Eli Lilly now commands a 60% share of the global prescription obesity drug market, a dominance that explains why its stock has surged 58% over the past year while Novo Nordisk shares have fallen 5%. The two companies together control about 87% of obesity drug revenue, but Lilly's lead is driven by the popularity and efficacy of its Zepbound GLP-1 treatment. The global obesity drug market reached $66 billion in 2025 and is projected by Bloomberg to hit $120 billion by 2030. Novo Nordisk recently launched its obesity drug Wegovy in pill form and raised its sales and profit forecasts, signaling that the competitive race is far from over.
Novo Nordisk Expands Semaglutide Beyond Cardiometabolic Care as Lilly Rivalry Intensifies
Novo Nordisk is pushing to extract greater value from semaglutide by expanding its use beyond traditional diabetes, obesity and cardiovascular indications, even as it faces intense competition from Eli Lilly across cardiometabolic care. Semaglutide-based GLP-1 products, including Ozempic and Rybelsus for type II diabetes and Wegovy for obesity, accounted for roughly 75.5% of Novo's adjusted first-half 2026 sales, leaving the company highly exposed to changes in competition, pricing and market share. The clearest example of the expansion came with Wegovy's 2025 U.S. approval for noncirrhotic metabolic dysfunction-associated steatohepatitis in adults with moderate-to-advanced liver fibrosis, and in March 2026 the European Commission granted conditional authorization to Kayshild, or semaglutide, for adults with noncirrhotic MASH and F2-F3 liver fibrosis. Novo is also building evidence in knee osteoarthritis, where the STEP 9 study showed significant improvements in pain and physical function among adults with obesity, and in post-hoc analyses of obstructive sleep apnea and asthma-related outcomes, though these remain opportunities rather than established indications. The company's Alzheimer's disease program for semaglutide was discontinued after the phase III EVOKE and EVOKE+ studies failed to meet their primary endpoints. Eli Lilly is pursuing a similarly broad strategy, with Mounjaro approved in the United States to reduce major cardiovascular events in adults with T2D at high cardiovascular risk, Zepbound approved for adults with obesity and moderate-to-severe OSA, the oral GLP-1 pill Foundayo being studied across multiple conditions, and retatrutide in late-stage studies. In MASH, Madrigal Pharmaceuticals' Rezdiffra generated $675.6 million in first-half 2026 sales, up 93% year over year, while Altimmune's pemvidutide is in the phase III PERFORMA study with a potential 52-week readout not expected until 2029. Year to date, Novo shares have lost 26.2% against the industry's 8.9% growth, and the stock trades at 10.92 forward earnings versus 17.49 for the industry, while 2026 earnings estimates have risen from $3.40 to $3.53 per share over the past 60 days.
Biotech & Genomic Medicine › Metabolic, Diabetes & Obesity Competition
Aging Population › Chronic-Disease Pharma Franchises Competition
Longevity & Life Extension › GLP-1 Healthspan Proxies Competition
NVO · Technology · Positive Wegovy's U.S. MASH approval and EU conditional authorization of Kayshild expand semaglutide beyond cardiometabolic indications
LLY · Competition · Negative Novo Nordisk is expanding semaglutide into new indications, intensifying rivalry with Lilly across cardiometabolic care
MDGL · Competition · Neutral Madrigal's Rezdiffra MASH sales cited as context in the GLP-1 MASH competition landscape
AstraZeneca Opens US$1b R&D Center in Kendall Square
AstraZeneca has opened a new US$1b global research and development center in Kendall Square, Massachusetts, consolidating its US work in oncology, cell therapy, chronic and rare diseases, and obesity into a single expanded hub. The site uses robotics and AI-enabled automation to support the company's research programs and broader drug development efforts. AstraZeneca is a GB-based biopharmaceutical group with a £185.5 billion market cap that spends heavily on discovering and developing prescription medicines. The company said the center tightens the link between early science and late-stage assets, which could affect how quickly it refines drug candidates and retires weaker programs. Investors will be watching for Phase II or Phase III readouts in obesity, COPD and key oncology programs over 2027 to 2029 as markers of whether the build-out is translating into a more resilient portfolio mix.
