세계의 핵산 치료제 CDMO 시장 - 지역 분석 : 화학 합성법, 제품 유형, 질병 유형, 최종 사용자, 지역별 분석, 예측(2025-2035년)
Nucleic Acid Therapeutics CDMO Market - A Global and Regional Analysis: Focus on Chemical Synthesis Method, Product, Disease Type, End User, and Region - Analysis and Forecast, 2025-2035
상품코드:1754873
리서치사:BIS Research
발행일:2025년 06월
페이지 정보:영문
라이선스 & 가격 (부가세 별도)
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한글목차
핵산 치료제 CDMO 시장은 빠르게 성장하고 있으며, 그 배경에는 몇 가지 주요 요인이 있습니다.
첫째, mRNA, DNA, RNA 치료와 같은 핵산 기반 치료에 대한 수요 증가가 신형 코로나바이러스 감염에 대한 mRNA 백신의 성공을 받아 시장 확대의 큰 원동력이 되고 있습니다. 지질 나노입자 전달 시스템과 바이러스 벡터 제조의 혁신을 포함한 생산 공정의 기술 발전은 보다 효율적이고 확장 가능한 생산을 가능하게 하고 있습니다. 생명공학 기업과 CDMO 간의 파트너십과 투자가 증가하면서 생명공학 기업들이 증가하는 수요를 충족하기 위해 생산을 아웃소싱함에 따라 더욱 성장하고 있습니다. 또한, 규제면의 진전이나 승인 프로세스의 신속화도, 핵산 치료 시장 진입을 가속시키는 추풍이 되고 있습니다. 다양한 분야에서의 응용도 진행되어, 특수한 제조 서비스에 대한 수요가 증가하고 있습니다. 팬데믹으로부터 얻은 교훈도, 핵산 의약품의 중요성을 재인식시켜, 시장의 추가 확대를 촉진하고 있습니다.
그러나 핵산 치료제 CDMO 시장에는 여전히 몇 가지 문제가 있습니다. 가장 큰 장벽 중 하나는 핵산 치료의 제조 복잡성입니다. 이를 스케일업하는 것은 쉽지 않습니다. 일관성, 순도, 수율의 확보와 규제에의 적합을 양립시킬 필요가 있어, 제조 공정에는 복수의 난제가 수반됩니다. 하지만 운영비용 증가로 이어집니다. 또한, 이러한 치료제의 대규모 제조에 대응할 수 있는 CDMO의 수는 한정되어 있어 공급망의 병목이나 납기의 지연을 일으키고 있습니다. 허들도 신약의 승인과 상업화를 늦추는 요인이 되고 있습니다.
본 보고서에서는 세계의 핵산 치료제 CDMO 시장을 조사했으며, 주요 동향, 시장 영향요인 분석, 법규제 환경, 임상시험 동향, 시장 규모 추이와 예측, 각종 구분 지역, 주요 국가별 상세 분석, 경쟁 구도, 주요 기업 프로파일 등을 정리했습니다.
