PathMaker Neurosystems Announces Completion of Pivotal European Clinical Trial Evaluating MyoRegulator® for the Non-Invasive Treatment of Post-Stroke Spasticity
Retrieved on:
Monday, September 27, 2021
Clinical trial, MTS, Stroke, Queensland Brain Institute, Health, Amyotrophic lateral sclerosis, FDA, IRB, Institute, Spasticity, Patient, APHP, NSR, Disability, Connective tissue disease, Station F, Heart, GLOBE, US Foods, Food and Drug Administration, Cerebral palsy, CNRS, Neurotoxin, Multiple sclerosis, ALS, Brain, ICM, Safety, INSERM, Traumatic brain injury, Sorbonne University, Lists of diseases, Pharmaceutical industry, Medical device
This clinical trial was conducted at the Paris Brain Institute (ICM) in the Piti-Salptrire Hospital in Paris, France and was sponsored by INSERM.
Key Points:
- This clinical trial was conducted at the Paris Brain Institute (ICM) in the Piti-Salptrire Hospital in Paris, France and was sponsored by INSERM.
- We are pleased to have completed this clinical trial to evaluate our MyoRegulator device, commented Nader Yaghoubi, M.D., Ph.D., President and Chief Executive Officer of PathMaker.
- Completion of this trial is an important step in advancing this product as a novel approach to the treatment of spasticity that does not require injected neurotoxins or sedating pharmaceuticals.
- MyoRegulator will be the worlds first non-invasive neuromodulation device for the treatment for muscle spasticity, and will enable the treatment of patients without the need for drugs or surgery.