Biotech & Genomic Medicine › Oncology Therapeutics Capital
Biotech & Genomic Medicine › Metabolic, Diabetes & Obesity Capital
Biotech & Genomic Medicine › Immuno-Oncology / Checkpoint Capital
Biotech & Genomic Medicine › Cell Therapy (CAR-T & beyond) Capital
AZN.LSE · Technology · Positive AstraZeneca opened a $1B R&D center using robotics and AI to speed drug discovery and refine candidates across oncology, cell therapy, and obesity.
Novo Nordisk Rated Zacks Rank #3 as Earnings Estimates Rise
Novo Nordisk is rated Zacks Rank #3 (Hold), with the Zacks Consensus Estimate for the current quarter rising 6.9% over the last 30 days to $0.80 per share, a year-over-year change of -21.6%. For the current fiscal year, the consensus earnings estimate of $3.53 points to a change of -10.9% from the prior year and has moved +2.4% over the last 30 days, while the next fiscal year's estimate of $3.41 indicates a -3.5% change and has slipped -0.3% over the past month. Consensus sales estimates stand at $11.41 billion for the current quarter, $46.1 billion for the current fiscal year and $47.16 billion for the next fiscal year, indicating changes of -2.8%, -1.5% and +2.3%, respectively. In the last reported quarter, Novo Nordisk posted revenues of $12.21 billion, up 4.5% year over year and an 8.34% surprise over the Zacks Consensus Estimate of $11.27 billion, with EPS of $0.96 versus $0.97 a year ago and a +17.07% EPS surprise. The stock is graded A on the Zacks Value Style Score, indicating it trades at a discount to its peers, though its Zacks Rank #3 suggests it may perform in line with the broader market near term.
Aging Population › Chronic-Disease Pharma Franchises Capital
Biotech & Genomic Medicine › Metabolic, Diabetes & Obesity Capital
Longevity & Life Extension › GLP-1 Healthspan Proxies Capital
NVO · Capital · Neutral Zacks Rank #3 (Hold) with consensus earnings estimates rising 6.9% for the current quarter but still down year over year, an analyst-valuation update.
Sanofi, Novartis and Novo Nordisk Lead Week of Multi-Billion-Dollar Healthcare Deals
A Delaware federal judge on Monday rejected requests from Pfizer, BioNTech and Moderna to dismiss lawsuits filed by Bayer's Monsanto unit over their use of US Patent No. 7,741,118, a patent related to mRNA technology, with Judge William Bryson saying the companies failed to prove the patent was invalid or not infringed by their COVID-19 vaccines. Sanofi agreed to a deal worth up to $8B, including $1B upfront, with Regeneron to jointly develop four long-acting immunology therapies, led by the clinical-stage IL-13 monoclonal antibody REGN20423. China's Abogen Biosciences signed a licensing and option agreement with Novartis worth up to $7.8B, comprising a $575 million upfront payment and up to approximately $7.2 billion in potential milestone payments if all options on all programs are exercised, covering an exclusive worldwide license to Abogen's lead asset ABO2203. Jiangsu Hengrui Pharmaceuticals agreed to license global rights to its experimental obesity drug HRS-1596 to Novo Nordisk in a deal worth up to $2.6B, with $300M upfront and the transaction expected to close in Q4 2026. Meanwhile, the S&P 500 Health Care Sector Index slipped 2.66% for the week, with Incyte down 6.93% and Regeneron down 6.71% among the top decliners, while McKesson rose 4.11% and Cardinal Health gained 3.67%.
