San Diego Business Journal

Obalon Therapeutics Announces $75M IPO; Gets FDA Approval

By Brittany Meiling Monday, September 12, 2016
   
Obalon Therapeutics won FDA for its weight-loss pill, a dissolvable capsule that contains a folded gastric balloon. Photo by Obalon Therapeutics

Obalon Therapeutics won FDA for its weight-loss pill, a dissolvable capsule that contains a folded gastric balloon. Photo by Obalon Therapeutics

San Diego’s Obalon Therapeutics Inc. is on a roll. After announcing a $75 million IPO on Friday, the company said this morning that it has received FDA approval of its lead product: the Obalon Balloon System.

Obalon’s weight-loss product is a gastric balloon folded inside a dissolvable capsule (the size of a vitamin pill). The patient swallows the capsule, which is attached to a thin tube called a micro catheter. When the pill reaches the stomach, gas is pumped into the balloon through the tube. Once inflated, the tube is detached and drawn out of the patient’s mouth. The procedure can be done in about five minutes, without anesthesia or sedation.

Obalon’s weight-loss balloon differs from gastric bypass in many ways – most notably its target market.

The candidates for gastric bypass surgery typically have a body mass index of over 40, which is considered “morbidly obese.” Andy Rasdal, founder and chief executive officer of Obalon, said in an interview last year that the company wanted to develop an option for the much larger percentage of the population – people who are clinically obese, but not morbidly so.

“Today, the options are really diet, exercise and surgery,” Rasdal said. “Surgery is only relevant to the morbidly obese people. Our intention was to create a device that has a safety and risk profile that is very benign, so that newly obese people who have clearly failed diet and exercise have another option.”

Starting in 2012 Obalon had sold an earlier version of the weight-loss balloon system in the European Union, Mexico and the Middle East. The company said in the filing that in 2015 it stopped selling outside of the Middle East and focused on earning permission to sell in the U.S.

In the clinical trial that earned the balloon FDA approval, 387 patients in the in the U.S. (across fifteen clinical trial sites) were randomized in a double-blind, sham-controlled study.

The patients in the clinical trial received either three Obalon balloons or three sham placebo-like devices that looked similar to the balloons, but were filled with sugar. The patients in both groups were given minimal diet counseling of 25 minutes every three weeks. About 65 percent of patients who received the Obalon Balloon System experienced “clinically meaningful weight loss” of at least 5 percent of their total body weight, which is twice as many people than in the sham-control group.

The Obalon Balloon System is expected to be available in early 2017 to physicians who complete the Obalon Balloon System training program. Obalon is currently hiring training personnel to ensure that the product can be implemented in the commercial setting with the same results as the clinical trial.

The medical device company’s planned IPO would be the second this year by a San Diego-based company, and the first life science firm to go public in 16 months.

Carmel Valley-based Airgain Inc., which makes antennas for mobile devices and household devices, raised $12 million in August in San Diego’s first initial public offering of the year. Airgain’s offering ended a 15-month IPO drought in San Diego dating back to May 2015, when life science company ATyr Pharma Inc. raised $75 million.