Non-invasive neuromodulation therapy for Alzheimer’s with FDA Breakthrough Device Designation
Preserve brain volume in Alzheimer’s patients through daily home treatment; Slow cognitive and functional decline in early-stage Alzheimer’s; Maintain daily function in patients with mild cognitive impairment; Treat patients with abnormal gamma wave activity; Expand to other neurodegenerative diseases
Received FDA Breakthrough Device Designation for Alzheimer’s; Showed significant slowing of disease progression in OVERTURE feasibility study; Expanding to other neurodegenerative diseases; Published at AAIC25; Featured in Bloomberg and Nasdaq interviews; Active clinical study pipeline with HOPE study ongoing