Xlife Sciences AG Delivers Breakthrough in Early Alzheimer’s Detection, Unlocking Major Market Opportunity
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This press release is provided in English and German. Xlife Sciences AG Delivers Breakthrough in Early Alzheimer’s Detection, Unlocking Major Market Opportunity ZURICH, Switzerland, December 01, 2025 / Biotech Newswire / -- Xlife Sciences AG (SIX: XLS), together with saniva diagnostics GmbH, today announced a landmark achievement: NeuroMex is the world’s first certified and clinically validated medical device for early detection of Alzheimer’s disease based on the recording of motor responsiveness. It has now successfully completed pivotal clinical trials following FDA (513g) and MDR (CE) certification. NeuroMex delivers 83.5% accuracy in identifying early-stage Alzheimer’s without traditional cognitive tests, enabling rapid, scalable preventive screening. With the device now entering the partnering phase, it is poised to become a standard component of annual health examinations, opening significant revenue streams and strategic partnership opportunities in healthcare and pharmaceuticals. "NeuroMex transforms early detection, allowing timely interventions and optimized resource use in healthcare," said Jenny Nisser, Managing Director of saniva diagnostics GmbH. By combining breakthrough science, regulatory approval, and clinical validation, Xlife Sciences is uniquely positioned to drive adoption, accelerate partnerships, and deliver meaningful impact for patients, healthcare systems, and investors.
Semantical keywords: Alzheimer Disease, Equipment and Supplies, Delivery of Health Care, Xlife Sciences AG, saniva diagnostics GmbH, NeuroMex, early Alzheimer’s detection, medical device, motor responsiveness, pivotal clinical trials, FDA 513g, CE certification, early-stage Alzheimer’s, preventive screening, partnering phase, healthcare, pharmaceuticals, Jenny Nisser, Oliver R. Baumann, neurodegenerative diagnostics, preventative care
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