Dexcom’s over-the-counter nod sets stage for broader CGM use

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The Food and Drug Administration cleared the first over-the-counter continuous glucose monitor (CGM) on Wednesday, allowing people to buy a new sensor made by Dexcom without a prescription. Dexcom had initially sought to offer its new Stelo device to people with Type 2 diabetes who don’t take insulin, but the FDA expanded on that, opening the CGM to most adults who don’t take insulin. 

The broad indication clears a pathway for Dexcom to grow its CGM business, and for rival Abbott, which plans to bring a wellness-focused sensor to the U.S.

“The indication for use is broad,” said Dexcom Chief Operating Officer Jake Leach. “That covers this population that Stelo was designed for, but it also covers a broader population too. We feel that over time, the opportunity for CGMs to provide benefit to people goes far beyond diabetes.”

Dexcom expects growth as CGMs become more accessible

Stelo is based on the same hardware as Dexcom’s G7 CGM, but the smartphone app that pairs with the device was redesigned to focus on people with Type 2 diabetes who don’t take insulin and want to learn how their glucose changes throughout the day. It’s not meant to be used by people who take insulin or have a history of hypoglycemia, as those alerts are not designed into the device.  

The sensor also has a 15-day wear time, which is five days longer than Dexcom’s other CGMs. Leach said the company ran a clinical study to show its performance and accuracy over 15 days.

Dexcom still plans to debut Stelo in the summer. The company hasn’t yet said where it will sell Stelo or how much it will cost. J.P. Morgan and William Blair analysts expect the device to be priced competitively with Abbott’s Freestyle Libre CGMs, which cost about $80 per month. 

“Over time, we’re going to see expanded go-to-market strategies,” Leach said. “This is a brand new category.” 

He added that expanding Dexcom’s sales team to call more primary care physicians is “definitely part of the puzzle.” The device will also include a feature that allows physicians to review data to see how patients are faring, even though it doesn’t require a prescription. 

William Blair analyst Margaret Kaczor wrote the broad clearance should increase Dexcom’s total addressable market by “many multiples,” adding about 25 million people with Type 2 diabetes who don’t take insulin to the current market of 7.5 million people in the U.S. with diabetes who take insulin. About 98 million adults in the U.S. have prediabetes, according to the Centers for Disease Control and Prevention, and they also could use Stelo under the current indication. 

The over-the-counter label should meaningfully reduce barriers to access, Kaczor wrote. 

“This is important not only for non-insulin users, where demand has been strong despite limited access, but it opens up the non-diabetic market for CGM technologies altogether,” she wrote in a research note on Wednesday. 

Dexcom forecast that Stelo would contribute one percentage point to total company revenue growth this year, or about $40 million. Leach reiterated that projection, adding that “over time, it will be a very important part of our overall portfolio of products because it does serve such a broad segment.” 

BTIG analyst Marie Thibault estimated Dexcom could see a roughly $100 million annual run-rate because of the over-the-counter access, even though the launch date for Stelo remains unchanged.

An oval-shaped device is on a grey patch.

Dexcom’s Stelo CGM has a 15-day wear time and is based on the same hardware as its G7 sensor.

Courtesy of Dexcom

FDA decision sets a ‘high bar’ for competitors

Competitor Abbott is also working to bring its CGM technology to a broader group of people. Last year, the company rolled out a new product called Lingo, which uses CGM technology for general wellness purposes, but it is not intended for people with diabetes.