Commercial execution
Competing
where it counts

Raveena Gujja lives with obesity in India.
The world is facing a cardiometabolic health crisis. Serious chronic diseases like obesity and diabetes are reshaping societies, straining health systems and intensifying calls for accessible, high-quality products and care.
We are not standing still. Our commercial strategy is built for real‑world impact: expanding access, protecting patient safety and competing where it counts. Guided by our purpose of driving change to defeat serious chronic diseases, we bring scale, speed and responsibility to the challenge, reaching 45.6 million people living with obesity and diabetes in 2025.
Central to this approach is defending and expanding our leadership in the increasingly competitive market for GLP-1 therapies, where we hold close to 43% market share of global volumes. Powered by semaglutide, these game-changing medicines address two of the world’s most pressing health challenges: obesity, impacting over 1 billion people worldwide, and diabetes, affecting around 600 million. Semaglutide is the only molecule that demonstrates cardiovascular protection in both diseases. Our portfolio spans injectable and oral options with FDA‑approved indications to reduce risk of heart attack, stroke or cardiovascular (CV) death – giving us unmatched therapeutic breadth.
We are acting urgently to strengthen our portfolio through targeted investment in next‑generation therapies and business development. Our pipeline across obesity, type 2 diabetes and related comorbidities continues to advance, whilst we enhance optionality by tailoring solutions to individual needs. Building this market taught us that what works for diabetes does not necessarily work for obesity – people with obesity have different concerns, different needs and often prefer more discreet ways to access treatment. Executing this strategy demands market-specific approaches deployed at speed.
“We are acting urgently to strengthen our portfolio through targeted investment in next‑generation therapies and business development”
The US remains our biggest market and demands our boldest moves. We are transforming our position through multiple direct-to-consumer pathways by rapidly expanding our NovoCare® direct-to-patient platform to simplify access and reduce costs, forging new telehealth collaborations and securing retail pharmacy agreements including CVS to improve continuity of care. From 2026, our new agreement with the US Administration – once finalised – will lower prices across Medicare Part D and Medicaid programmes whilst piloting broader obesity coverage – significantly expanding Wegovy® access. We are also pursuing legal action against unlawful sales and marketing of mass compounded drugs, working with regulators, law enforcement and healthcare professionals to protect patients, the US drug approval framework and market integrity.
Outside the US, we are turning challenges into opportunities. As semaglutide nears loss of exclusivity in certain key markets, we are acting decisively, launching second brands in lower‑priced segments, fast‑tracking differentiated devices and sharpening our channel strategies, while reinforcing quality and pharmacovigilance as generics enter the market.
We are playing to win. Backed by robust evidence and patient‑centred execution, we are not just competing in an increasingly challenging landscape – we are reshaping it. Every decision, every initiative and every innovation is driven by our unwavering commitment to get our life-changing medicines to the people who need them – faster than ever before.
OBESITY& RELATED COMORBIDITIES
Expanding the global reach and impact of Wegovy®
Obesity is one of the defining health challenges of our time, impacting almost 1 billion people worldwide. Our goal is to translate scientific leadership into choice, access and evidence – bringing new options to patients and meeting needs across related comorbidities. In 2025, our obesity portfolio delivered 31% sales growth at constant exchange rates (CER), reaching 3.6 million people worldwide.
We have recently expanded the Wegovy® brand with two new offerings: higher‑dose Wegovy® (semaglutide 7.2 mg), which demonstrated 20.7% weight loss in phase 3 studies, and the Wegovy® pill, offering 16.6% weight loss and the convenience of once-daily oral dosing. The latter is the world’s first and only oral GLP‑1‑based medicine to be approved for chronic weight management and is now being produced domestically in the US, with API manufactured at our Clayton, North Carolina site and tablets made and packed at our Durham, North Carolina site.
Momentum continued across launches and label expansions. By the end of 2025, Wegovy® had almost doubled its global footprint to reach 52 countries – with further roll‑outs planned in 2026, subject to local regulatory approvals. In the US, the label was expanded to include treatment of adults with metabolic dysfunction-associated steatohepatitis (MASH) with moderate to advanced liver fibrosis – an important milestone given the high overlap between obesity and metabolic liver disease.
“By the end of 2025, Wegovy® had almost doubled its global footprint to reach 52 countries”
New clinical and real‑world evidence further strengthened the profile of Wegovy® in obesity care. Real‑world data from STEER show a 57% lower risk of heart attack, stroke or death associated with Wegovy® compared with tirzepatide. STEER was conducted among adults with overweight or obesity and established cardiovascular disease, without type 2 diabetes, during periods of continuous treatment (no treatment gaps longer than 30 days). While observational by design and subject to the usual limitations of real‑world data, these findings add to growing evidence that Wegovy® delivers proven cardiovascular protection in addition to meaningful weight loss benefits for appropriate patients.
