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Novo Nordisk vs. Amgen: Which Pharma Stock Is the Better Buy?
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Key Takeaways
Novo Nordisk leads the GLP-1 market with Ozempic, Rybelsus and Wegovy across diabetes and obesity.
Amgen brings a diversified portfolio across oncology, CV disease, inflammation, bone health and rare diseases.
MariTide is in phase III obesity studies and is being tested for monthly dosing versus weekly injections.
Novo Nordisk (NVO - Free Report) and Amgen (AMGN - Free Report) are both global healthcare heavyweights with the scale, financial strength and research depth needed to turn scientific innovation into blockbuster drugs. Each company has built a reputation for durable franchises, strong pricing power and steady demand across critical treatment areas, making both stocks compelling long-term plays in the pharma sector.
Novo Nordisk is widely recognized as the market leader in the GLP-1 space, marketing its semaglutide drugs under brand names Ozempic (pre-filled pen and oral tablet) and Rybelsus (oral tablet) for type II diabetes (T2D), and Wegovy (injection and pill) for chronic weight management. Amgen, meanwhile, brings a more diversified portfolio across oncology, cardiovascular (CV) disease, inflammation, bone health and rare disease markets. It has some key pipeline assets, with a focus on the lead obesity candidate, MariTide.
That sets up a strong head-to-head debate: should investors favor Novo Nordisk’s concentrated exposure to the fast-growing GLP-1 market, or Amgen’s broader, more balanced biotech model with income-friendly characteristics? For investors weighing growth, resilience and risk, this pharma faceoff offers a timely look at two very different paths to long-term returns.
Let's examine the fundamentals of the two stocks to make a prudent choice.
The Case for NVO Stock
Novo Nordisk has achieved tremendous success in the cardiometabolic treatment space, driven primarily by Ozempic, Rybelsus and Wegovy. As of 2025-end, Novo Nordisk remained the market leader with a total GLP-1 volume market share of 54.6% globally across diabetes and obesity care.
Novo Nordisk is pursuing new indications for its semaglutide drugs, including CV and other indications. In 2025, Rybelsus became the first oral therapy approved in the United States to lower the risk of major adverse CV events in high-risk T2D patients, regardless of prior CV history. Wegovy’s label includes CV, HFpEF and osteoarthritis indications, while Ozempic remains the only GLP-1 approved to slow kidney disease and reduce CV death in patients with diabetes. Higher-dose Wegovy injections have been approved in the United States and the EU, expanding its portfolio and enabling the company to tailor treatment options better to meet the diverse needs and preferences of obesity patients. NVO is also seeking to expand Ozempic’s label to include peripheral artery disease.
In late December, the FDA also approved NVO’s 25 mg oral semaglutide (Wegovy pill) for obesity and CV disease, which was subsequently launched in early January. The FDA recently approved an oral version of Ozempic (1.5 mg, 4 mg and 9 mg) for adult T2D patients, which was subsequently launched in the United States. A supplemental application for a higher 25 mg tablet is also under review, with a regulatory decision expected by the end of 2026. Novo Nordisk also intends to seek regulatory approval for both Rybelsus and oral Ozempic in children and adolescents aged 10 to 17 years with T2D in the United States and the EU in the second half of 2026.
Novo Nordisk is advancing its next-generation obesity pipeline. It has submitted a regulatory filing seeking the approval of CagriSema injection, a follow-up drug to Wegovy, for obesity. Meanwhile, its mid-stage asset, amycretin, has shown strong weight-loss efficacy in a phase II study and is slated to enter phase III soon. The company has bolstered its pipeline through several major collaborations and acquisition deals.
Beyond GLP-1s, NVO is building its Rare Disease franchise, advancing Mim8 in hemophilia A, and securing both EU and U.S. approvals for Alhemo to treat hemophilia A and B, with or without inhibitors. Meanwhile, the FDA has granted accelerated approval for Wegovy in treating MASH with fibrosis. Novo Nordisk and rival Eli Lilly (LLY - Free Report) have also introduced multiple price cuts in response to pressure from the U.S. government during 2025 and 2026 to improve patient access to GLP-1 medicines.
