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Photo: Bloomberg.com
Novo Nordisk is facing one of the most challenging periods in its modern history. After years of being celebrated as the pioneer behind the global weight loss drug revolution, the Danish pharmaceutical giant is now under intense scrutiny from investors questioning whether scientific leadership can still translate into durable financial returns.
The pressure has been severe. Novo’s share price has fallen roughly 50 percent year to date, marking its worst performance since listing in Copenhagen more than 30 years ago. At its peak in mid-2024, the stock traded above 1,000 Danish kroner. It now hovers near 320 kroner, a collapse that triggered the largest leadership shakeup in the company’s 100-year history.
While investors grow impatient, scientists argue that the real value of Novo’s GLP-1 drugs is still unfolding.
Semaglutide, sold under the brand names Ozempic and Wegovy, reshaped modern obesity treatment. Originally developed to control blood sugar in diabetes patients, the drug’s appetite suppressing effects quickly led to widespread off-label use. It is now fully approved for obesity and generates tens of billions of dollars annually for Novo Nordisk.
Beyond weight loss, semaglutide has gained regulatory approvals for reducing cardiovascular risk in overweight patients, treating chronic kidney disease in diabetics, and most recently, liver disease. These expanding indications underline the drug’s versatility and long-term medical relevance.
However, the commercial landscape has changed rapidly. U.S. rival Eli Lilly has surged ahead with tirzepatide, marketed as Mounjaro and Zepbound, which targets both GLP-1 and GIP hormones. Tirzepatide has already secured approval for treating moderate to severe obstructive sleep apnea in adults with obesity, adding to investor perceptions that Lilly’s pipeline is moving faster and broader.
One of the most intriguing developments around GLP-1 drugs is their potential impact on the brain. Observational data increasingly suggests that these medicines dampen reward-driven cravings beyond food, including alcohol, nicotine, and even compulsive behaviors.
Researchers believe GLP-1 drugs influence dopamine signaling in the brain’s reward pathways, helping patients regain control over impulsive consumption. Small clinical trials have already shown that low-dose semaglutide significantly reduced alcohol intake and cravings in patients with alcohol use disorder within weeks of treatment.
Scientists now describe GLP-1 drugs as potential “anti-consumption” therapies, with possible applications spanning addiction, obesity, and behavioral disorders. These findings have opened new research avenues that extend far beyond weight management, reinforcing the long-term scientific relevance of Novo’s platform.
Investor sentiment took another hit in November when Novo released results from a two-year clinical trial testing semaglutide in patients with Alzheimer’s disease. The trial failed to meet its primary endpoint, showing no statistically significant slowing of cognitive decline. Novo subsequently discontinued a one-year trial extension.
The market reaction was swift. Shares dropped nearly 6 percent in a single session, despite management having previously described the study as a high-risk, exploratory effort.
Scientists, however, urged caution in labeling the trial a failure. Biomarker data showed that semaglutide reduced Alzheimer’s-related proteins in cerebrospinal fluid and lowered systemic inflammation, both considered meaningful biological signals. Experts suggest the drug’s real potential may lie in prevention rather than treatment, particularly if administered earlier in the disease process.
This mirrors the broader Alzheimer’s drug journey, where decades of failed trials eventually led to therapies that can now slow disease progression by roughly one third, albeit with safety tradeoffs.
Despite Novo’s scientific progress, investor concerns are rooted in timing and competition. Drug development is inherently slow, while public markets demand near-term clarity on earnings growth. Adding new indications requires years of trials, regulatory reviews, and reimbursement negotiations.
Patent risk adds further pressure. Semaglutide faces key patent expirations in 2031 and 2032, opening the door to generics and cheaper compounded alternatives. Analysts argue that Novo is entering a critical five-year window without a sufficiently strong commercial moat to protect pricing power.
Political pressure compounds the problem. Calls to lower drug prices in the United States, along with potential import tariffs, threaten margins across the pharmaceutical sector and weigh particularly heavily on blockbuster drugs.
Wall Street remains split on Novo’s future. More cautious analysts argue that falling prices, generic competition, and aggressive rivals could continue to compress valuation. Some have questioned whether a clear valuation floor exists before patent protection weakens further.
Others are more constructive. Bullish analysts believe expectations have reset too far and that volume growth in the global obesity market could still support long-term revenue. They point to pipeline assets such as CagriSema and oral formulations of Wegovy as potential upside drivers if prescription trends rebound.
Still, even optimists concede that evidence of sustained script growth will be required before investors regain confidence.
At its core, Novo Nordisk’s challenge is not scientific credibility but timing. The medical community sees GLP-1 drugs as transformative tools with decades of potential ahead. Investors, by contrast, are focused on competition, margins, and the finite life of patents.
The disconnect leaves Novo caught between two realities. The science continues to advance, quietly expanding into new therapeutic frontiers, while the stock market demands faster proof of financial payoff. Whether Novo can bridge that gap may determine not only its valuation, but its place in the next chapter of pharmaceutical innovation.









