The FDA has approved EnteroMedic's VBLOC vagal blocking therapy. Delivered via the ‘Maestro System’, it has been reported to be the first medical device approved for obesity treatment that targets the nerve pathway between the brain and the stomach. The device acts by sending an electrical pulse to block vagal nerve signals involved in controlling feelings of hunger and fullness. The Maestro System is approved for the treatment of adult patients with obesity who have a Body Mass Index (BMI) of at least 35 to 45 kg/m2 with one or more obesity-related health condition and who have failed to lose weight in a supervised weight management program within the past five years.
"This is a novel device that interrupts signals from the stomach to the brain that are believed to be involved with stomach emptying and feelings of fullness," said Martin Binks, PhD, FTOS, Secretary/Treasurer of The Obesity Society (TOS) and Associate Professor of Nutritional Sciences at Texas Tech University. "In clinical trials the device resulted in a clinically meaningful weight loss of 8.5% after one year and the FDA determined this was an appropriate risk-benefit profile to approve the device for clinical use."
The FDA has requested the company collect additional safety and efficacy data over five years.
"We're encouraged that FDA is willing to continue to consider adding important and innovative new options to the treatment toolbox," said Dr. Binks. "In addition to the five FDA-approved anti-obesity drugs now available, these novel treatment options can give additional choices to individuals with obesity who have found little success with diet and exercise alone. Medical devices can be part of comprehensive, individualised obesity treatment plan for some patients. For the first time in history, we see a glimpse of the future for obesity treatment – the potential to treat the disease with a full spectrum of tools.”