Despite the recent wins, Novo Nordisk is far from being out of the woods yet. It has been facing increasing competition from Eli Lilly, which markets its tirzepatide (GLP-1) medicines as Mounjaro for T2D and Zepbound for obesity. Despite being on the market for just over three years, these drugs have become LLY’s key top-line drivers. Lilly recently secured FDA approval of its oral GLP-1 drug, orforglipron, for adults with obesity or overweight with weight-related medical problems, marketed under the brand name Foundayo. The drug competes directly with NVO’s Wegovy pill.
Although Novo Nordisk’s post-first-quarter guidance raise offered some reassurance, the bigger picture remains cautious — management still expects both sales and operating profit to decline in 2026, underscoring weak core momentum and mounting structural challenges. The modestly improved outlook reflects stronger GLP-1 demand, broader adoption of obesity treatments and ongoing Wegovy launches. However, these positives are being offset by U.S. pricing pressure, softer injectable GLP-1 prescription trends, reduced Medicaid obesity coverage, intensifying competition from Eli Lilly, “Most Favored Nation” pricing agreement, gradual semaglutide exclusivity losses in select markets and elevated spending on R&D, manufacturing and commercial expansion.
The Case for AMGN Stock
Amgen’s diverse portfolio and global reach position it well in a changing pharma landscape. Key medicines like Repatha, Evenity and Blincyto, as well as newer medicines like Tavneos, Tezspire, and Imdelltra, are driving sales, more than offsetting declining revenues from oncology biosimilars and mature products like Enbrel. New biosimilar launches are also contributing to top-line growth.
The 2023 acquisition of Horizon Therapeutics has significantly expanded Amgen's rare disease business by adding several rare disease drugs, including Tepezza, Krystexxa and Uplizna, to its portfolio. Amgen is also pursuing label expansions for its marketed drugs to broaden their approved uses and expand the addressable patient population. Approval for the expanded use of these drugs can potentially drive further top-line growth.
Amgen’s key pipeline candidate is MariTide, a GIPR/GLP-1 receptor, which is being evaluated for T2D, obesity and obesity-related conditions as part of its comprehensive MARITIME phase III program. Amgen has nine global phase III studies underway with MariTide in obesity, and other obesity-related conditions like obstructive sleep apnea, cardiovascular disease and heart failure. Three phase III studies of MariTide in T2D will be initiated in 2026.
Unlike the currently marketed obesity drugs like Eli Lilly’s Zepbound and Novo Nordisk’s Wegovy, which require weekly injections, MariTide is being tested for monthly dosing. A less frequent dosing regimen is expected to reduce treatment burden and thereby boost patient adherence. In prior clinical studies, the candidate has shown predictable and sustained weight loss and a meaningful impact on cardiometabolic parameters.
Beyond obesity, Amgen has promising late-stage pipeline drugs across several therapeutic areas, which represent significant commercial potential. These include olpasiran (for atherosclerotic CV disease), xaluritamig (metastatic castrate-resistant prostate cancer), daxdilimab (primary discoid lupus erythematosus) and dazodalibep (Sjögren’s disease).
Amgen also boasts a strong biosimilars portfolio, which includes Bekemv (biosimilar of AstraZeneca’s Soliris), Wezlana (J&J’s Stelara) and Pavblu (Regeneron’s Eylea). It is also developing biosimilar versions of blockbuster oncology drugs like Bristol Myers’ Opdivo, Merck’s Keytruda and Roche’s Ocrevus in phase III studies.
However, pricing headwinds and competitive pressure are negatively impacting the sales of many products. Sales of best-selling drugs, Prolia and Xgeva, are expected to decline in the upcoming quarters due to generic erosion following the loss of patent protection.
