett@ Media inquiries: Christopher Koddermann Tel: +41 (79) 434 25 78 E-mail: chris@ Logo –


Malaysian Reserve
15 hours ago
- Malaysian Reserve
Selonterra announces grant of United States patent on original discoveries in Alzheimer's disease
SAN MATEO, Calif., Aug. 19, 2025 /PRNewswire/ — Selonterra, Inc. ( a biotechnology company developing transformative therapies for neurodegenerative disorders announces that the U.S. Patent and Trademark Office (USPTO) has granted the U.S. Patent No. 12,385,093 entitled 'Use of APOE4 motif-mediated genes for diagnosis and treatment of Alzheimer's disease'. Selonterra focuses on neurodegenerative disorders with strong genetic links, including Alzheimer's disease (AD). APOE4 is the most important genetic factor associated with late onset AD. We discovered that the single nucleotide change in APOE4 regulates the expression of genes in its chromosomal vicinity. These APOE4-motif mediated genes offer novel unexploited targets for the development of small molecule therapeutics for AD. 'We relentlessly pursue intellectual property coverage along the entire development path from our early discoveries, through novel targets to small molecule composition of matter patents,' said Roman Urfer, PhD, Founder and CEO of Selonterra. 'The issuance of our patent around our newly discovered function of the APOE4 single nucleotide polymorphism is testament to our innovative strength,' said Anne Urfer-Buchwalder, PhD, Founder and President of Selonterra. 'These discoveries enable us to exploit the well-established APOE4 root cause of AD from a previously unappreciated angle.' About Selonterra, Inc. Selonterra, Inc. ( pursues transformative approaches to the development of therapies of neurodegenerative disorders, Alzheimer's disease, Parkinson's disease and amyotrophic lateral sclerosis. We harness human genetics, molecular pathway analysis and gene regulatory networks to identify proprietary disease-causing mechanisms and molecular targets, and exploit these to discover effective therapeutics. Selonterra's founders and advisors are scientists and executives with decades of biotech and pharma experience complemented by a global network of collaborator companies. Investor and Media Contact: T: (+1) 650 206 7025E: admin@