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Insights

GLP-1s: Still early in the growth story

Lin-Lawrence
Lawrence Lin
CFA, Senior Portfolio Manager and Senior Analyst, Equity Research

The GLP-1 market continues to expand rapidly yet remains in the early stages of growth. The GLP-1 market is no longer simply a weight-loss story. It is evolving into a broad cardiometabolic platform with expanding indications, improving formulations and a long runway for deeper penetration.

While the category has already reached significant scale, we believe investors may still be underestimating the durability of growth as innovation broadens use cases, improves adherence and expands access across patient segments.

What investors may still be underestimating

  • Penetration remains low relative to the addressable population. The GLP-1 market has grown at over 40% annually and now exceeds $80 billion. Despite approximately 11 million US patients currently receiving treatment, significant runway for growth remains, as roughly 40% of the US population is overweight and may be eligible to benefit from GLP-1 therapy.
  • Future growth may come from a broader range of patients, not just obesity patients. The clinical utility of GLP-1 therapies continues to expand beyond their primary uses in type 2 diabetes and obesity. Adoption is growing in areas such as obstructive sleep apnoea (OSA), where weight loss can significantly improve outcomes, while evidence of cardiovascular benefits has broadened their use among at-risk patients. The expanding range of indications may support continued growth in the addressable market over time.
  • Oral therapies may expand the market, not simply replace injectables. New oral therapies are broadening adoption, with 8 out of 10 oral GLP-1 users new to the category.2
  • Untapped global opportunity. Globally, the number of adults living with obesity is projected to rise from 810 million in 2020 to 1.53 billion by 2035, according to the World Obesity Foundation, underscoring the scale of unmet medical need and the potential long-term runway for effective treatments. While current therapies have delivered compelling outcomes, opportunities for further improvement remain, supporting continued innovation and long-term market expansion.

Collectively, these trends suggest the market’s opportunity extends well beyond weight loss alone. As new indications emerge, adoption broadens and more patients gain access to treatment, the number of patients receiving GLP-1 therapies continues to grow across both obesity and type 2 diabetes.

Market opportunity

The GLP-1 story is expanding beyond its diabetes foundation, with growing obesity use becoming a major driver of the industry’s long-term growth trajectory. This shift in utilisation helps explain why many investors view the category as a compelling multi-year growth opportunity.

The broadening use of GLP-1 therapies is evident in patient enrolment trends, which continue to reach new highs across key treatment categories.

GLP-1 patient adoption continues to climb

US patients on GLP-1 therapy (millions)

graph

Source: FAIR Health, Inc. and Columbia Threadneedle Investments analysis. Data as of 31 July 2026.

Injectables lead, orals broaden adoption

Injectable GLP-1 therapies continue to dominate the market, supported by their superior efficacy and overall risk-benefit profile. Current injectable products generally deliver greater weight loss than oral alternatives, making them the preferred option for patients seeking substantial weight reduction.

Oral therapies, however, address an important unmet need. By eliminating injections, they offer greater convenience and may appeal to patients reluctant to self-administer injections. Orals may also be well suited to individuals seeking more modest weight loss or maintenance after achieving their target weight. Because oral therapies are relatively new, physicians and patients are still determining where they fit most effectively within the treatment landscape. Over time, oral GLP-1 therapies may support broader adoption and greater patient persistence, extending the runway for category growth.

The key question is not whether oral therapies will replace injectables, but how they will be positioned alongside them. We view oral GLP-1s as expanding the addressable market rather than materially cannibalising injectable demand.

Oral GLP-1s gain share in the obesity and total market

graph 2

Source: Fierce Pharma; Columbia Threadneedle Investments analysis. Data as of 4 September 2026.

GLP-1s’ growth runway remains long

The GLP-1 market has emerged as one of largest pharmaceutical opportunities in history, driven by demand across type 2 diabetes, obesity and a growing list of related indications. Despite declining prices, industry revenues continue to grow at a rapid pace as patient adoption rises. Yet penetration remains remarkably low compared to the potential addressable market. Despite rapid growth, GLP-1 therapies remain relatively underpenetrated in the US, while adoption rates in international markets are even lower. While the market has experienced high double-digit annual growth in recent years, consensus forecasts anticipate growth moderating to approximately 14% annually over the next five years. We believe those expectations may prove conservative. Given the pipeline of improved drugs on the horizon, continued innovation, broader clinical applications and deeper market penetration could support faster growth than is currently reflected in market estimates. The table below highlights the extent of the opportunity, comparing current penetration levels with the market’s substantial remaining growth potential.