How Do Estimates Compare for NVO & AMGN?
The Zacks Consensus Estimate for Novo Nordisk’s 2026 sales and earnings per share (EPS) implies a year-over-year decline of around 3.6% and 12.6%, respectively. EPS estimates for 2026 have been trending upward over the past 30 days, while those for 2027 also show improvement over the same period.
NVO Estimate Movement
Image Source: Zacks Investment Research
The Zacks Consensus Estimate for Amgen’s 2026 sales and EPS implies a year-over-year increase of 3% and 1.7%, respectively. AMGN’s EPS estimates have been trending upward over the past 30 days for both 2026 and 2027.
AMGN Estimate Movement
Image Source: Zacks Investment Research
Price Performance and Valuation of NVO & AMGN
Year to date, shares of NVO have lost 13.1%, while those of AMGN have gained 2.7%. In comparison, the industry has returned 2.3%, as seen in the chart below.
Image Source: Zacks Investment Research
From a valuation standpoint, Amgen is more expensive than Novo Nordisk, going by the price/earnings ratio. NVO’s shares currently trade at 12.80 times forward earnings, lower than 14.76 for AMGN.
However, Amgen currently looks like the better pick, supported by a more diversified business across several therapeutic areas. This broader revenue base offers greater resilience than Novo Nordisk’s more concentrated GLP-1-driven model. At the same time, Amgen still has meaningful exposure to the high-growth obesity market through its investigational candidate, MariTide. If successfully developed and approved, MariTide could allow Amgen to penetrate a massive obesity market opportunity while differentiating itself from weekly injectable therapies.
By contrast, Novo Nordisk remains the GLP-1 market leader, but its dominance is increasingly under pressure from Eli Lilly and other biotech players developing next-generation obesity drugs, including Amgen. NVO also faces serious operational and execution risks, including pricing pressure, softer prescription trends, reduced coverage, manufacturing and commercial spending needs, and gradual exclusivity losses in select markets. These challenges cloud near-term visibility, making it prudent for investors to avoid NVO until a clearer recovery path emerges.
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Novo Nordisk vs. Amgen: Which Pharma Stock Is the Better Buy?
Key Takeaways
Novo Nordisk (NVO - Free Report) and Amgen (AMGN - Free Report) are both global healthcare heavyweights with the scale, financial strength and research depth needed to turn scientific innovation into blockbuster drugs. Each company has built a reputation for durable franchises, strong pricing power and steady demand across critical treatment areas, making both stocks compelling long-term plays in the pharma sector.
Novo Nordisk is widely recognized as the market leader in the GLP-1 space, marketing its semaglutide drugs under brand names Ozempic (pre-filled pen and oral tablet) and Rybelsus (oral tablet) for type II diabetes (T2D), and Wegovy (injection and pill) for chronic weight management. Amgen, meanwhile, brings a more diversified portfolio across oncology, cardiovascular (CV) disease, inflammation, bone health and rare disease markets. It has some key pipeline assets, with a focus on the lead obesity candidate, MariTide.
That sets up a strong head-to-head debate: should investors favor Novo Nordisk’s concentrated exposure to the fast-growing GLP-1 market, or Amgen’s broader, more balanced biotech model with income-friendly characteristics? For investors weighing growth, resilience and risk, this pharma faceoff offers a timely look at two very different paths to long-term returns.
Let's examine the fundamentals of the two stocks to make a prudent choice.
The Case for NVO Stock
Novo Nordisk has achieved tremendous success in the cardiometabolic treatment space, driven primarily by Ozempic, Rybelsus and Wegovy. As of 2025-end, Novo Nordisk remained the market leader with a total GLP-1 volume market share of 54.6% globally across diabetes and obesity care.
