
Healthy Returns: Novo Nordisk's Wegovy deal with CVS won't derail Eli Lilly's obesity market dominance
A version of this article first appeared in CNBC's Healthy Returns newsletter, which brings the latest health-care news straight to your inbox. Subscribe here to receive future editions.
Despite last week's investor jitters, Eli Lilly is far from losing its strong grip on the booming weight loss market.
Here's a recap of what sparked the panic on Thursday if you missed it: CVS Health 's pharmacy benefit manager Caremark said it will prioritize Novo Nordisk 's Wegovy on its standard formularies on July 1, making that weekly injection the preferred GLP-1 drug for obesity.
As part of the move, Caremark will also drop Eli Lilly's weight loss drug Zepbound from those formularies, which represent tens of millions of patients. Caremark negotiated an undisclosed lower net price for Wegovy over Zepbound on its standard formularies, offering savings on Novo Nordisk's drug to clients that opt into those plans.
But employers and unions will ultimately determine how much of those savings on Wegovy get shared with members, CVS said.
Wegovy's list price before insurance is $1,349 for a month's supply, while Zepbound's is $1,086.
That decision by one of the nation's largest PBMs triggered fears of a price war in the weight loss drug market and concerns that Zepbound's sales momentum could stall. Shares of Eli Lilly plunged 11% on Thursday.
But several Wall Street analysts said the selloff was overblown.
"In our view, the Novo/CVS deal does not represent the beginning of an obesity pricing war between Lilly & Novo," BMO Capital Markets analyst Evan Seigerman said in a note on Thursday. He added that in discussions with the companies, both Lilly and Novo emphasized they want to expand patient access – not undercut each other on price.
That may be reassuring to investors worried that a price war could hurt profit margins. But the high list price of those weight loss drugs may remain a major barrier for many patients, particularly those whose health plans don't cover the medications.
Eli Lilly told the firm it is not interested in exclusive "one-of-one" deals with PBMs, while Novo Nordisk said CVS approached the drugmaker about the Wegovy agreement, according to Seigerman.
On an earnings call on Thursday, Eli Lilly CEO David Ricks said the company has been trying to move away from setting high list prices and paying bigger rebates to PBMs for preferential coverage. Instead, Eli Lilly is trying to set list prices closer to what it expects the plans to pay for its drugs.
"We have been very vocal about trying to move away from that," Ricks said, referring to deep PBM rebates.
He added that Zepbound is still growing market share.
Seigerman agreed, saying that Eli Lilly is "continuing to perform where it matters." Zepbound and the company's diabetes drug Mounjaro now make up over half of U.S. GLP-1 prescriptions, outpacing the combined 46% share of Novo Nordisk's Wegovy and its diabetes treatment Ozempic, according to Seigerman.
That "market-share traction clearly demonstrates that physicians and patients prefer Zepbound" over Wegovy, Bernstein analyst Courtney Breen wrote in a separate note on Thursday.
It's unclear how much the CVS formulary change will appeal to employers, especially given that Zepbound is known to be more effective at promoting weight loss than Wegovy. Some patients on the standard formularies may also try to stay on their current Zepbound prescriptions by requesting exemptions, JPMorgan analyst Chris Schott said in a Thursday note.
Eli Lilly's Ricks also said CVS' move mainly affects smaller employers, who are more likely to stick with Caremark's standard formularies. Larger companies covering more patients often use customized formularies, meaning they can still decide to include Zepbound.
Regardless, the CVS-Wegovy deal overshadowed an overall strong quarter for Eli Lilly.
The company's first-quarter revenue and earnings topped estimates on skyrocketing demand for Zepbound and Mounjaro, both of which raked in billions of dollars in sales for the period.
We'll continue to track Eli Lilly's performance in the weight loss drug market, so stay tuned!
Feel free to send any tips, suggestions, story ideas and data to Annika at annikakim.constantino@nbcuni.com.
Health-care marketplace Zocdoc has launched an artificial intelligence phone assistant that can help patients schedule appointments using conversational language.