GLP-1 market consensus estimates point to continued expansion

2026
2027
2028
2029
2030
2031
Total GLP-1 class
98.6
120.7
138.4
158.9
174.2
190.6
22.5%
14.6%
14.8%
9.7%
9.4%

Source: Bloomberg L.P., Columbia Threadneedle Investments analysis. Data as of 4 September 2026.

Execution and innovation are shaping competitive leadership

Competitive advantage in GLP-1s is increasingly being defined by more than first-mover status. Scale, manufacturing reliability, breadth of indications, clinical differentiation, payer access, pricing strategy and pipeline depth are all becoming critical determinants of long-term share. The market share impact of these competitive dynamics is already evident. As shown below, Lilly has steadily gained share at the expense of its closest competitor.

Lilly currently holds approximately 62% of the GLP-1 market, compared with roughly 38% for Novo Nordisk, and recent competitive trends suggest the company is well positioned to maintain, and potentially extend, its leadership position. Lilly’s portfolio, anchored by Mounjaro and Zepbound, has benefited from strong clinical efficacy, broad demand and improved product availability. Looking ahead, the company is expected to seek regulatory approval for retatrutide, a next-generation GIP/GLP-1/glucagon therapy, in 2027. While numerous competitors are advancing obesity and metabolic disease treatments, Lilly’s pipeline remains among the deepest in the industry, supported by decades of investment and expertise in this therapeutic area.

Lilly extends its lead in the GLP-1 market

graph 4

Source: Flagship drug market includes Mounjaro, Zepbound, Foundayo, Ozempic, Wegovy and Oral Wegovy. Fierce Pharma; Columbia Threadneedle Investments analysis. Data as of 17 July 2026.

Lilly has established a leadership position through strong commercial execution and a growing portfolio of therapies, including Mounjaro, Zepbound and recently approved next-generation products (Foundayo). While Novo Nordisk pioneered the category with Ozempic and Wegovy, Lilly has gained share by demonstrating a better risk/benefit profile, expanding manufacturing capacity, improving product availability and advancing a broad clinical development programme.

Compounded GLP-1 therapies gained traction during branded-drug shortages by offering greater availability and lower prices. An estimated one million patients remain on compounded products, which typically cost $150 to $285 per month. However, as branded supply has improved and manufacturers have lowered prices, the gap in cost and availability has narrowed, reducing the relative appeal of compounded alternatives.

The table below compares the current pricing and access landscape across leading obesity and diabetes therapies.

Comparative pricing across market leaders

Primary usage
Company
Product
WAC price(Wholesale acquisition cost, per month)
Lowest direct-to-consumer price (per month)
Oral obesity
Lilly
Novo Nordisk
Foundayo
Wegovy pill
$649
$1,349
$149 (0.8 mg)
$149 (1.5 mg)
Injectable obesity
Lilly
Novo Nordisk
Zepbound
Wegovy pen
$1,086
$1,349
$299 (2.5 mg)
$199 (0.25, 0.5 mg*)
Type 2 diabetes
Lilly
Novo Nordisk
Mounjaro
Ozempic
$1,077
$1,028
$499 (2.5–15 mg)
$149 (0.25, 0.5 mg**)

* First 2 months for new patients; then rises to $299/month.
**First 2 months for new patients; then rises to $349/month.

Source: Company reports and Columbia Threadneedle Investments analysis. Data as of 31 July 2026.

Pipeline innovation points to a longer growth runway

Current GLP-1 drugs have delivered impressive clinical and commercial success, but meaningful opportunities for improvement remain. The next generation of therapies are focused on improving tolerability, preserving lean muscle mass, increasing weight-loss efficacy, reducing dosing frequency and expanding oral treatment options. While recent advances have been remarkable, they are the product of decades of research and innovation.

The first GLP-1 therapy, Lilly’s exenatide, was introduced in 2005 and required twice-daily dosing while offering modest weight-loss benefits and limited tolerability. Today’s products represent a significant step forward, and we expect ongoing innovation to further improve efficacy, convenience and patient outcomes.

Several late-stage candidates warrant close attention, including Lilly’s eloralintide, long-acting tirzepatide and retatrutide, Novo’s CagriSema, Amgen’s MariTide and Kailera’s oral ribupatide. These programmes could improve efficacy, convenience and tolerability, further expanding the addressable market.