목차
주요 요약
제1장 세계의 핵산 치료제 CDMO 시장 개요
업계 전망
시장 개요와 생태계
주요 동향
기회 평가
특허 분석
생산능력
CDMO에 의한 추천 기술
CDMO에 아웃소싱할 때 고려해야 할 요소
규제 프레임워크
현재의 핵산의약품 CDMO의 정세
핵산의약품의 중요한 이용
치료용으로 합성되는 핵산의 유형
시장 역학
시장 기회와 동향
시장 성장 촉진요인
시장 성장 억제요인
제2장 세계의 핵산 치료제 CDMO 시장 분석 : 화학 합성법별
기회 평가
성장 공유 매트릭스
고상 올리고뉴클레오티드 합성(SPOS)
컬럼법
마이크로어레이법
액상 올리고뉴클레오티드 합성(LPOS)
제3장 세계의 핵산 치료제 CDMO 시장 분석 : 제품별
기회 평가
성장 공유 매트릭스
표준 핵산
마이크로스케일 핵산
커스텀 핵산
수식 핵산
프라이머
프로브
기타 핵산
기타 서비스
제4장 세계의 핵산 치료제 CDMO 시장의 분석 : 질환 유형별
기회 평가
성장 공유 매트릭스
유전성 질환
감염증
제5장 세계의 핵산 치료제 CDMO 시장 분석 : 최종 사용자별
기회 평가
성장 공유 매트릭스
제약회사
학술기관
진단 실험실
제6장 세계의 핵산 치료제 CDMO 시장 분석 : 지역별
북미
주요 조사 결과
시장 역학
시장 규모와 예측
유럽
주요 조사 결과
시장 역학
시장 규모와 예측
아시아태평양
주요 조사 결과
시장 역학
시장 규모와 예측
기타 지역
주요 조사 결과
시장 역학
시장 규모와 예측
제7장 세계의 핵산 치료제 CDMO 시장 : 경쟁 벤치마킹과 기업 프로파일
경쟁 구도
기업 프로파일
Agilent Technologies
AGC Biologics
Asymchem, Inc.
BACHEM
Catalent, Inc.
CMIC Holdings CO. Ltd.
Codexis, Inc.
Danaher Corporation
Eurofins Scientific
GeneOne Life Sciences
LGC Science Group Holdings Limited
Maravai Life Sciences Holdings, Inc.
Merck KGaA
ST Pharm
Thermo Fisher Scientific, Inc.
제8장 조사 방법
SHW
영문 목차
영문목차
Global Nucleic Acid Therapeutics CDMO Market Industry Overview
The global nucleic acid therapeutics CDMO market is experiencing rapid growth, driven by several key factors. The rising demand for nucleic acid-based therapies, such as mRNA, DNA, and RNA treatments, is a major contributor, particularly following the success of mRNA vaccines for COVID-19. Technological advancements in production processes, including innovations in lipid nanoparticle delivery systems and viral vector manufacturing, are enabling more efficient, scalable production. Additionally, the increase in partnerships and investments between biotechnology companies and CDMOs has fueled further growth, as biotech firms outsource production to meet the rising demand. Regulatory advancements and the fast-tracking of approvals for therapies have also created a favorable environment for nucleic acid therapeutics. Finally, the ongoing demand for gene therapies and the lessons learned from the pandemic have underscored the importance of nucleic acid-based treatments, ensuring the continued expansion of nucleic acid therapeutics CDMO market.
Several key factors are driving the growth of the nucleic acid therapeutics CDMO market. First, the increasing demand for nucleic acid-based therapies, particularly mRNA, DNA, and RNA treatments, is fueling market expansion. The success of mRNA vaccines during the COVID-19 pandemic has significantly accelerated interest in these therapies, creating a sustained need for production capacity.
Second, technological advancements in manufacturing, such as improvements in lipid nanoparticle delivery systems and viral vector production, have made large-scale production of these complex molecules more efficient and cost-effective. Additionally, the rise in strategic partnerships and investments between biotech firms and CDMOs has further boosted the sector, as companies seek to outsource production to specialized manufacturers. Regulatory advancements, including faster approval processes, have also contributed to the growth, ensuring quicker market access for new nucleic acid-based therapies. Finally, the growing application of gene therapies for a range of genetic disorders has increased the demand for specialized manufacturing services, further propelling the market forward.
