Market Watch | July 23, 2020
FDA Grants Soterix Medical IDE Approval For Home-Based tDCS-LTE Trial For Depression
Soterix Medical Inc. announces it has received Investigational Device Exception (IDE) from the U.S. Food and Drug Administration (FDA) to launch a trial of transcranial Direct Current Stimulation-Limited Total Energy (tDCS-LTE) neuromodulation at-home for individuals with major depressive disorder. Soterix Medical developed proprietary technology supporting reliable home-based tDCS including the single-use SNAPpadâ„¢ electrodes that ensure clean and tolerated therapy at-home, and the ElectraRxâ„¢ digital health care platform that provides caregivers ongoing insight on consumer response and full control of ongoing therapy.
Soterix Medical Inc. was formed to develop and deploy innovative medical treatments . . .
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