This report provides an assessment of trends in the global biosimilar market, with an emphasis on market and competitive dynamics in the US and Europe.
The 2025 edition builds on Alira Health’s foundational 2024 analysis, updating all data and forecasts with the latest 2025 figures. It offers a consistent, year-over-year view of global biosimilar activity—from product launches to market access trends—showing how the biosimilars landscape continues to evolve worldwide.
This report provides an assessment of trends in the global biosimilar market, with an emphasis on market and competitive dynamics in the US and Europe.
The 2025 edition builds on Alira Health’s foundational 2024 analysis, updating all data and forecasts with the latest 2025 figures. It offers a consistent, year-over-year view of global biosimilar activity — from product launches to market access trends — showing how the biosimilars landscape continues to evolve worldwide.
With loss of exclusivity for the first blockbuster biologics, patent-protected drugs that reached billion-dollar sales, the industry witnessed the emergence of biosimilars, which are highly similar versions of already approved biologics. The introduction of biosimilars marked a significant evolution in healthcare, offering comparable therapeutic benefits at lower costs. This promise of expanded patient access and reduced financial burden on health systems is already manifesting. The global biosimilars market has grown substantially over the last five years: in 2024, it reached $30.3 billion, growing at a compound annual growth rate (CAGR) of 14% since 2020.
The global biosimilars market has greatly matured and expanded in the last few years, with the European Union and the United States leading this growth. The American biosimilars market grew at a CAGR of 11%, from $7.1 billion in 2020 to $10.9 billion in 2024, fueled by regulatory advancements including the Inflation Reduction Act and updated FDA guidance on biosimilar interchangeability. As the first region to establish a biosimilar regulatory framework, Europe remains a leader in the global market, growing at 13% each year from a market size of $8.9 billion in 2020 to $14.6 billion in 2024. The region’s supportive regulatory environment and extensive experience with biosimilar approvals have allowed it to maintain a dominant market position. Emerging biosimilar markets in Latin America and the Middle East and Africa have exhibited strong growth potential at a CAGR of over 40% from 2020 to 2024. Like many other markets, this growth is driven by the need to reduce healthcare costs and improve access to biologics treatments.
The biosimilars market is currently dominated by large pharmaceutical companies such as Sandoz, Pfizer, and Amgen, which together control 50% of the global market. These companies leverage their extensive research and development capabilities and global reach to maintain a competitive edge. Significant deal activity, including mergers and acquisitions as well as licensing agreements, has also shaped the market, allowing companies to expand their biosimilar portfolios and accelerate time to market.
The biosimilars market is poised for continued growth, projected to exceed $76 billion by 2029, driven by patent expirations, favorable regulatory environments, and an increasing number of biosimilar approvals. The entry of new players, particularly generics companies, will influence the market’s evolution because they may employ different business models to compete with established pharmaceutical firms. As the market matures even further, these dynamics will play a crucial role in determining the future landscape of biosimilars.
With loss of exclusivity for the first blockbuster biologics, patent-protected drugs that reached billion-dollar sales, the industry witnessed the emergence of biosimilars, which are highly similar versions of already approved biologics. The introduction of biosimilars marked a significant evolution in healthcare, offering comparable therapeutic benefits at lower costs. This promise of expanded patient access and reduced financial burden on health systems is already manifesting. The global biosimilars market has grown substantially over the last five years: in 2024, it reached $30.3 billion, growing at a compound annual growth rate (CAGR) of 14% since 2020.
The global biosimilars market has greatly matured and expanded in the last few years, with the European Union and the United States leading this growth. The American biosimilars market grew at a CAGR of 11%, from $7.1 billion in 2020 to $10.9 billion in 2024, fueled by regulatory advancements including the Inflation Reduction Act and updated FDA guidance on biosimilar interchangeability. As the first region to establish a biosimilar regulatory framework, Europe remains a leader in the global market, growing at 13% each year from a market size of $8.9 billion in 2020 to $14.6 billion in 2024. The region’s supportive regulatory environment and extensive experience with biosimilar approvals have allowed it to maintain a dominant market position. Emerging biosimilar markets in Latin America and the Middle East and Africa have exhibited strong growth potential at a CAGR of over 40% from 2020 to 2024. Like many other markets, this growth is driven by the need to reduce healthcare costs and improve access to biologics treatments.
The biosimilars market is currently dominated by large pharmaceutical companies such as Sandoz, Pfizer, and Amgen, which together control 50% of the global market. These companies leverage their extensive research and development capabilities and global reach to maintain a competitive edge. Significant deal activity, including mergers and acquisitions as well as licensing agreements, has also shaped the market, allowing companies to expand their biosimilar portfolios and accelerate time to market.