Despite the significant opportunities, several challenges persist in the nucleic acid therapeutics CDMO market. One of the primary obstacles is the complexity of manufacturing nucleic acid-based therapies. The production of mRNA, DNA, and RNA therapies requires highly specialized and precise technologies, which can be difficult to scale up. Ensuring consistency, purity, and yield while maintaining regulatory compliance adds additional layers of complexity. Moreover, the production process is often resource-intensive, requiring advanced facilities, specialized equipment, and a skilled workforce, which can increase operational costs. Another challenge is the limited number of CDMOs with the necessary capabilities and infrastructure to handle the large-scale production of these therapies. This leads to supply chain bottlenecks and delays, particularly as the demand for nucleic acid therapeutics continues to grow. Additionally, regulatory hurdles, including the need for stringent quality control and compliance with international standards, can slow down the approval and commercialization process. These challenges underscore the need for continued innovation, investment, and collaboration to overcome barriers and fully capitalize on the opportunities in the nucleic acid therapeutics CDMO market.
Market Lifecycle Stage of Nucleic Acid Therapeutics CDMO
The global nucleic acid therapeutics CDMO market is currently in a phase of rapid expansion and maturation. As the demand for nucleic acid-based therapies, such as mRNA and gene therapies, continues to grow, CDMOs are scaling up production capabilities to meet the increasing needs of biotech and pharmaceutical companies. This phase is characterized by significant technological advancements, investment influx, and the establishment of strategic partnerships between CDMOs and biopharma companies. Many CDMOs are upgrading their facilities to include advanced capabilities in areas such as lipid nanoparticle formulation and viral vector production, which are critical for the success of nucleic acid-based therapeutics.
The market is also witnessing an accelerated shift toward commercial-scale manufacturing as clinical trials for nucleic acid therapies move toward commercialization. Regulatory processes have become more streamlined, especially in response to the COVID-19 pandemic, which has allowed for faster approval timelines and broader market adoption. However, as the market matures, challenges around scalability, cost-efficiency, and maintaining high-quality standards continue to persist, making it crucial for CDMOs to continually invest in innovation and operational optimization.
Impact for Nucleic Acid Therapeutics CDMO
The nucleic acid therapeutics CDMO market is at the forefront of a transformative shift in biopharmaceutical manufacturing, driven by the accelerating adoption of RNA-based and gene therapies. These therapies, including mRNA, DNA, and RNA-based treatments, are revolutionizing the way diseases, particularly genetic disorders, cancers, and viral infections, are treated. The ability to produce and scale these therapies efficiently is heavily reliant on the expertise of Contract Development and Manufacturing Organizations (CDMOs) that specialize in complex biopharmaceutical manufacturing processes.
Key technological advancements in the nucleic acid therapeutics CDMO market include:
Lipid Nanoparticle (LNP) Technology: The use of LNPs has become crucial for the delivery of mRNA and RNA therapies. CDMOs with expertise in LNP formulation are well-positioned to support the growing demand for RNA-based vaccines and gene therapies. These innovations are enhancing the efficiency of nucleic acid delivery systems and improving therapeutic outcomes.
Viral Vector Production: The manufacturing of viral vectors, which are essential for gene therapies, has seen significant advancements. CDMOs that specialize in viral vector production are increasingly in demand, as gene therapies using viral vectors are being developed for a wide range of diseases.
Automated Manufacturing Systems: Automation and continuous bioprocessing are revolutionizing nucleic acid therapeutics production by enabling scalable, cost-effective, and efficient manufacturing. Automation minimizes human error and ensures consistency and purity in the production of complex molecules like mRNA.
CRISPR and Gene Editing Technologies: CRISPR gene editing has expanded the scope of nucleic acid-based therapies. CDMOs are leveraging CRISPR technology to support the development and manufacturing of gene-editing therapies that can potentially cure genetic disorders at their root cause.
Regulatory Evolution and Approval Processes in Nucleic Acid Therapeutics CDMO Market:
The regulatory environment has been adapting to meet the needs of the fast-evolving nucleic acid therapeutics landscape. Authorities like the U.S. FDA and European Medicines Agency (EMA) have fast-tracked approval processes for RNA-based therapies, particularly in response to the global demand for COVID-19 vaccines.
