Salute e Benessere
Newronika Receives Investigational Device Exemption (IDE) from FDA to Initiate U.S. Clinical Trial of Adaptive DBS System
said Dr. Lorenzo Rossi , Co-Founder and CEO of Newronika.
By using real-time feedback from patients' brain signals, Newronika's adaptive DBS solution ensures that therapy is continuously optimized. This patient-tailored approach has the potential to greatly improve outcomes and reduce side effects compared with traditional DBS systems. The company's core mission—to move neurotechnology beyond the current state of the art—remains at the forefront as it advances toward commercial adoption in Europe , the United States , and beyond.
d Prof. Dr. Med. Jens Volkmann , Principal Investigator of the study.
The pivotal trial, involving leading U.S. and international clinical centers, will compare the performance of adaptive DBS against conventional DBS in patients with advanced Parkinson's disease. The results will be pivotal in securing regulatory approval for AlphaDBS in the U.S..
Newronika is transforming deep brain stimulation (DBS) through its adaptive platform that uses real-time patient data to optimize therapy. Founded as a spin-off of the University of Milan and Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico and headquartered in Milan, Italy , the company is committed to advancing neuromodulation beyond conventional limitations. With ongoing research collaborations and now an Investigational Device Exemption from the FDA, Newronika stands at the forefront of next-generation therapeutic innovation for neurological disorders.
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