The Global Peptide Synthesis Market size is expected to reach USD 866.7 Mn by 2032, from USD 519.0 Mn in 2025, exhibiting a CAGR of 7.6% during the forecast period.
The peptide synthesis market has been witnessing consistent growth over the past few years, fueled by enhanced demand for peptide-based therapeutics, growing investments in pharmaceutical R&D, and advances in synthetic chemistry. Peptides are also being researched more and more in oncology, metabolic disorders, and infectious disease indications due to their specificity and good safety profiles. Growth of custom peptide services and automation of synthesis processes is also driving the market. In addition, solid-phase synthesis and liquid-phase synthesis methods are further increasing productivity and purity, and peptides are thus becoming more readily available for research and commercial use.
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Current Events |
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AI-Driven Peptide Design and Optimization Platforms |
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Enlargement of High-Capacity Automated Mass-Scale Peptide Production Manufacturing |
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Peptide synthesis market pipeline is healthy, propelled by increasing drug discovery activity and the rise of peptide therapeutic candidates. As of early 2025, there are more than 630 peptide-based clinical trials active, with over 80 peptides already approved in multiple indications—such as cancer, metabolic, and autoimmune disorders. This strong pipeline indicates increasing dependence on peptides as precision-targeted therapies.
Contract Development and Manufacturing Organizations (CDMOs) are central to this network. There are 75+ companies worldwide that provide peptide API manufacturing and associated services. These CDMOs facilitate scalable synthesis, purification, and regulatory assistance for sophisticated therapeutic peptides. Industry leaders such as Bachem, Thermo Fisher, Merck, GenScript, CordenPharma, and PolyPeptide Group own this pipeline, managing together early-stage and late-stage peptide projects.
Technological advancements are driving peptide pipeline throughput. Specifically, Cambrex (through Snapdragon Chemistry) introduced a liquid-phase peptide synthesis (LPPS) platform in September 2024, pairing batch reactors with continuous flow to minimize solvent usage and increase yields—a significant benefit for high-volume synthesis. In parallel, academic innovations like CreoPep, a deep-learning platform developed mid‑2025, facilitate label-free design of high-affinity peptides—efficiently guiding candidate selection early in the pipeline.
On the production side, firms such as Corden Pharma invested more than USD 526 million in early 2025 to construct a new GMP peptide production plant in Switzerland to increase capacity for research and commercial peptide production. Moreover, BioDuro established an automated SPPS-scale laboratory in early 2025 in Shanghai to facilitate greater throughput for commercial peptide API supply. In total, the pipeline for peptide synthesis is growing fast—with ongoing innovation in discovery as well as manufacturing—aided by an increasing CDMO ecosystem and disruptive technologies.
The market for peptide synthesis is dominated by a thick patent landscape with dominant players and focused innovators in possession of seminal intellectual property in technologies such as Liquid‑Phase Peptide Synthesis (LPPS) and enzymatic coupling. Companies such as Ajinomoto, Bachem, Eli Lilly, Jitsubo, Enzypep/Almac, Novozymes, and Exactmer dominate core LPPS and enzymatic approaches, with closely overlapping patent clusters forming thickets that restrict the competitors' freedom-to-operate in high-efficiency, continuous synthesis methods.
Although foundational LPPS patents such as Jitsubo’s early filings and Ajinomoto’s mid‑2010s filings are not yet expired—in fact many extend into the early 2030s—expiration of some in the late 2020s is expected to open opportunities for broader adoption. Similarly, key enzymatic synthesis patents (e.g. Enzypep’s 2008–2013 filings) are due to lapse between 2028 and 2033, which may enable entry by generic manufacturers or smaller players using these greener coupling routes.
Thematic filings for patents peaked from 2015 to 2025, indicating industry investment in patented technology such as continuous flow LPPS reactors, enzyme-engineered systems with increased substrate scope, and solvent-minimizing green processes. There are typical licensing partnerships—in the case of Bachem, enzyme-platforms have been licensed—and control over patents tends to rest with small innovators, while larger CMO and pharma companies maintain complementary IP for scale-up.