Regulatory agencies are also increasingly providing clearer guidelines for the manufacturing and testing of gene therapies, which has encouraged more biotech firms to enter the nucleic acid therapeutics space. This shift has created a favorable environment for CDMOs, who play a key role in ensuring that therapies meet stringent regulatory standards for clinical trials and commercial production.
Impact of mRNA Vaccines:
The success of mRNA vaccines during the COVID-19 pandemic has had a profound impact on the nucleic acid therapeutics CDMO market. It has proven the efficacy and speed at which nucleic acid-based therapies can be developed and deployed, which has greatly accelerated the adoption of mRNA technologies for other diseases, including cancer and genetic disorders. This shift has led to an increased reliance on CDMOs to manufacture mRNA vaccines and other nucleic acid therapies at an unprecedented scale.
As vaccine development pipelines expand, particularly in oncology and infectious diseases, the demand for CDMOs with mRNA capabilities is expected to grow. CDMOs are increasingly investing in the necessary facilities, equipment, and expertise to handle the complexity and scale of mRNA production.
Gene Therapy Expansion:
Gene therapies, particularly those using viral vectors and RNA technologies, are becoming more prevalent for treating genetic diseases. Gene therapies offer potential cures for conditions previously thought to be untreatable, such as sickle cell anemia, muscular dystrophy, and hemophilia.
The increased development of these therapies is boosting the demand for CDMOs with the expertise and infrastructure to support the complex and often personalized manufacturing processes associated with gene therapies. This includes the production of plasmids, viral vectors, and other gene-editing technologies such as CRISPR. As gene therapies move closer to commercialization, CDMOs with specialized manufacturing capabilities are poised to play a critical role in bringing these therapies to market at scale.
Global Demand and Scalability:
With the rising global demand for nucleic acid therapeutics, there is a growing need for CDMOs to offer large-scale manufacturing capabilities. The scalability of production is critical, as these therapies often need to be produced in large volumes to meet worldwide demand, particularly for vaccines and gene therapies.
CDMOs are expanding their facilities and increasing production capacity to meet this demand. The ability to scale efficiently, while maintaining high-quality standards and regulatory compliance, is a key competitive advantage. The demand for commercial-grade mRNA vaccines and other therapies is projected to remain strong, creating a long-term opportunity for CDMOs to capitalize on this growth.
Market Segmentation for Nucleic Acid Therapeutics CDMO Market:
Segmentation 1: by Product Type
Standard Nucleic Acid
Micro-Scale Nucleic Acid
Custom Nucleic Acid
Modified Nucleic Acid
Primers
Probes
Other Nucleic Acid
Other Services
The global nucleic acid therapeutics CDMO market (by product type) is expected to be dominated by the standard nucleic acid segment.
Segmentation 2: by Disease Type
Genetic Disease
Infectious Disease
The global nucleic acid therapeutics CDMO market (by disease type) is expected to be dominated by genetic disease.
Segmentation 3: By Chemical Synthesis Method
Solid-Phase Oligonucleotide Synthesis
Liquid-Phase Oligonucleotide Synthesis
The global nucleic acid therapeutics CDMO market (by chemical synthesis method) is expected to be dominated by solid-phase oligonucleotide synthesis.
Segmentation 4: By End User
Pharmaceutical Companies
Academic Research Institute
Diagnostic Laboratories
The global nucleic acid therapeutics CDMO market (by end-user) is expected to be dominated by pharmaceutical companies.
Segmentation 5: by Region
North America: U.S., and Canada
Europe: Germany, U.K., France, Italy, Spain, and Rest-of-Europe
Asia-Pacific: China, Japan, South Korea, India, Australia, and Rest-of-Asia-Pacific
Rest-of-the-World
The global nucleic acid therapeutics CDMO market (by region) is dominated by the North America region.
Recent Developments in the Global Nucleic Acid Therapeutics CDMO Market
In January 2023, Agilent Technologies, Inc. invested $725 million to increase its manufacturing capacity for therapeutic nucleic acids.