Beyond clinical endpoints, we are also advancing understanding of how obesity treatments affect everyday life. INFORM, a survey‑based real‑world evidence study, suggested that people taking Wegovy® experienced reduced food noise – persistent, intrusive and unwanted thoughts about food – and improved mental wellbeing. These insights are important for sustained behaviour change and long‑term outcomes, reinforcing the role of GLP‑1 therapy alongside lifestyle support.
Obesity patients reached vs unmet need (2025)
Obesity sales
(DKK billion)OBESITY& RELATED COMORBIDITIES
Breaking down obesity care barriers in the US
Obesity care in the US is at an inflection point. Demand for GLP‑1 medicines is surging, while access remains limited by uneven insurance coverage, affordability barriers and administrative hurdles. In parallel, the spread of unapproved compounded products poses quality and safety risks and can disrupt continuity of care. We are acting across the system – providing near‑term relief for self‑pay patients, partnering to broaden coverage and safeguarding patient safety – so more people can access authorised, FDA‑approved medicines through trusted pathways.
To provide immediate relief for self-paying patients, in November 2025, we introduced an introductory self‑pay offer of USD 199 per month for the first two doses (0.25 mg and 0.5 mg) of Wegovy® or Ozempic® for new self‑pay patients through 31 March 2026, and lowered the standard monthly self‑pay price to USD 349 thereafter. These offers are available across more than 70,000 pharmacies nationwide, with home delivery through NovoCare® Pharmacy and telehealth partners, and are designed to help patients afford authentic, FDA‑approved semaglutide medicines and reduce the lure of unapproved, compounded alternatives.
“We introduced an introductory self‑pay offer of USD 199 per month for the first two doses (0.25 mg and 0.5 mg) of Wegovy® or Ozempic®”
Patient safety underpins everything we do. With the expiry of all FDA grace periods for shortage‑based semaglutide compounding in May 2025, it is now illegal under US compounding laws to make or sell compounded semaglutide drugs, with rare exceptions. Since then, we have stepped up action – pursuing legal remedies against unlawful marketing and sales, and working with regulators, law enforcement, healthcare professionals, patient and provider groups and other stakeholders to protect patients and uphold the integrity of the FDA drug approval framework. We are raising awareness among healthcare professionals and consumers about the safety and efficacy risks of unapproved compounded products, while expanding access to FDA‑approved medicines through trusted pathways, including NovoCare® Pharmacy and telehealth partners.
In addition, we have agreed to a framework with the US Administration to lower semaglutide prices across Medicare Part D (government insurance for seniors), Medicaid (government insurance for low-income Americans) and direct‑to‑patient channels from 2026 onwards, and to broaden coverage through a Medicare pilot programme for Part D beneficiaries with qualifying comorbidities. This agreement is a significant step toward expanding access to authentic, FDA-approved obesity and diabetes medicines for millions of people living in the US. We are finalising details and remain committed to constructive dialogue.
DIABETES& RELATED COMORBIDITIES
Additional Ozempic® benefits drive strengthened diabetes leadership
The global burden of diabetes and related complications is vast. By developing products that meet the complex needs of people living with diabetes, our innovations create long-term value for health systems and society. In 2025, we reached 42 million people with our diabetes portfolio, delivering 4% sales growth at CER.
Against this backdrop, the clinical profile of semaglutide – our flagship GLP-1 innovation – continued to strengthen. Regulatory authorities in Europe and the US now recognise its cardiovascular benefits, with the FDA approving Rybelsus® (oral semaglutide) to reduce the risk of major adverse cardiovascular events in adults with type 2 diabetes at high risk. Rybelsus® is the only oral GLP‑1 therapy shown to lower blood glucose and body weight with a confirmed cardiovascular benefit, highlighting the comprehensive benefits of semaglutide.
Meanwhile, Ozempic® – the injectable form of semaglutide approved for the treatment of type 2 diabetes – is proving its worth in new areas. The phase 3b STRIDE study showed that Ozempic® helped people with peripheral arterial disease walk further without pain, leading European regulators to update the medicine’s label to reflect these mobility and quality-of-life improvements. In the US, the FDA approved Ozempic® – based on results from the FLOW trial – to reduce the risk of kidney disease progression, kidney failure and cardiovascular death in adults with type 2 diabetes and chronic kidney disease (CKD), making Ozempic® the only medicine in its class with a CKD indication.
