JERUSALEM, Dec. 19, 2013 (GLOBE NEWSWIRE) -- Brainsway Ltd. (TASE:BRIN) is pleased to announce that the U.S. Food and Drug Administration ("FDA") has approved an Investigational Device Exemption ("IDE") that allows the Company to begin implementing a double-blind, multi-center study to assess the efficacy of the its Deep TMS device in treating patients suffering from obsessive-compulsive disorder ("OCD").
The IDE approval was granted on the basis of the FDA's determination that this is a non-significant risk ("NSR") study. Accordingly, Brainsway intends to act quickly in order to initiate the study following receipt of the requisite Investigational Review Board ("IRB") approvals. Approximately 15 medical centers in the United States, Europe and Israel are expected to participate in the study, which will involve approximately 100 OCD patients. The trial subjects will be divided into two groups: a sham treatment group and a real stimulation treatment group.
About Brainsway
Brainsway develops a medical device for the noninvasive treatment of common brain disorders. The device is based on a uniquely shaped electromagnetic coil connected to a rapidly changing current supply, which produces magnetic fields capable of affecting different areas of the brain. Deep brain areas can be either excited or inhibited, depending on the frequency of the magnetic field.
Forward-Looking Statements
This press release contains forward-looking statements, which reflect the Company's current expectations regarding future events. The forward-looking statements involve risks and uncertainties. Actual events could differ materially from those projected herein. Investors should consult the Company's ongoing quarterly filings and annual reports for additional information on risks and uncertainties relating to these forward-looking statements. The reader is cautioned not to rely on these forward-looking statements. The Company disclaims any obligation to update these forward-looking statements.