The biosimilars market is poised for continued growth, projected to exceed $76 billion by 2029, driven by patent expirations, favorable regulatory environments, and an increasing number of biosimilar approvals. The entry of new players, particularly generics companies, will influence the market’s evolution because they may employ different business models to compete with established pharmaceutical firms. As the market matures even further, these dynamics will play a crucial role in determining the future landscape of biosimilars.
This chapter provides a comprehensive overview of the global biosimilar ecosystem, outlining the evolution of biosimilars, their regulatory frameworks, and development pathways. It explores key stakeholders, market dynamics, and the growing role of biosimilars in improving patient access and reducing healthcare costs worldwide.
This chapter examines the evolution and expansion of the global biosimilar market, from its regulatory origins in the EU and US to its rapid worldwide growth. It explores key geographies, emerging markets, therapeutic areas, and the major trends, drivers, and challenges shaping the biosimilar industry’s future.
ARTICLE – 8 MIN. READ
ARTICLE – 11 MIN. READ
This chapter provides a comprehensive overview of the global biosimilar ecosystem, outlining the evolution of biosimilars, their regulatory frameworks, and development pathways. It explores key stakeholders, market dynamics, and the growing role of biosimilars in improving patient access and reducing healthcare costs worldwide.
ARTICLE – 8 MIN. READ
This chapter examines the evolution and expansion of the global biosimilar market, from its regulatory origins in the EU and US to its rapid worldwide growth. It explores key geographies, emerging markets, therapeutic areas, and the major trends, drivers, and challenges shaping the biosimilar industry’s future.
ARTICLE – 11 MIN. READ
This chapter analyzes the diverse landscape of companies shaping the biosimilar market, from large pharmaceutical corporations and generics manufacturers to biotech innovators and CDMOs. It explores the evolution of market participation, recent divestments, and the dominance of key players such as Sandoz, Pfizer, and Amgen.
This chapter explores how strategic partnerships, licensing agreements, and M&A have shaped the biosimilar industry’s evolution. It analyzes key deal trends since 2015—highlighting the surge in licensing and acquisition activity in 2021 and 2022, the growing involvement of generics companies, and landmark transactions.
ARTICLE – 13 MIN. READ
ARTICLE – 12 MIN. READ
This chapter analyzes the diverse landscape of companies shaping the biosimilar market, from large pharmaceutical corporations and generics manufacturers to biotech innovators and CDMOs. It explores the evolution of market participation, recent divestments, and the dominance of key players such as Sandoz, Pfizer, and Amgen.
ARTICLE – 13 MIN. READ
This chapter explores how strategic partnerships, licensing agreements, and M&A have shaped the biosimilar industry’s evolution. It analyzes key deal trends since 2015—highlighting the surge in licensing and acquisition activity in 2021 and 2022, the growing involvement of generics companies, and landmark transactions.
ARTICLE – 12 MIN. READ
The report outlook forecasts the next phase of biosimilar market growth, projecting the sector to reach $77 billion by 2029 with a 20% CAGR. It examines how upcoming patent expirations for major biologics will unlock new opportunities, reshape competition, and drive strategic shifts as generics and pharma companies pursue different business models to capture emerging market value.
ARTICLE – 8 MIN. READ
This chapter forecasts the next phase of biosimilar market growth, projecting the sector to reach $77 billion by 2029 with a 20% CAGR. It examines how upcoming patent expirations for major biologics will unlock new opportunities, reshape competition, and drive strategic shifts as generics and pharma companies pursue different business models to capture emerging market value.
ARTICLE – 4 MIN. READ
At Alira Health, we guide in CDMO selection and GMP-compliant facility design for successful commercialization of your biosimilar product. Discover how we help stakeholders navigate challenges, including navigating diverse regulatory pathways, managing complex clinical trials, and addressing pricing and market access barriers in the US, EU, and global markets.
At Alira Health, we guide in CDMO selection and GMP-compliant facility design for successful commercialization of your biosimilar product. Discover how we help stakeholders navigate challenges, including navigating diverse regulatory pathways, managing complex clinical trials, and addressing pricing and market access barriers in the US, EU, and global markets.
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This report provides an assessment of trends in the global biosimilar market, with an emphasis on market and competitive dynamics in the United States (US) and Europe.
We consider the legal and regulatory context that uniquely impacts the biosimilar space and expand on key players and their biosimilar-related licensing and mergers and acquisitions (M&A) activity.
This report includes Alira Health analysis that builds on proprietary datasets from IQVIA and Global Data. The report’s insights are largely based on Alira Health’s best estimates, and we cannot guarantee the accuracy of all the information presented herein. As such, data is subject to revision over time.
Market Analysis: Analyzed the global biosimilar industry based on historic product sales. Market projections build upon the analysis of product sales data, expected patent expirations, and key market drivers.
Biosimilar Deal Activity: Reviewed biosimilar-related transactions, including licensing, asset, and M&A deals, that were closed from 2015 to 2025 (last updated as of September 2025).
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