The U.S. Food and Drug Administration has given the thumbs up to St. Jude Medical (NYSE:STJ) that allows the Minnesota medical device maker to expand a clinical study of a deep brain stimulation device to treat major depressive disorder.
St. Jude announced Monday that the Broaden severe depression study that is testing its Libra investigational device will now be conducted at 20 medical centers with a total of 125 patients. Before the FDA approval, the study was being conducted at three centers in Chicago, New York and Dallas.