Dexcom Report Flags CGM Growth Opportunity in Type 2 Diabetes Care
Dexcom released its 2026 "State of Type 2 Report: Global Access and Attitudes to Diabetes Technology" ahead of the 62nd Annual Meeting of the European Association for the Study of Diabetes, highlighting gaps in continuous glucose monitoring awareness and access while pointing to growing potential for combining CGM with GLP-1 therapies. The survey of more than 800 healthcare professionals and 2,500 people with Type 2 diabetes across eight countries found that 89% of HCPs believe CGM helps assess treatment adherence between appointments, yet 55% of surveyed Type 2 patients reported limited knowledge of the technology, and reimbursement and coverage challenges were cited by 90% of U.S. HCPs and 53% of HCPs in the other seven countries surveyed. Among existing users, 94% said CGM helps them manage diabetes more independently and 91% use CGM data to guide treatment decisions. The report also flagged an emerging intersection between CGM and GLP-1 therapies, with 58% of Type 2 patients taking GLP-1 medicines using CGM alongside their medication versus only 27% of Type 2 patients not using insulin, while half of HCPs expect increasing GLP-1 use to drive CGM adoption. Dexcom also partnered with Team Novo Nordisk, an all-diabetic professional cycling team principally sponsored by Novo Nordisk, to extend its visibility within the Type 1 diabetes community and create opportunities for real-world research, education and awareness.
Biotech & Genomic Medicine › Metabolic, Diabetes & Obesity ▲Demand
Biotech & Genomic Medicine › Diagnostics & Precision Testing ▲Demand
DXCM · Demand · Positive Dexcom's own report flags large untapped CGM awareness/access gaps and growing CGM+GLP-1 adoption potential, supporting its product demand outlook.
NVO · Demand · Positive Report shows 58% of Type 2 patients on GLP-1 medicines use CGM and half of HCPs expect rising GLP-1 use to drive CGM adoption, plus Novo Nordisk's Team Novo Nordisk partnership with Dexcom.
Eli Lilly Reports New Efficacy Data for Foundayo, EloraTZP and Ebglyss at EASD
Eli Lilly and Company presented new efficacy data from studies of its marketed and investigational metabolic medicines at the annual European Association for the Study of Diabetes conference. In the phase III ACHIEVE-4 study, Foundayo (orforglipron), a once-daily oral GLP-1 receptor agonist approved for chronic weight management, demonstrated a non-inferior risk of major adverse cardiovascular events versus titrated insulin glargine, with MACE-4 risk 16% lower, MACE-3 risk 23% lower, cardiovascular death risk 53% lower and all-cause death risk 57% lower; at 52 weeks A1C declined 1.6% versus 1% and body weight fell 8.8% versus a 1.7% increase, while 10.6% discontinued due to adverse events. Lilly also reported positive 48-week results from a phase IIb study of EloraTZP, an investigational combination of eloralintide and Zepbound, in adults with obesity or overweight and type II diabetes, where the highest-dose combination of 9 mg eloralintide plus 15 mg Zepbound reduced body weight by 23.3% (54.1 pounds) versus 14.8% (34.4 pounds) for Zepbound 15 mg alone, and A1C declined 2.9% versus 2.4%. Separately, the phase IIIb ADtouch study of Ebglyss (lebrikizumab-lbkz) met its primary and secondary endpoints, with 53% of patients on monotherapy achieving clear or almost clear hands and feet at week 16 versus 27% with placebo, and Lilly has submitted the data to the FDA seeking a potential U.S. label expansion to include localized atopic dermatitis with moderate-to-severe hand and foot involvement. Lilly has also submitted a regulatory filing to the FDA seeking approval of Foundayo for the treatment of type II diabetes, with the application currently under review, intensifying its oral GLP-1 competition with Novo Nordisk's oral Wegovy, Ozempic and Rybelsus.
Biotech & Genomic Medicine › Metabolic, Diabetes & Obesity ▲Competition
Longevity & Life Extension › GLP-1 Healthspan Proxies ▲Competition
LLY · Technology · Positive Positive efficacy data for Foundayo, EloraTZP and Ebglyss, plus FDA submissions for label expansion and type II diabetes approval.
NVO · Competition · Negative Lilly's Foundayo type II diabetes filing intensifies oral GLP-1 competition with Novo Nordisk's oral Wegovy, Ozempic and Rybelsus.