Filing is also emerging on AI-designed peptides and green synthesis technologies, with companies patenting on bio‑informatics‑based library generation and waste‑minimizing chemistry platforms. Patent analytics tools based on AI such as Patent Agent are also being patented to automate IP strategy in pharma R&D.
Overall, the patent environment remains protective and concentrated: competitors must carefully negotiate licensing or await expirations to access key innovations in LPPS or enzymatic peptide synthesis, while future generics entry is tied to expiry cycles and new licenses.
The global peptide synthesis market is expected to witness significant growth over the coming years owing to the rising demand from the pharmaceutical industry worldwide. Peptides have emerged as an important class of therapeutic molecules that offer several advantages over conventional small molecule drugs, such as high selectivity and potency. Several peptide-based drugs are already on the market for the treatment of cancer, metabolic disorders, cardiovascular diseases, and other chronic conditions.
Moreover, peptides can be customized and modified through chemical synthesis to improve their activity, selectivity, and bioavailability. With increasing focus on developing novel biotherapeutics, pharmaceutical companies are actively involved in peptide-based drug discovery and development programs. Peptide drugs currently under clinical trials or U.S. Food and Drug Administration review have demonstrated efficacy in conditions where conventional treatments have limitations.
Another key driver propelling the peptide synthesis market is the rising academic and industrial research in the areas of proteomics and genomics. Proteomics deals with the large-scale study of proteins, particularly their structures, functions, and interactions. It helps in a comprehensive understanding of physiological and pathological processes in living systems. Peptide synthesis plays a critical role in proteomics, as peptides serve as convenient surrogates for proteins in analytical methods and assay development. They are also used as signature tags for protein identification and biomarker discovery through mass spectrometry.
Genomics research involving the identification of protein-protein interactions and protein expression profiling also relies on customized peptide synthesis. With advancements in high-throughput techniques, the scope and scale of proteomics and genomics investigations have grown significantly in recent years. Major academic institutions and contract research organizations have set up core proteomics facilities to support multi-disciplinary research applying these ‘omics’ approaches. As these studies increasingly focus on clinical applications related to precision medicine, healthcare, and disease pathology, it will generate a persistent demand for specialized peptide synthesis services.
The market is witnessing new product launches catering to emerging proteomics and genomics applications such as specialized resin beads, novel linkers, and reagent kits for multiplex assays. This increasing adoption of proteomics and genomics technologies by research organizations is driving growth of the global peptide synthesis market.
The global peptide synthesis market is indeed witnessing a growing focus on customized peptides, which cater to specific research, therapeutic, and commercial needs. Custom peptides are tailor-made to specific sequences and modifications required by researchers and pharmaceutical companies. Here is an overview of why customized peptides are gaining prominence.
Reagents and consumables dominate the peptide synthesis market with a 56.2% share due to their recurring demand in every synthesis cycle. Each peptide production requires specific amino acids, coupling agents, and solvents, which must be replenished regularly. Unlike instruments, which are long-term assets, reagents are consumed with each batch. The growing number of research activities and peptide-based drug development increases their usage. Additionally, advancements in reagent efficiency and purity have boosted their adoption across labs and pharma companies.

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North America is expected to be the largest market for peptide synthesis during the forecast period, accounting for over 35.70% of the market share in 2025. North America has remained the dominant region in the global peptide synthesis market over the past decade. The presence of major pharmaceutical and biotechnology companies in the U.S. and Canada has fueled research and development activities in this field.
These companies are actively investing in developing novel peptide-based drugs and therapeutics. Furthermore, strong government funding for healthcare and life sciences research provides impetus to peptide-based drug discovery and drives regional market growth.
