Resources
Frequently Asked Questions
Find answers to common questions about Prevena Health, our continuous molecular intelligence platform, disease areas, privacy practices, and partnership opportunities.
About Prevena Health
What is Prevena Health?
Prevena Health is a health technology company building a continuous molecular intelligence platform. The platform is designed to detect subtle biological signals through non-invasive wearable sensing, multiplexed assay cartridges, and a clinician-connected intelligence layer. Prevena Health's goal is to support earlier awareness of disease-related molecular changes. Learn more on our homepage.
What is continuous molecular intelligence?
Continuous molecular intelligence refers to the ongoing, automated measurement and analysis of molecular biomarkers over time, rather than relying on single-point-in-time laboratory tests. Prevena Health's platform is designed to sample interstitial fluid continuously, quantify relevant analytes, and surface trends that may indicate early biological changes.
Is Prevena Health available for purchase?
No. Prevena Health's platform is currently in development and is not commercially available. The company is conducting research and development to validate its technology and biomarker approach. Information on this website is provided for informational purposes only.
Is Prevena Health FDA approved?
No. Prevena Health's platform has not been cleared, approved, or authorized by the U.S. Food and Drug Administration (FDA) or any other regulatory body. The platform is in the research and development phase, and regulatory submissions have not yet been made.
Where is Prevena Health based?
Prevena Health is a U.S.-based health technology company. For inquiries, you can reach the team at contact@prevenahealth.com.
The Platform
How does the Prevena Health platform work?
The Prevena Health platform consists of three integrated components: a skin-worn wearable sensor that continuously samples interstitial fluid, a multiplexed assay cartridge that quantifies multiple biomarkers simultaneously, and a mobile app with an intelligence layer that analyzes trends over time. Together, these components are designed to provide longitudinal molecular data to clinicians and researchers. See the Platform overview for more details.
What is the wearable sensor?
The wearable sensor is a skin-worn device designed to continuously sample interstitial fluid through minimally invasive microneedle technology. It is intended to be comfortable for extended wear and to provide a steady stream of molecular data without requiring traditional blood draws.
What is the assay cartridge?
The assay cartridge is a multiplexed consumable component that quantifies multiple biomarkers from a single interstitial fluid sample. It is designed to detect protein, nucleic acid, and metabolic analytes associated with various disease areas using advanced immunoassay and molecular detection technologies.
How does the mobile app and intelligence layer work?
The mobile app receives biomarker data from the wearable sensor and assay cartridge, then presents longitudinal trends to users and their clinicians. The intelligence layer applies algorithmic analysis to identify meaningful changes in biomarker trajectories, helping to surface signals that may warrant further clinical evaluation.
What is interstitial fluid sensing?
Interstitial fluid (ISF) is the fluid that surrounds cells in body tissues. Research has shown that many clinically relevant biomarkers present in blood are also detectable in ISF. Sensing ISF through microneedle-based wearable technology may offer a less invasive alternative to repeated blood draws for molecular monitoring.
Disease Areas & Biomarkers
What diseases does Prevena Health target?
Prevena Health is investigating biomarkers associated with several major disease areas, including cancer, cardiac disease, stroke, Alzheimer's disease, and neurological injury. The platform is designed to be extensible across multiple conditions where early molecular signals may precede clinical symptoms.
What biomarkers does the platform track?
The platform is being developed to track a range of circulating biomarkers, including high-sensitivity troponin, NT-proBNP, D-dimer, C-reactive protein (CRP), circulating tumor DNA (ctDNA), PSA, neurofilament light chain (NfL), GFAP, phosphorylated tau (p-tau), and others. The specific panel depends on the disease area under investigation.
How is continuous monitoring different from traditional blood tests?
Traditional blood tests provide a single snapshot of biomarker levels at one moment in time. Continuous molecular monitoring, as Prevena Health is developing, aims to track biomarker trajectories over days, weeks, and months. This longitudinal approach may reveal trends, rate-of-change patterns, and subtle shifts that a single test could miss.
Can the platform diagnose disease?
No. Prevena Health's platform is not a diagnostic device and is not intended to diagnose, treat, cure, or prevent any disease. It is being designed as a molecular surveillance tool that surfaces biomarker signals and trends for review by qualified healthcare professionals. Any clinical decisions should be made by a licensed clinician.
What is longitudinal molecular monitoring?
Longitudinal molecular monitoring is the practice of measuring and tracking molecular biomarkers repeatedly over an extended period. By observing how biomarker levels change over time, clinicians and researchers may identify trends that indicate emerging biological changes earlier than periodic single-point testing.
Privacy, Safety & Trust
How does Prevena Health protect patient data?
Prevena Health is committed to protecting personal and health-related data through encryption, access controls, and privacy-by-design principles. The platform is being developed with data security as a foundational requirement. For details, see our Privacy Policy.
Is the platform HIPAA compliant?
Prevena Health is designing its platform and data handling practices with HIPAA compliance requirements in mind. As the platform is still in development, full compliance measures are being built into the architecture from the ground up to ensure readiness for clinical deployment.
Can I use Prevena Health in an emergency?
No. Prevena Health is not an emergency service. The platform and any future alerting features are not substitutes for calling 911 or seeking immediate medical care. If you are experiencing a medical emergency, call emergency services immediately.
Who reviews the data?
Prevena Health's platform is designed to present biomarker data and trends to qualified healthcare professionals, including clinicians and researchers. The platform is intended to support — not replace — clinical judgment. Data interpretation and any resulting medical decisions are the responsibility of licensed healthcare providers.
What clinical validation is being conducted?
Prevena Health is pursuing rigorous clinical validation of its sensing technology, assay performance, and biomarker correlations. The company is committed to evidence-based development and plans to publish research findings and seek appropriate regulatory pathways as the platform matures.
Partnerships
How can clinicians or researchers partner with Prevena Health?
Prevena Health welcomes collaboration with clinicians, researchers, and academic institutions interested in continuous molecular surveillance. To explore partnership opportunities, please contact partners@prevenahealth.com or visit the Partners section of our website.
Is Prevena Health seeking investors?
Prevena Health is open to conversations with aligned investors who share the company's vision for proactive, molecular-level health monitoring. For investment inquiries, please reach out to contact@prevenahealth.com.
Can health systems integrate the platform?
Prevena Health is designing its platform with health system integration in mind, including compatibility with electronic health record (EHR) systems and clinical workflows. As the platform advances through development, the company plans to work with health system partners to ensure seamless integration.
Prevena Health's platform is in development and is not commercially available. It has not been cleared, approved, or authorized by the U.S. Food and Drug Administration (FDA) or any other regulatory body. It is not a diagnostic device. Content on this page is for informational purposes only and does not constitute medical advice, diagnosis, or treatment.
Have more questions?
Reach out to learn more about Prevena Health's platform, research, and partnership opportunities.
Contact Us