FDA grants breakthrough status for Alzheimer’s treatment

Nov. 9, 2021

Renew Bioscience said it has received Breakthrough Device Designation status from the U.S. Food and Drug Administration (FDA) for the Cerezen Device, a treatment for mild cognitive impairment due to Alzheimer’s disease and mild dementia of the Alzheimer’s type.

An important risk factor for cognitive impairment and dementia is poor vascular health, with cerebral blood flow and endothelial function believed to play a significant role in vascular health. The Renew Cerezen Device is a drug-free, non-invasive technology, designed to improve cerebral vascular health by enhancing circulation, simulating the physiological effects of vigorous exercise, and stimulating endothelial cell function through a series of treatment sessions.

The Cerezen Device utilizes ECP (External Counterpulsation) therapy that enhances blood flow and overall vascular efficiency. During the therapy, a technician wraps inflatable cuffs (similar to blood pressure cuffs) around the patient’s calves, thighs and hips. The cuffs then synchronize to inflate and deflate between heartbeats. The external counter-pulsation process delivers more oxygenated blood to the body and brain. The process is soothing and relaxing for patients, like a massage. Cerezen must be used under the oversite of a healthcare professional.

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Courtesy of NIAID, NIH
Scanning electron micrograph of Lassa virus budding off a cell. Lassa virus (LASV) is an arenavirus that causes Lassa hemorrhagic fever, a type of viral hemorrhagic fever (VHF) in humans and other primates. NIAID.
Courtesy of Dr. Tomohiro Kaneko from Juntendo University, Japan
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