ZocDoc, founded in 2007, helps connect patients to in-network doctors and book appointments for both in person and virtual care. The company's new AI assistant, called Zo, can handle "unlimited" inbound calls at any hour of the day, eliminating hold times, ZocDoc said in a release.
The company said Zo can save staffers time and improve patients' experiences, which can ultimately encourage them to seek out the care they need. The assistant also serves as a major step toward what the company called its goal of aiding scheduling "everywhere patients are seeking care."
"What's most exciting about Zo is that it is powered by nearly two decades of Zocdoc's expertise in facilitating patient-provider interactions, understanding complex healthcare scheduling logic, and integrating with a broad base of [electronic health records]," Zocdoc CEO Oliver Kharraz said in a statement.
Patients can ask Zo questions like, "Do you take my insurance?," or "Do you have any offices near the West Village?," according to a pre-recorded demo.
Health-care organizations can implement Zo without any upfront fees, long-term costs or commitments, and they don't have to be Zocdoc Marketplace customers, the company said. Providers can try out the assistant for $2 per booked appointment, but organizations that want to roll it out on a larger scale can access discounted pricing.
Zocdoc said early adopters of Zo have been able to resolve up to 70% of all scheduling calls without staff intervention. The average call lasts around two minutes and 30 seconds.
While appointment management is Zo's first use case, Zocdoc said it's exploring other applications for the assistant, including prescription refills, messaging and outbound calls like appointment reminders or last-minute openings.
Read the full announcement here.
Feel free to send any tips, suggestions, story ideas and data to Ashley at ashley.capoot@nbcuni.com.
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Fast Company
11 hours ago
- Fast Company
Weighing the truth: weight management treatments in the age of social media
People turn to social media for information on fashion, finance, product reviews—and now medical advice. This has been particularly true with weight management treatments, including glucagon-like peptide-1 medications, known as GLP-1s, which are frequently hyped on social media. This rise in popularity has led to an influx of misleading information to sell knockoff versions of GLP-1 medicines—ones that aren't approved by the Food and Drug Administration (FDA)—under the pretext of doctor trust and affordability. Misinformation can pose dangerous health risks. Recently, Novo Nordisk, a global pharmaceutical company that has invested 20 years of research into the treatment of obesity as a chronic disease, sponsored a panel at the Fast CompanyGrill during SXSW to discuss this troubling trend. Here are three takeaways from the conversation. (Some quotes have been edited for length and clarity.) 1. Misinformation is on the rise. There is a huge amount of interest from the public around GLP-1s. GLP-1s mimic a naturally occurring hormone produced in the intestines that helps regulate blood sugar levels and appetite. The effectiveness of these drugs has been remarkable for patients managing type 2 diabetes and obesity. Yet, misleading information online may lead to improper use in patients for whom the treatment is not appropriate or the use of illegitimate compounded versions of GLP-1s. Compounded products do not undergo the same review for effectiveness, safety, or quality as FDA approved medicines/drugs and may expose patients to unknown health risks. 2. Compounded medicines are a potential health risk. Compounding's original intent is to tailor medications for individuals with specific needs who cannot use FDA-approved versions. With the FDA's announcement that the shortage of certain GLP-1 medicines has resolved, making or selling knockoff compounded drugs is now illegal under U.S. compounding laws, except in rare circumstances. Concerns about compounded weight management products abound. 'Compounded medications don't go through clinical trial programs, and they're not approved by the FDA,' said Negelle Morris, senior vice president at Novo Nordisk. 'In fact, we've tested quite a number of samples from compounding companies and found impurities—some of them included ingredients on the FDA banned list for use in compounding.' The conversation between patients and healthcare professionals is crucial for effective treatment and care. 'Always tell your healthcare provider what you're doing,' Horn said. 'Even if compounded medication is something I will never give them, if they chose it, I need to know.' 3. Patient safety and care needs to be a top priority. Treating obesity and other chronic illnesses is an ongoing process. 'I think the hardest thing is that this is a journey and it takes work,' said Lisa S., a patient advocate on the panel. Morris echoed this sentiment. 'Any disease that you treat, you are making a long-term commitment,' she said. No one should have to compromise their health due to misinformation or lack of understanding. For this reason, it's important that people find a doctor who can serve as a guide and partner on their weight management journey. 'Healthcare is shared decision-making,' Horn asserted. 'It's not for me to tell my patient what to do, but it's for me to share with them the things that I know, talk to them, and give them as much information as I can.'