Novo Nordisk is pursuing new indications for its semaglutide drugs, including CV and other indications. In 2025, Rybelsus became the first oral therapy approved in the United States to lower the risk of major adverse CV events in high-risk T2D patients, regardless of prior CV history. Wegovy’s label includes CV, HFpEF and osteoarthritis indications, while Ozempic remains the only GLP-1 approved to slow kidney disease and reduce CV death in patients with diabetes. Higher-dose Wegovy injections have been approved in the United States and the EU, expanding its portfolio and enabling the company to tailor treatment options better to meet the diverse needs and preferences of obesity patients. NVO is also seeking to expand Ozempic’s label to include peripheral artery disease.
In late December, the FDA also approved NVO’s 25 mg oral semaglutide (Wegovy pill) for obesity and CV disease, which was subsequently launched in early January. The FDA recently approved an oral version of Ozempic (1.5 mg, 4 mg and 9 mg) for adult T2D patients, which was subsequently launched in the United States. A supplemental application for a higher 25 mg tablet is also under review, with a regulatory decision expected by the end of 2026. Novo Nordisk also intends to seek regulatory approval for both Rybelsus and oral Ozempic in children and adolescents aged 10 to 17 years with T2D in the United States and the EU in the second half of 2026.
Novo Nordisk is advancing its next-generation obesity pipeline. It has submitted a regulatory filing seeking the approval of CagriSema injection, a follow-up drug to Wegovy, for obesity. Meanwhile, its mid-stage asset, amycretin, has shown strong weight-loss efficacy in a phase II study and is slated to enter phase III soon. The company has bolstered its pipeline through several major collaborations and acquisition deals.
Beyond GLP-1s, NVO is building its Rare Disease franchise, advancing Mim8 in hemophilia A, and securing both EU and U.S. approvals for Alhemo to treat hemophilia A and B, with or without inhibitors. Meanwhile, the FDA has granted accelerated approval for Wegovy in treating MASH with fibrosis. Novo Nordisk and rival Eli Lilly (LLY - Free Report) have also introduced multiple price cuts in response to pressure from the U.S. government during 2025 and 2026 to improve patient access to GLP-1 medicines.
Despite the recent wins, Novo Nordisk is far from being out of the woods yet. It has been facing increasing competition from Eli Lilly, which markets its tirzepatide (GLP-1) medicines as Mounjaro for T2D and Zepbound for obesity. Despite being on the market for just over three years, these drugs have become LLY’s key top-line drivers. Lilly recently secured FDA approval of its oral GLP-1 drug, orforglipron, for adults with obesity or overweight with weight-related medical problems, marketed under the brand name Foundayo. The drug competes directly with NVO’s Wegovy pill.
Although Novo Nordisk’s post-first-quarter guidance raise offered some reassurance, the bigger picture remains cautious — management still expects both sales and operating profit to decline in 2026, underscoring weak core momentum and mounting structural challenges. The modestly improved outlook reflects stronger GLP-1 demand, broader adoption of obesity treatments and ongoing Wegovy launches. However, these positives are being offset by U.S. pricing pressure, softer injectable GLP-1 prescription trends, reduced Medicaid obesity coverage, intensifying competition from Eli Lilly, “Most Favored Nation” pricing agreement, gradual semaglutide exclusivity losses in select markets and elevated spending on R&D, manufacturing and commercial expansion.
The Case for AMGN Stock
Amgen’s diverse portfolio and global reach position it well in a changing pharma landscape. Key medicines like Repatha, Evenity and Blincyto, as well as newer medicines like Tavneos, Tezspire, and Imdelltra, are driving sales, more than offsetting declining revenues from oncology biosimilars and mature products like Enbrel. New biosimilar launches are also contributing to top-line growth.
The 2023 acquisition of Horizon Therapeutics has significantly expanded Amgen's rare disease business by adding several rare disease drugs, including Tepezza, Krystexxa and Uplizna, to its portfolio. Amgen is also pursuing label expansions for its marketed drugs to broaden their approved uses and expand the addressable patient population. Approval for the expanded use of these drugs can potentially drive further top-line growth.