Diabetes patients reached vs unmet need (2025)
Diabetes sales
(DKK billion)DIABETES& RELATED COMORBIDITIES
Simplifying insulin treatment with once-weekly options
For many adults with diabetes, basal insulin is essential yet burdensome: daily injections, complex titration and busy schedules can hinder adherence. Awiqli® – the world’s first and only once‑weekly basal insulin – reduces the treatment burden, helping both people with diabetes and healthcare professionals stay focused on achieving and maintaining individual glycaemic targets. As a once‑weekly option, it reduces the weekly injection burden from seven to one.
Awiqli® is approved in the EU and 12 other countries, with launches progressing across markets. In the US, we resubmitted the Biologics License Application to the FDA in September 2025, following a 2024 action letter. Further reviews are underway in other markets and additional approvals are expected in 2026.
This rollout is underpinned by evidence from ONWARDS – five phase 3a trials in about 4,000 adults with type 2 diabetes – where change in HbA1c was the primary endpoint, supporting clinical decision‑making.
Alongside Awiqli®, our once‑weekly portfolio advanced with the European Commission’s approval of Kyinsu® (IcoSema), a once‑weekly combination of basal insulin icodec and the GLP‑1 RA semaglutide. The decision, based on the COMBINE phase 3a programme where all three trials met primary endpoints, confirms a well‑tolerated safety profile and expands options for adults insufficiently controlled on basal insulin or GLP‑1 RAs.
Nathalia de Souza Santos lives with type 1 diabetes in Brazil.
RARE DISEASE
Expanding therapeutic impact in rare bleeding and growth disorders
Novo Nordisk has a rich legacy and an enduring commitment to people living with rare diseases. Our portfolio is focused on innovative medicines that combine strong efficacy profiles with simple administration to ease the treatment burden.
In 2025, our rare disease portfolio delivered 9% sales growth at CER, with Sogroya® leading in the long‑acting growth hormone segment across launch markets and Alhemo® expanding its presence in haemophilia prophylaxis.
Sogroya®, our long-acting growth hormone treatment, gained significant momentum in 2025 as new international consensus guidance standardised the approach to paediatric growth hormone deficiency. This clinical framework – covering diagnosis, dosing and weekly monitoring regimens – is helping clinicians deliver more consistent care and expanding access to treatment. Building on this foundation, we maintained Sogroya®’s leadership across its first five launch markets whilst expanding into France, Argentina and Canada, with further entries planned for 2026.
In rare bleeding disorders, the FDA and EMA approved expanded use of Alhemo® for people aged 12 or older with haemophilia A or B without inhibitors, broadening access and sustaining our momentum in this therapy area while addressing the remaining unmet needs in haemophilia B.
Rare disease sales
(DKK billion)“Our portfolio is focused on innovative medicines that combine strong efficacy profiles with simple administration to ease the treatment burden”
PRODUCTION
Strategic investments to expand manufacturing capacity
In February 2025, the FDA declared the shortage of semaglutide injectables resolved, confirming that supply meets or exceeds current and projected US demand. To ensure consistent, sustainable access to authentic, FDA‑approved medicines, we are continuing to expand US manufacturing capacity and to strengthen our supply chain.
Patient safety and uninterrupted care remain our top priorities. Following the FDA’s declaration, we continue to work closely with regulators and supply partners to ensure consistent availability and reduce the risk of interruptions as demand continues to evolve.
We strive to operate our US production facilities around the clock and have accelerated capital expenditure, including approximately USD 2 billion in US manufacturing in 2025 and plans to invest a further USD 5.6 billion towards 2028. These investments will add new lines, increase fill‑finish and packaging capacity, and significantly expand multiple US sites to address national supply needs.
This complements ongoing work to scale production across our global manufacturing network, with major expansions underway in Denmark, France, Brazil and China. Following our 2024 acquisition of three fill‑finish sites formerly operated by Catalent Inc., these facilities are now being transitioned into our network. Once fully integrated, they will enhance flexibility and optionality across the supply chain and complement our significant internal expansions.
Expansion at our Clayton, North Carolina site in the US.