Risks to monitor

The category’s growth trajectory is not without risk. Greater competition could intensify pricing pressure, while reimbursement changes may affect patient access and affordability. Adoption in new indications could also develop more slowly than expected, and next-generation therapies may alter the competitive landscape. Regulatory setbacks, manufacturing constraints and product-supply disruptions remain additional risks for companies operating in the market.

The bottom line

Despite remarkable growth, the GLP-1 opportunity remains far from fully realised. Low market penetration, expanding clinical applications and continued innovation could support category growth for years to come. As innovation continues and adoption broadens, GLP-1s have the potential to deliver better patient outcomes while creating durable opportunities for well-positioned companies.

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1 Growth rate of over 40% represents a five-year compounded annual growth rate.

2 Novo Nordisk A/S, based on Q2 FY2026 earnings call, 5 August 2026.

Important information

For use by professional clients and/or equivalent investor types in your jurisdiction (not to be used with or passed on to retail clients). For marketing purposes.

This document is intended for informational purposes only and should not be considered representative of any particular investment. This should not be considered an offer or solicitation to buy or sell any securities or other financial instruments, or to provide investment advice or services. Investing involves risk including the risk of loss of principal. Your capital is at risk. Market risk may affect a single issuer, sector of the economy, industry or the market as a whole. The value of investments is not guaranteed, and therefore an investor may not get back the amount invested. International investing involves certain risks and volatility due to potential political, economic or currency fluctuations and different financial and accounting standards. The securities included herein are for illustrative purposes only, subject to change and should not be construed as a recommendation to buy or sell. Securities discussed may or may not prove profitable. The views expressed are as of the date given, may change as market or other conditions change and may differ from views expressed by other Columbia Threadneedle Investments (Columbia Threadneedle) associates or affiliates. Actual investments or investment decisions made by Columbia Threadneedle and its affiliates, whether for its own account or on behalf of clients, may not necessarily reflect the views expressed. This information is not intended to provide investment advice and does not take into consideration individual investor circumstances. Investment decisions should always be made based on an investor’s specific financial needs, objectives, goals, time horizon and risk tolerance. Asset classes described may not be suitable for all investors. Past performance does not guarantee future results, and no forecast should be considered a guarantee either. Information and opinions provided by third parties have been obtained from sources believed to be reliable, but accuracy and completeness cannot be guaranteed. This document and its contents have not been reviewed by any regulatory authority.

In Australia: Issued by Threadneedle Investments Singapore (Pte.) Limited [“TIS”], ARBN 600 027 414. TIS is exempt from the requirement to hold an Australian financial services licence under the Corporations Act 2001 (Cth) and relies on Class Order 03/1102 in respect of the financial services it provides to wholesale clients in Australia. This document should only be distributed in Australia to “wholesale clients” as defined in Section 761G of the Corporations Act. TIS is regulated in Singapore (Registration number: 201101559W) by the Monetary Authority of Singapore under the Securities and Futures Act (Chapter 289), which differ from Australian laws.

In Singapore: Issued by Threadneedle Investments Singapore (Pte.) Limited, 3 Killiney Road, #07-07, Winsland House 1, Singapore 239519, which is regulated in Singapore by the Monetary Authority of Singapore under the Securities and Futures Act (Chapter 289). Registration number: 201101559W. This advertisement has not been reviewed by the Monetary Authority of Singapore.

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In the Middle East: This document is distributed by Columbia Threadneedle Investments (ME) Limited, which is regulated by the Dubai Financial Services Authority (DFSA). For Distributors: This document is intended to provide distributors with information about Group products and services and is not for further distribution. For Institutional Clients: The information in this document is not intended as financial advice and is only intended for persons with appropriate investment knowledge and who meet the regulatory criteria to be classified as a Professional Client or Market Counterparties and no other Person should act upon it.

This document may be made available to you by an affiliated company which is part of the Columbia Threadneedle Investments group of companies: Columbia Threadneedle Management Limited in the UK; Columbia Threadneedle Netherlands B.V., regulated by the Dutch Authority for the Financial Markets (AFM), registered No. 08068841.

Columbia Threadneedle Investments is the global brand name of the Columbia and Threadneedle group of companies. © 2026 Columbia Threadneedle. All rights reserved.

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Important information

For use by professional clients and/or equivalent investor types in your jurisdiction (not to be used with or passed on to retail clients). For marketing purposes.

