Mounjaro Beats Ozempic, So Why Isn't It More Popular?

Effectiveness isn't the only factor determining choice of GLP-1 receptor agonist for weight loss.
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-TRANSCRIPT-
Welcome to Impact Factor, your weekly dose of commentary on a new medical study. I'm Dr F. Perry Wilson of the Yale School of Medicine.
It's July, which means our hospital is filled with new interns, residents, and fellows all eager to embark on a new stage of their career. It's an exciting time - a bit of a scary time - but it's also the time when the medical strategies I've been taking for granted get called into question. At this point in the year, I tend to get a lot of "why" questions. Why did you order that test? Why did you suspect that diagnosis? Why did you choose that medication?
Meds are the hardest, I find. Sure, I can explain that I prescribed a glucagon-like peptide 1 (GLP-1) receptor agonist because the patient had diabetes and was overweight, and multiple studies show that this class of drug leads to weight loss and reduced mortality risk. But then I get the follow-up: Sure, but why THAT GLP-1 drug? Why did you pick semaglutide (Ozempic) over tirzepatide (Mounjaro)?
Here's where I run out of good answers. Sometimes I choose a drug because that's what the patient's insurance has on their formulary. Sometimes it's because it's cheaper in general. Sometimes, it's just force of habit. I know the correct dose, I have experience with the side effects - it's comfortable.
What I can't say is that I have solid evidence that one drug is superior to another, say from a randomized trial of semaglutide vs tirzepatide. I don't have that evidence because that trial has never happened and, as I'll explain in a minute, may never happen at all.
But we might have the next best thing. And the results may surprise you.
Why don't we see more head-to-head trials of competitor drugs? The answer is pretty simple, honestly: risk management. For drugs that are on patent, like the GLP-1s, conducting a trial without the buy-in of the pharmaceutical company is simply too expensive - we can't run a trial unless someone provides the drug for free. That gives the companies a lot of say in what trials get done, and it seems that most pharma companies have reached the same conclusion: A head-to-head trial is too risky. Be happy with the market share you have, and try to nibble away at the edges through good old-fashioned marketing.
But if you look at the data that are out there, you might wonder why Ozempic is the market leader. I mean, sure, it's a heck of a weight loss drug. But the weight loss in the trials of Mounjaro was actually a bit higher. It's worth noting here that tirzepatide (Mounjaro) is not just a GLP-1 receptor agonist; it is also a gastric inhibitory polypeptide agonist.
photo of Weight Loss, GLP-1
But it's very hard to compare the results of a trial pitting Ozempic against placebo with a totally different trial pitting Mounjaro against placebo. You can always argue that the patients studied were just too different at baseline - an apples and oranges situation.
Newly published this week, a study appearing in JAMA Internal Medicine uses real-world data and propensity-score matching to turn oranges back into apples. I'll walk you through it.
The data and analysis here come from Truveta, a collective of various US healthcare systems that share a broad swath of electronic health record data. Researchers identified 41,222 adults with overweight or obesity who were prescribed semaglutide or tirzepatide between May 2022 and September 2023.
You'd be tempted to just see which group lost more weight over time, but that is the apples and oranges problem. People prescribed Mounjaro were different from people who were prescribed Ozempic. There are a variety of factors to look at here, but the vibe is that the Mounjaro group seems healthier at baseline. They were younger and had less kidney disease, less hypertension, and less hyperlipidemia. They had higher incomes and were more likely to be White. They were also dramatically less likely to have diabetes.
To account for this, the researchers used a statistical technique called propensity-score matching. Briefly, you create a model based on a variety of patient factors to predict who would be prescribed Ozempic and who would be prescribed Mounjaro. You then identify pairs of patients with similar probability (or propensity) of receiving, say, Ozempic, where one member of the pair got Ozempic and one got Mounjaro. Any unmatched individuals simply get dropped from the analysis.
Transcript in its entirety can be found by clicking here: www.staging.me...