Novo Nordisk reported Q3 2025 earnings on November 5, showing continued strong demand for its weight-loss drug Wegovy, despite rising costs and pricing pressure forcing the company to narrow its full-year guidance.
The drugmaker reported a 15% increase in U.S. sales at Constant Exchange Rates (CER) in the first nine months of 2025, with operating profit increasing 10% to Danish Kroner (DKK) 95.9 billion ($14.7 billion).
If one-time restructuring charges of approximately DKK 9 billion were excluded, the operating profit would have increased by 21%.
Free cash flow decreased to DKK 63.9 billion from DKK 71.8 billion in 2024, and the company announced DKK 53 billion in shareholder returns, primarily through dividend payments.
Obesity care growth, led by Wegovy, surged 41% to DKK 59.9 billion, while GLP-1 diabetes treatments grew 10%, with sales of rare disease treatments increasing 13%.
Despite the strong results, the company’s stock was down 3.9%, marking a 45% year-to-date decline.
Novo Nordisk stated that the obesity segment accounts for the bulk of its growth, with a global GLP-1 market share of 59%.
Yet, the company trimmed its full-year guidance, suggesting lower growth expectations for GLP-1 amid rising competition and pricing pressure in the U.S. market.
Now, the company has announced FDA’s approval of Wegovy for the treatment of MASH (Metabolic Dysfunction-Associated Steatohepatitis), a form of fatty-liver disease that can lead to liver failure.
The approval opens a new potential market for Wegovy, strengthening Novo Nordisk’s long-term growth prospects.
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In addition, Novo Nordisk agreed to acquire biotech Akero Therapeutics and its Phase 3 drug, an FGF21 analogue, for the treatment of MASH.
Bringing Wegovy and Akero together could give Nordisk a commanding position in the emerging market for metabolic liver diseases.
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Expanding its market in rare diseases, Novo is also buying Omeros’ MASP-3 inhibitor zaltenibart, a clinical-stage drug targeting rare blood disorders.
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Novo has submitted Mim8 for approval in the EU and the U.S. It’s a bispecific antibody used to prevent bleeding in people with hemophilia A, a rare genetic blood disorder.
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The drugmaker has also initiated phase 3 development of Cagrilintide, potentially the first amylin monotherapy for weight management.