This document is intended for informational purposes only and should not be considered representative of any particular investment. This should not be considered an offer or solicitation to buy or sell any securities or other financial instruments, or to provide investment advice or services. Investing involves risk including the risk of loss of principal. Your capital is at risk. Market risk may affect a single issuer, sector of the economy, industry or the market as a whole. The value of investments is not guaranteed, and therefore an investor may not get back the amount invested. International investing involves certain risks and volatility due to potential political, economic or currency fluctuations and different financial and accounting standards. The securities included herein are for illustrative purposes only, subject to change and should not be construed as a recommendation to buy or sell. Securities discussed may or may not prove profitable. The views expressed are as of the date given, may change as market or other conditions change and may differ from views expressed by other Columbia Threadneedle Investments (Columbia Threadneedle) associates or affiliates. Actual investments or investment decisions made by Columbia Threadneedle and its affiliates, whether for its own account or on behalf of clients, may not necessarily reflect the views expressed. This information is not intended to provide investment advice and does not take into consideration individual investor circumstances. Investment decisions should always be made based on an investor’s specific financial needs, objectives, goals, time horizon and risk tolerance. Asset classes described may not be suitable for all investors. Past performance does not guarantee future results, and no forecast should be considered a guarantee either. Information and opinions provided by third parties have been obtained from sources believed to be reliable, but accuracy and completeness cannot be guaranteed. This document and its contents have not been reviewed by any regulatory authority.

In Australia: Issued by Threadneedle Investments Singapore (Pte.) Limited [“TIS”], ARBN 600 027 414. TIS is exempt from the requirement to hold an Australian financial services licence under the Corporations Act 2001 (Cth) and relies on Class Order 03/1102 in respect of the financial services it provides to wholesale clients in Australia. This document should only be distributed in Australia to “wholesale clients” as defined in Section 761G of the Corporations Act. TIS is regulated in Singapore (Registration number: 201101559W) by the Monetary Authority of Singapore under the Securities and Futures Act (Chapter 289), which differ from Australian laws.

In Singapore: Issued by Threadneedle Investments Singapore (Pte.) Limited, 3 Killiney Road, #07-07, Winsland House 1, Singapore 239519, which is regulated in Singapore by the Monetary Authority of Singapore under the Securities and Futures Act (Chapter 289). Registration number: 201101559W. This advertisement has not been reviewed by the Monetary Authority of Singapore.

In Hong Kong: Issued by Threadneedle Portfolio Services Hong Kong Limited 天利投資管理香港有限公司. Unit 3004, Two Exchange Square, 8 Connaught Place, Hong Kong, which is licensed by the Securities and Futures Commission (“SFC”) to conduct Type 1 regulated activities (CE:AQA779). Registered in Hong Kong under the Companies Ordinance (Chapter 622), No. 1173058.

In Japan: Issued by Columbia Threadneedle Investments Japan Co., Ltd. Financial Instruments Business Operator, The Director-General of Kanto Local Finance Bureau (FIBO) No.3281, and a member of Investment Management Association of Japan and Type II Financial Instruments Firms Association.

In the UK: Issued by Threadneedle Asset Management Limited, No. 573204 and/or Columbia Threadneedle Management Limited, No. 517895, both registered in England and Wales and authorised and regulated in the UK by the Financial Conduct Authority.

In the EEA: Issued by Threadneedle Management Luxembourg S.A., registered with the Registre de Commerce et des Sociétés (Luxembourg), No. B 110242 and/or Columbia Threadneedle Netherlands B.V., regulated by the Dutch Authority for the Financial Markets (AFM), registered No. 08068841.

In Switzerland: Issued by Threadneedle Portfolio Services AG, Registered address: Claridenstrasse 41, 8002 Zurich, Switzerland.

In the Middle East: This document is distributed by Columbia Threadneedle Investments (ME) Limited, which is regulated by the Dubai Financial Services Authority (DFSA). For Distributors: This document is intended to provide distributors with information about Group products and services and is not for further distribution. For Institutional Clients: The information in this document is not intended as financial advice and is only intended for persons with appropriate investment knowledge and who meet the regulatory criteria to be classified as a Professional Client or Market Counterparties and no other Person should act upon it.

This document may be made available to you by an affiliated company which is part of the Columbia Threadneedle Investments group of companies: Columbia Threadneedle Management Limited in the UK; Columbia Threadneedle Netherlands B.V., regulated by the Dutch Authority for the Financial Markets (AFM), registered No. 08068841.

Columbia Threadneedle Investments is the global brand name of the Columbia and Threadneedle group of companies. © 2026 Columbia Threadneedle. All rights reserved.

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