Yahoo
14 hours ago
- Yahoo
Can Mounjaro and Zepbound Drive Another Strong Quarter for Eli Lilly?
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USA Today
16 hours ago
- USA Today
MIRA Reports Clear Reversal of Anxiety-Related Behavior in Animal Model Using SKNY-1, an Oral Drug Candidate for Obesity and Nicotine Addiction Under Definitive Agreement for Acquisition
SKNY-1 was previously shown to achieve up to 30% weight loss, reverse nicotine craving, and preserve muscle mass in an animal model-and is designed to avoid the CNS side effects that halted earlier CB1-targeting drugs MIRA Pharmaceuticals, Inc. (NASDAQ:MIRA) today announced new preclinical results from SKNY-1, an oral drug candidate for obesity and nicotine addiction currently under definitive agreement for acquisition. In a validated behavioral model used to measure Cannabinoid 1 receptor (CB1) related anxiety-like effects, SKNY-1 demonstrated clear reversal of anxiety-related behavior induced by a CB1 activator, setting it apart from earlier CB1-targeting drugs that were discontinued due to serious central nervous system (CNS) effects. SKNY-1 is being developed as a potential oral treatment for obesity and addiction. It has previously been shown to achieve up to 30% weight loss, reverse high-calorie food and nicotine cravings, and preserve muscle mass in preclinical models. These new findings suggest that SKNY-1 may deliver these therapeutic effects without emotional or behavioral disruption, an important factor in long-term treatment adherence. 'These findings are a significant step forward,' said Erez Aminov, Chief Executive Officer of MIRA. 'The ability to suppress appetite and cravings while reversing anxiety-like effects is critical. These results reinforce the differentiated approach behind SKNY-1 and its potential role as a novel oral treatment in large, underserved markets.' About the Study The study used the light-dark preference test in zebrafish-a validated behavioral model to assess anxiety-related responses. Zebrafish naturally prefer darker environments due to an innate fear of predators. However, when anxiety levels are elevated, they avoid the light even more strongly spending more time in the dark. Reduced dark preference (i.e., more time in the light) is interpreted as a calming effect. Four groups were evaluated: Control Group (No Drug): Fish showed balanced behavior between light and dark environments. CP55,940 Group (CB1 Agonist): These animals spent significantly more time in the dark, confirming that CB1 activation increases anxiety at higher doses. Interestingly, at lower doses, CP55,940 produced a calming effect-reducing dark preference and encouraging exploration of the light area. Rimonabant Group (CB1 Inverse Agonist): Fish treated with Rimonabant also showed increased dark-zone time and exhibited a greater increase in anxiety-like behavior than the CB1 agonist group, under both high and low doses of agonist-consistent with the known psychiatric effects that led to Rimonabant's market withdrawal. SKNY-1 Groups: In animals co-treated with CP55,940, SKNY-1 significantly reversed the anxiety-inducing effects of high-dose CP55,940 and enhanced the calming effects at low doses. In all conditions, SKNY-1 brought anxiety-like behavior back to control or better-than-control levels. These results suggest SKNY-1 may help stabilize mood and stress-related behavior-a potential advantage in treating both metabolic and addictive disorders. A New Approach to Endocannabinoid Modulation SKNY-1 targets the endocannabinoid system (ECS)-a key regulator of hunger, emotion, reward, and addictive behavior-through a multi-pathway approach: Biased CB1 antagonism blocks β-arrestin signaling (linked to cravings and compulsive behavior) while preserving G-protein signaling (important for emotional regulation). CB2 partial agonism may reduce inflammation in the brain, which is increasingly recognized as a driver of anxiety, depression, and cognitive decline. By lowering neuroinflammation, SKNY-1 may help preserve emotional balance and support cognitive resilience. Mild inhibition of MAO-B regulates dopamine, which plays a role in motivation and behavioral control. No inhibition of MAO-A confirmed through in vitro screening-important because MAO-A inhibitors are associated with mood instability, drug interactions, and safety concerns. This multi-target profile gives SKNY-1 a differentiated mechanism that may allow it to reduce cravings and weight while supporting emotional health-without the psychiatric side effects that limited earlier CB1 or MAO-based drugs. 