In March 2022, IMM, a partner of VGXI, has recently announced that it received a $12 million grant from the National Institutes of Health (NIH) to support the Phase 1 clinical trial of a DNA vaccine aimed at preventing Alzheimer's disease. The vaccine will be manufactured using VGXI's expertise in contract manufacturing of DNA plasmids for human clinical trials, produced in accordance with GMP standards.
In April 2022, BACHEM partnered with Eli Lilly and Company to develop and manufacture active pharmaceutical ingredients based on oligonucleotides, a rising new class of complex molecules.
In September 2021, AGC Biologics expanded the company's Heidelberg facility to increase manufacturing capacities for plasmid-DNA (pDNA) and messenger RNA (mRNA) projects.
In August 2022, Codexis and Molecular Assemblies announced the execution of a commercial license and enzyme supply agreement for an optimized TdT enzyme for enzymatic DNA synthesis.
In June 2020, OliX Pharmaceuticals, Inc. partnered with LGC Biosearch Technologies Inc. to scale up the production of OliX's OLX301D therapeutic candidate.
Demand - Drivers and Limitations for Nucleic Acid Therapeutics CDMO
Market Demand Drivers for Nucleic Acid Therapeutics CDMO:
Growing demand for nucleic acid therapeutics applications to treat chronic and genetic diseases.
Increasing FDA or European Medicines Agency (EMA) approvals of nucleic acid Therapeutics
Advancements in manufacturing units for producing nucleic acid by CDMO.
Market Restraints for Nucleic Acid Therapeutics CDMO:
Substantial variation in nucleic acid leads to complications in therapeutic classification.
Lack of expertise in developing nucleic acid therapeutics
Market Opportunities for Nucleic Acid Therapeutics CDMO:
Continued research and development activities for manufacturing innovative nucleic acid therapeutics forcing pharmaceutical companies to expand their businesses.
Pharmaceutical Firms Becoming More Outsourcing-Oriented
How can nucleic acid therapeutics CDMO market report add value to an organization?
Workflow/Innovation Strategy: The nucleic acid therapeutics CDMO market (by product type) has been segmented into standard nucleic acid, micro-scale nucleic acid, custom nucleic acid, modified nucleic acid, primers, probes, other nucleic acid, and other services. Moreover, the study provides the reader with a detailed understanding of the different applications of nucleic acid therapeutics CDMO in raw material preparation, upstream processing, downstream processing, and packaging.
Growth/Marketing Strategy: Cell and gene therapy biomanufacturing is being used for raw material preparation, upstream processing, downstream processing, and packaging. Various companies are providing products and services to aid in the manufacturing of various cell and gene therapies, which is also the key strategy for market players to excel in the current nucleic acid therapeutics CDMO market.
Competitive Strategy: Key players in the global nucleic acid therapeutics CDMO market have been analyzed and profiled in the study, including manufacturers involved in new product launches, acquisitions, expansions, and strategic collaborations. Moreover, a detailed competitive benchmarking of the players operating in the global nucleic acid therapeutics CDMO market has been done to help the reader understand how players stack against each other, presenting a clear market landscape. Additionally, comprehensive competitive strategies such as partnerships, agreements, and collaborations will aid the reader in understanding the untapped revenue pockets in the nucleic acid therapeutics CDMO market.
Methodology
Key Considerations and Assumptions in Nucleic Acid Therapeutics CDMO Market Engineering and Validation
The base year considered for the calculation of the nucleic acid therapeutics CDMO market size is 2024. The historical year analysis has been done from FY2021 to FY2023, and the market size has been estimated for FY2024 and projected for the period 2025-2035.
The regional distribution of the market revenue has been estimated to be the same as the company's net revenue distribution. All the numbers have been adjusted off to two digits after decimal for report presentation reasons. However, the real figures have been utilized for compound annual growth rate (CAGR) estimation. The CAGR has been calculated for the forecast period 2025-2035.