Amgen’s key pipeline candidate is MariTide, a GIPR/GLP-1 receptor, which is being evaluated for T2D, obesity and obesity-related conditions as part of its comprehensive MARITIME phase III program. Amgen has nine global phase III studies underway with MariTide in obesity, and other obesity-related conditions like obstructive sleep apnea, cardiovascular disease and heart failure. Three phase III studies of MariTide in T2D will be initiated in 2026.
Unlike the currently marketed obesity drugs like Eli Lilly’s Zepbound and Novo Nordisk’s Wegovy, which require weekly injections, MariTide is being tested for monthly dosing. A less frequent dosing regimen is expected to reduce treatment burden and thereby boost patient adherence. In prior clinical studies, the candidate has shown predictable and sustained weight loss and a meaningful impact on cardiometabolic parameters.
Beyond obesity, Amgen has promising late-stage pipeline drugs across several therapeutic areas, which represent significant commercial potential. These include olpasiran (for atherosclerotic CV disease), xaluritamig (metastatic castrate-resistant prostate cancer), daxdilimab (primary discoid lupus erythematosus) and dazodalibep (Sjögren’s disease).
Amgen also boasts a strong biosimilars portfolio, which includes Bekemv (biosimilar of AstraZeneca’s Soliris), Wezlana (J&J’s Stelara) and Pavblu (Regeneron’s Eylea). It is also developing biosimilar versions of blockbuster oncology drugs like Bristol Myers’ Opdivo, Merck’s Keytruda and Roche’s Ocrevus in phase III studies.
However, pricing headwinds and competitive pressure are negatively impacting the sales of many products. Sales of best-selling drugs, Prolia and Xgeva, are expected to decline in the upcoming quarters due to generic erosion following the loss of patent protection.
How Do Estimates Compare for NVO & AMGN?
The Zacks Consensus Estimate for Novo Nordisk’s 2026 sales and earnings per share (EPS) implies a year-over-year decline of around 3.6% and 12.6%, respectively. EPS estimates for 2026 have been trending upward over the past 30 days, while those for 2027 also show improvement over the same period.
NVO Estimate Movement
The Zacks Consensus Estimate for Amgen’s 2026 sales and EPS implies a year-over-year increase of 3% and 1.7%, respectively. AMGN’s EPS estimates have been trending upward over the past 30 days for both 2026 and 2027.
AMGN Estimate Movement
Price Performance and Valuation of NVO & AMGN
Year to date, shares of NVO have lost 13.1%, while those of AMGN have gained 2.7%. In comparison, the industry has returned 2.3%, as seen in the chart below.
From a valuation standpoint, Amgen is more expensive than Novo Nordisk, going by the price/earnings ratio. NVO’s shares currently trade at 12.80 times forward earnings, lower than 14.76 for AMGN.
NVO vs. AMGN: Which Stock Holds the Edge?
Novo Nordisk and Amgen carry a Zacks Rank #3 (Hold) each at present, which makes choosing one stock a difficult task. You can see the complete list of today’s Zacks #1 Rank (Strong Buy) stocks here.
However, Amgen currently looks like the better pick, supported by a more diversified business across several therapeutic areas. This broader revenue base offers greater resilience than Novo Nordisk’s more concentrated GLP-1-driven model. At the same time, Amgen still has meaningful exposure to the high-growth obesity market through its investigational candidate, MariTide. If successfully developed and approved, MariTide could allow Amgen to penetrate a massive obesity market opportunity while differentiating itself from weekly injectable therapies.
By contrast, Novo Nordisk remains the GLP-1 market leader, but its dominance is increasingly under pressure from Eli Lilly and other biotech players developing next-generation obesity drugs, including Amgen. NVO also faces serious operational and execution risks, including pricing pressure, softer prescription trends, reduced coverage, manufacturing and commercial spending needs, and gradual exclusivity losses in select markets. These challenges cloud near-term visibility, making it prudent for investors to avoid NVO until a clearer recovery path emerges.