The pricing of synthesized peptides in North America is among the highest globally due to the advanced technologies and production capabilities of players in this region. For instance, most American companies offering peptide synthesis services employ sophisticated techniques like solid-phase peptide synthesis, which enable the production of complex peptides.
This sophisticated production comes at a premium but ensures the highest purity and yield for customers. Several North American companies also have extensive custom peptide libraries that allow academic researchers to screen millions of peptide sequences at once for their studies.
Asia Pacific market is expected to be the second-largest market for peptide synthesis, accounting for over 25.2% of the market share in 2025. Asia Pacific has emerged as the fastest-growing regional market for peptide synthesis in recent times on account of increasing investments by international manufacturers to tap into the opportunities in this region.
Countries like China, India, and South Korea have emerged as global hotspots for outsourced drug discovery and manufacturing activities due to the availability of a low-cost and highly skilled scientific workforce. Domestic players in Asia Pacific are gaining expertise in custom peptide synthesis, which is attracting several multinational pharmaceutical companies to outsource their peptide needs to this region.
Moreover, governments across Asia Pacific are promoting investments in biotech and biopharma sectors through initiatives like tax rebates and the easing of regulations, which is positively impacting the regional peptide synthesis market.
Europe market is expected to be the fastest-growing market for peptide synthesis, with a share of 19% during the forecast period. The growth of the market in Europe is attributed to the increasing prevalence of sexually transmitted diseases in the region.
The U.S. dominates the market for peptide synthesis globally owing to strong pharmaceutical R&D, intense biotech infrastructure, and a high volume of clinical trials using peptide-based drugs. Key companies such as Thermo Fisher Scientific, CEM Corporation, and AAPPTec have their headquarters in the country, furthering technology and large-scale peptide production.
Germany leads the European peptide synthesis market owing to its sophisticated chemical manufacturing infrastructure and focus on life sciences innovation. Peptide production and research facilities are managed by companies such as Merck KGaA and Bachem, complemented by robust academic–industry partnership in biotechnology.
Switzerland is a central hub for peptide synthesis due to its concentration of specialized peptidyl manufacturers like Bachem and CordenPharma. The nation excels in high-purity GMP peptide synthesis and custom synthesis options to suit global pharmaceutical firms with a strong focus on oncology and metabolic disorder uses.
India is a rising force in peptide synthesis, with increasing export demand and competitive pricing. Indian companies provide custom synthesis, research-grade peptides, and manufacturing services at scale. Support from the government for drug innovation and broader CDMO capabilities is fueling this expansion.
| Report Coverage | Details | ||
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| Base Year: | 2024 | Market Size in 2025: | USD 519.0 Mn |
| Historical Data for: | 2020 To 2024 | Forecast Period: | 2025 To 2032 |
| Forecast Period 2025 to 2032 CAGR: | 7.6% | 2032 Value Projection: | USD 866.7 Mn |
| Geographies covered: |
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| Companies covered: |
GenScript Biotech Corporation, Merck KGaA, ThermoFisher Scientific Inc., Syngene, Lonza, Novo Nordisk A/S, Bachem Holding AG, Gyros Protein Technologies, Creative Diagnostics, CEM Corporation, PuroSynth, AAPPTec, Biotage AB, AnaSpec, ABclonal, Inc. and Novelgene Technologies |
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*Definition: Peptide synthesis is the process of chemically creating peptides, which are chains of amino acids linked together by peptide bonds. It involves the step-by-step addition of amino acids in a specific sequence to build a peptide of a defined length with a specific structure. This process is fundamental in biochemistry and molecular biology and has significant applications in both research and therapeutic developments.
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About Author
Vipul Patil is a dynamic management consultant with 6 years of dedicated experience in the pharmaceutical industry. Known for his analytical acumen and strategic insight, Vipul has successfully partnered with pharmaceutical companies to enhance operational efficiency, cross broader expansion, and navigate the complexities of distribution in markets with high revenue potential.
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