GLP-1 receptor agonists (GLP-1s) continue to dominate headlines, but the conversation has moved beyond diabetes and obesity toward their burgeoning use across a much wider range of conditions.
Employers who invested significant effort in deciding whether to cover GLP-1s for obesity may find that it was only the first of many such decisions they will need to make in the years ahead. They also understand that, as clinical indications expand, waiting and reacting is not a tenable strategy.
For plan sponsors, the story of GLP-1 coverage may ultimately be one of trying to keep up.
From off-label use to front-page news
To understand where GLP-1s are today, consider how they got here. Their runaway success as an off-label treatment for obesity led to broader use in comorbid cardiovascular and metabolic conditions, and that pattern of use preceded a wave of formally approved indications.
Since 2017, the FDA has expanded indications beyond diabetes to include obesity, cardiovascular risk reduction, chronic kidney disease, obstructive sleep apnea, and metabolic dysfunction–associated steatohepatitis (MASH).
GLP-1s’ trajectory from off-label prescribing to clinical trials and FDA approvals has helped catalyze research well beyond the realm of metabolic health.
The next chapter for GLP-1s
Early clinical data suggest that GLP-1s may be uniquely effective in treating substance use disorders because they act directly on the brain’s reward pathways.¹ Fifteen clinical trials are currently underway to test GLP-1s for cocaine, alcohol, tobacco and opioid use disorders.²
GLP-1 receptor agonists’ influence on cue reactivity, craving and impulsivity could have broader implications for psychiatric prescribing. Researchers are actively investigating the efficacy of GLP-1s for other compulsive behaviors, such as gambling and binge eating.
There is also increased focus on using GLP-1s to treat chronic inflammation. Semaglutide, which is sold under brand names including Ozempic and Wegovy, has been associated with roughly a 40 percent reduction in C-reactive protein, and a growing body of evidence suggests that GLP-1s may regulate immune activity rather than simply suppress it.³
Broad public interest has also grown around microdosing GLP-1s for a range of supposed preventative and wellness-related benefits. Evidence for these uses remains limited, but the trend is likely to continue, particularly as access expands and lower-cost options become more widely available.
At present, GLP-1s may appear to be in their “panacea era” as researchers test their potential across an unusually wide range of disease states. The boundaries of what these drugs can and cannot effectively treat will only come into focus over time, but their role in behavioral health and chronic inflammation appears increasingly likely to define the next phase of the GLP-1 story.