The global biosimilars market
is set to witness a CAGR of ~15% in the next 5 years. Impending
patent expiry of blockbuster biologics, cost containment strategies by
governments and payers, rising demand for affordable alternatives for costly
biologics, strong regulatory support and clear guidelines, and increased
physician and patient acceptance are some of the key factors driving the
biosimilars market.
Biosimilars are
biologic medical products that are highly similar to an already approved
original biologic (reference product), with no clinically meaningful
differences in safety, purity, and effectiveness. The development of
biosimilars is complex because, like all biologics, it involves use of living
cells and complex manufacturing processes. Therefore, while biosimilars are
similar to the reference biologic, they are not identical. The manufacturer
must perform an extensive analytical, preclinical, and clinical evaluation to
demonstrate similarity. Biosimilars are not just generic alternatives to
expensive biologics; instead, they are a viable and reasonable cost alternative
to the original biologic, particularly when the reference product's patent has
expired. Biosimilars are widely used in the treatment and management of chronic
and life-threatening diseases, such as cancer, diabetes, and autoimmune
diseases. They help improve access to advanced therapies available globally for
patients.
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Impending patent
expiry of blockbuster biologics to drive market growth
The impending
patent expiries of best-selling biologics is a key factor driving growth of the
biosimilars market. A major opportunity for cost savings remains untapped, as
many high-value biologics nearing the end of patent protection and exclusivity
still lack biosimilar development, delaying broader market competition and
affordability. These revenue-generating biologics will be losing exclusivity
and allowing biosimilar manufacturers to introduce products at lower costs in
the biopharmaceutical market. This leads to competitive pricing, increases the
number of patients receiving access to biosimilars, and reduction in overall
healthcare costs. With most top-selling biologics nearing, if not already
passed, patent expiry, companies are investing into biosimilars to take benefit
of this opportunity. Regulators have also promoted a favorable environment for
biosimilars during this timeframe by updating their approval pathways, leading
to an overall acceleration of biosimilar entry into the market when the patent
expires.
Strategic
partnerships and market consolidation – A key market trend
Partnerships and
market consolidation is a key trend shaping this market as this to decrease
development costs, share risks, and launch products in a timely manner.
Partnerships involving global pharmaceutical companies and local firms,
contract manufacturers/developers, and biotech firms allows them to combine
their abilities which helps to gain advanced technology, knowledge of the
regulatory pathway, and existing infrastructure network for distribution. For
instance, in May 2025 Alvotech expanded its biosimilar partnership with Advanz
Pharma and added 3 new biosimilar candidates. Similarly, in July 2024, Evotec
SE extended its biosimilar strategic partnership with Sandoz. Furthermore, the
mergers and acquisitions taking place in the biosimilar marketplace are
facilitating consolidation in the competitive landscape, enabling companies to
scale operations and diversify their portfolios. Thus, partnerships can expand
their worldwide reach, streamline production processes and support
commercialization in the competitive and regulated biosimilar sector.
Competitive
Landscape Analysis
The global
biosimilars market is marked by the presence of established and emerging market
players such as Sandoz Group AG, Pfizer Inc., Amgen Inc., Teva
Pharmaceuticals, Inc., Biocon, Eli Lilly and Company, Celltrion Inc.,
Fresenius SE & Co. KGaA, Samsung Bioepis, and Dr.
Reddy’s Laboratories Ltd.; among others. Some of the key
strategies adopted by market players include new product development, strategic
partnerships and collaborations, and geographic expansion.
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Global
Biosimilars Market Segmentation
This report by
Medi-Tech Insights provides the size of the global biosimilars market at
the regional- and country-level from 2023 to 2030. The report further
segments the market based on product, application, and manufacturing type.
Market Size
& Forecast (2023-2030), By Product, USD Million
- Monoclonal Antibodies (mAbs)
- Insulin
- Granulocyte-Colony Stimulating Factor
(G-CSF)
- Erythropoietin
- Human Growth Hormone (hGH)
- Interferons
- Others
Others Market
Size & Forecast (2023-2030), By Application, USD Million
- Oncology
- Autoimmune Diseases
- Diabetes
- Blood Disorders
- Growth Hormone Deficiency
- Infectious Diseases
- Others
Market Size
& Forecast (2023-2030), By Manufacturing Type, USD Million
- In-house Manufacturing
- Contract Manufacturing
Market Size
& Forecast (2023-2030), By Region, USD Million
- North America
- US
- Canada
- Europe
- UK
- Germany
- France
- Italy
- Spain
- Rest of Europe
- Asia Pacific
- China
- India
- Japan
- Rest of Asia Pacific
- Latin America
- Middle East & Africa
About Medi-Tech
Insights
Medi-Tech Insights
is a healthcare-focused business research & insights firm. Our clients
include Fortune 500 companies, blue-chip investors & hyper-growth
start-ups. We have completed 100+ projects in Digital Health, Healthcare IT,
Medical Technology, Medical Devices & Pharma Services in the areas of
market assessments, due diligence, competitive intelligence, market sizing and
forecasting, pricing analysis & go-to-market strategy. Our methodology
includes rigorous secondary research combined with deep-dive interviews with
industry-leading CXO, VPs, and key demand/supply side decision-makers.
Contact:
Ruta Halde
Associate, Medi-Tech Insights
+32 498 86 80 79
info@meditechinsights.com
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