“Patient safety and uninterrupted care remain our top priorities”
Product overview1
obesity
GLP-1
- Saxenda®, liraglutide 3.0 mg
- Wegovy®, semaglutide 2.4 mg
- Wegovy® pill, semaglutide 25 mg
Obesity delivery systems
- Saxenda®, FlexTouch®
- Wegovy®, Single Dose Device and FlexTouch®
diabetes
Once-weekly insulin
- Awiqli®, insulin icodec
New generation insulin and combinations
- Tresiba®, insulin degludec
- Ryzodeg®, insulin degludec/insulin aspart
- Fiasp®, fast-acting insulin aspart
- Xultophy®2, insulin degludec/liraglutide
Modern insulin
- Levemir®, insulin detemir
- NovoRapid®3, insulin aspart
- NovoMix® 30, biphasic insulin aspart
- NovoMix® 50, biphasic insulin aspart
Human insulin
- Insulatard® isophane (NPH) insulin
- Actrapid®, regular human insulin
- Mixtard® 30, biphasic human insulin
- Mixtard® 50, biphasic human insulin
GLP-1
- Victoza®, liraglutide
- Ozempic®, semaglutide
- Rybelsus®, oral semaglutide
Pre-filled delivery systems
- FlexTouch®, U100, U200, U700
- FlexPen®
- InnoLet®
- Ozempic®, FlexTouch®
Durable delivery systems
- NovoPen® 6
- NovoPen® 5
- NovoPen® 4
- NovoPen Echo® Plus
- NovoPen Echo®
Other delivery systems
- PumpCart®, NovoRapid® and Fiasp® cartridge to be used in pump
- Penfill® cartridge
Oral antidiabetic agents
- NovoNorm®, repaglinide
Glucagon
- GlucaGen®, glucagon (vial and Hypokit®)
- Zegalogue®, dasiglucagon
Needles
- NovoFine® Plus
- NovoFine®
- NovoTwist®
- NovoFine® AutoCover®
rare disease
Rare blood disorders
- NovoSeven®4, eptacog alfa
- NovoEight®5, turoctocog alfa
- Esperoct®, turoctocog alfa pegol, N8-GP
- Alhemo®, concizumab
- Refixia®6, nonacog beta pegol, N9-GP
- NovoThirteen®7, catridecacog
Rare haemato-renal disorders
- Rivfloza™, nedosiran
Rare endocrine disorders
- Norditropin®, somatropin
- Sogroya®, somapacitan
Pre-filled human growth hormone delivery systems
- FlexPro®
Other delivery systems
- PenMate®, automatic needle inserter for FlexPro®
Hormone replacement therapies
- Vagifem®8, estradiol hemihydrate
- Activelle®, estradiol/norethisterone acetate
- Eviana®, estradiol/norethisterone acetate
- Kliogest®, estradiol/norethisterone acetate
- Novofem®, estradiol/norethisterone acetate
- Trisequens®, estradiol/norethisterone acetate
- Estrofem®, estradiol
1. Products listed may not be available or approved in all markets.
2. In the US approved under the brand name Xultophy® 100/3.6.
3. In the US approved as NovoLog®.
4. In the US approved as NovoSeven® RT.
5. In the US approved as Novoeight®.
6. In the US approved under the name of REBINYN®.
7. In the US approved under the name tretten®.
8. In the UK also approved as gina®.
Patent status for products with marketing authorisation
The patent expiry dates for products with marketing authorisation1 are shown in the tables below. The dates provided are for expiry in the US, China, Japan and Europe of patents on the active ingredient, unless otherwise indicated, and include actual and estimated extensions of patent term, when applicable. For several products, in addition to the active ingredient patent, Novo Nordisk holds other patents on manufacturing processes, formulations or uses that may be relevant for exclusivity beyond the expiration of the active ingredient patent. Furthermore, regulatory data protection and/or orphan exclusivity may apply.
obesity
Product |
|
US |
|
China |
|
Japan |
|
Europe2 |
|---|---|---|---|---|---|---|---|---|
Wegovy® injection |
|
2032 |
|
2026 |
|
2031 |
|
2031 |
Wegovy® pill |
|
2032 |
|
2026 |
|
2031 |
|
2031 |
Saxenda® |
|
Expired |
|
Expired |
|
Expired |
|
Expired |
diabetes
Product |
|
US |
|
China |
|
Japan |
|
Europe2 |
|---|---|---|---|---|---|---|---|---|
Ozempic® |
|
2032 |
|
2026 |
|
2031 |
|
2031 |
Rybelsus® |
|
2032 |
|
2026 |
|
2031 |
|
2031 |
Tresiba® |
|
2029 |
|
Expired |
|
2027 |
|
2028 |
Xultophy® |
|
2029 |
|
Expired |
|
Expired |
|
2028 |
Ryzodeg® |
|
2029 |
|
Expired |
|
Expired |
|
2028 |
Victoza® |
|
Expired |
|
Expired |
|
Expired |
|
Expired |
Human insulin and Modern insulins3 |
|
Expired |
|
Expired |
|
Expired |
|
Expired |
rare disease
Product |
|
US |
|
China |
|
Japan |
|
Europe2 |
|||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
NovoSeven® |
|
Expired |
|
Expired |
|
Expired |
|
Expired |
|||||||
Norditropin® |
|
Expired |
|
Expired |
|
Expired |
|
Expired |
|||||||
|
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