'The ability to block cravings while preserving emotional balance is a key challenge in this field,' said Dr. Itzchak Angel, MIRA's Chief Scientific Advisor. 'SKNY-1 appears to meet that challenge head-on. The demonstration that its profile is significantly different than rimonabant in its interaction with CB1 agonists, reinforces the unique pharmacological profile of the drug.' Market Opportunity Obesity and addiction are among the most urgent and expensive public health challenges globally. In the U.S. alone, the economic burden of obesity and related chronic diseases is estimated at $1.7 trillion annually, equivalent to over 9% of the nation's GDP (Milken Institute, 2023). Yet despite significant commercial investment, current therapies remain limited by efficacy gaps and tolerability challenges. Current GLP‑1 therapies like semaglutide deliver weight loss but are injectables, often cause gastrointestinal side effects, and can result in loss of lean muscle mass. Smoking cessation therapies such as varenicline or bupropion offer modest long-term success and may carry psychiatric warnings that restrict their use in sensitive patient populations. Earlier CB1-targeting drugs, including rimonabant, were withdrawn due to severe mood disorders. Furthermore, broad MAO inhibition-especially MAO‑A-has long been associated with mood instability and dangerous food-drug interactions. SKNY‑1 was developed to address those limitations directly. With oral administration, differentiated pharmacology, and potential dual efficacy in obesity and nicotine addiction, SKNY‑1 may offer a best-in-class profile. Its lack of MAO‑A inhibition, confirmed in vitro, further enhances its therapeutic promise. Next Steps MIRA is currently preparing for shareholder approval related to the proposed acquisition of SKNY Pharmaceuticals, Inc. Pending approval, the Company expects to initiate Investigational New Drug (IND)-enabling studies for SKNY-1 as a next step toward human clinical trials. About MIRA Pharmaceuticals, Inc. MIRA Pharmaceuticals, Inc. (NASDAQ:MIRA) is a clinical-stage pharmaceutical company focused on the development and commercialization of novel therapeutics for neurologic, neuropsychiatric, and metabolic disorders. The Company's pipeline includes oral drug candidates designed to address significant unmet medical needs in areas such as neuropathic pain, inflammatory pain, obesity, addiction, anxiety, and cognitive decline. Cautionary Note Regarding Forward-Looking Statements This press release and the statements of MIRA's management related thereto contain 'forward-looking statements,' which are statements other than historical facts made pursuant to the safe harbor provisions of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. These statements may be identified by words such as 'aims,' 'anticipates,' 'believes,' 'could,' 'estimates,' 'expects,' 'forecasts,' 'goal,' 'intends,' 'may,' 'plans,' 'possible,' 'potential,' 'seeks,' 'will,' and variations of these words or similar expressions that are intended to identify forward-looking statements. Any statements in this press release that are not historical facts may be deemed forward-looking. Any forward-looking statements in this press release are based on MIRA's current expectations, estimates, and projections only as of the date of this release and are subject to a number of risks and uncertainties (many of which are beyond MIRA's control) that could cause actual results to differ materially and adversely from those set forth in or implied by such forward-looking statements, including related to MIRA's potential merger with SKNY Pharmaceuticals, Inc. These and other risks concerning MIRA's programs and operations are described in additional detail in the Annual Report on Form 10-K for the year ended December 31, 2024, and the Form 14A filed by MIRA on June 18, 2025, and other SEC filings, which are on file with the SEC at and on MIRA's website at MIRA explicitly disclaims any obligation to update any forward-looking statements except to the extent required by law. Contact: Helga Moya info@ (786) 432-9792 SOURCE: MIRA Pharmaceuticals View the original press release on ACCESS Newswire