NeuroEM Therapeutics Unveils Results Of Early Stage Study On TEMT For Alzheimer’s

NeuroEM Therapeutics, a clinical stage medical device company, has released results from an early stage study that assessed safety and initial efficacy of transcranial electromagnetic treatment (TEMT) using its investigational MemorEM head device for Alzheimer’s disease (AD).

The pilot study was a single centre, single arm trial involving eight patients 63 years of age and older with mild to moderate AD.\

The two-month trial evaluated the safety and initial efficacy of TEMT, and the results showed that that TEMT is safe in all eight participating patients with mild to moderate AD and enhanced cognitive performance in seven of them, as measured by standard cognition scales.

NeuroEM Therapeutics CEO Gary Arendash said: “This pioneering study suggests that TEMT may be an entirely new therapeutic intervention against Alzheimer’s disease. Our bioengineering technology may be succeeding where drug therapy against this devastating disease has thus far failed.

“TEMT appears to be affecting the Alzheimer’s disease process through several actions directly inside neurons (brain cells), which is where we believe the disease process needs to be stopped and hopefully reversed.”

The study was published in the Journal of Alzheimer’s Disease.

AD is a progressive and mortal brain disorder caused by the damage or destruction of brain cells (neurons) in parts of the brain that control thinking, learning and memory, and leads to memory loss, language problems and other serious symptoms.

People with AD tend to become more limited in performing daily activities over time and eventually become bed-bound, needing full-time care. – NS Medical Devices