Nucleic acid therapeutics CDMO market has been mapped based on different types of products available in the market for various applications. All key companies having a significant number of offerings for the global nucleic acid therapeutics CDMO market have been considered and profiled in the report.
The primary respondent's verification has been considered to finalize the estimated market for the global nucleic acid therapeutics CDMO market.
The latest annual reports of each market player have been taken into consideration for nucleic acid therapeutics CDMO market revenue calculation.
Market strategies and developments of key players have been considered for the calculation of the sub-segment split.
The base currency considered for the nucleic acid therapeutics CDMO market analysis is US$. Currencies other than the US$ have been converted to the US$ for all statistical calculations, considering the average conversion rate for that particular year. The currency conversion rate has been taken from the historical exchange rate of the Oanda website.
Primary Research
The key data points taken from the primary sources include:
Validation and triangulation of all the numbers and graphs
Validation of the report's segmentation and key qualitative findings
Understanding of the numbers of the various markets for market type
Percentage split of individual markets for regional analysis
Secondary Research
Open Sources
Central Drugs Standard Control Organization (CDSCO), Comision Federal para la Proteccion contra Riesgos Sanitarios (COFEPRIS), European Medicines Agency (EMA), Institute for Health Metrics and Evaluation (IHME), Medicines and Healthcare Products Regulatory Agency (MHRA), National Organization for Rare Disorders (NORD), Pharmaceuticals and Medical Devices Agency (PMDA), World Health Organization (WHO), and World Intellectual Property Organization (WIPO)
Annual reports, SEC filings, and investor presentations of the leading market players
Company websites and detailed study of their portfolio
Gold standard magazines, journals, whitepapers, press releases, and news articles
Databases
The key data points taken from the secondary sources include:
Segmentations, split-ups, and percentage shares
Data for market value
Key industry trends of the top players in the market
Qualitative insights into various aspects of the market, key trends, and emerging areas of innovation
Quantitative data for mathematical and statistical calculations
Key Market Players and Competition Synopsis for Nucleic Acid Therapeutics CDMO
The nucleic acid therapeutics CDMO (Contract Development and Manufacturing Organization) market is highly competitive, with several prominent players that specialize in the development and manufacturing of nucleic acid-based therapies, including mRNA, DNA, RNA, and gene therapies. These companies offer specialized services ranging from process development to large-scale commercial manufacturing. The competitive landscape is shaped by factors such as technological innovation, production capacity, regulatory compliance, and strategic partnerships with biotech firms and pharmaceutical companies.
Some of the prominent companies in nucleic acid therapeutics CDMO market are:
Danaher Corporation
Thermo Fisher Scientific Inc.
Merck KGaA
Agilent Technologies, Inc
ST Pharm
GeneOne Life Science
LGC Science Group Holdings Limited
BACHEM
Eurofins Scientific
Kaneka Corporation
CMIC HOLDINGS Co., Ltd
Nippon Shkubai Co., Ltd
AGC Biologics
Codexis, Inc.
Asymchem Inc.
Maravai LifeSciences Holdings, Inc.
Table of Contents
Executive Summary
Scope of Study
Research Methodology
1. Global Nucleic Acid Therapeutics CDMO Market Overview
1.1 Industry Outlook
1.1.1 Introduction
1.1.2 Market Overview and Ecosystem
1.1.3 Key Trends
1.1.4 Opportunity Assessment
1.1.5 Patent Analysis
1.1.6 Production Capability
1.1.7 Preferred Techniques by CDMO
1.1.7.1 Preferred Techniques by CDMOs for Nucleic Acid Impurity Analysis
1.1.7.2 Preferred Techniques by CDMOs for Nucleic Acid Structural Analysis
1.1.7.3 Preferred Techniques by CDMOs for Nucleic Acid Purification
1.1.8 Factors Considered While Outsourcing to CDMO
1.1.9 Regulatory Framework
1.1.10 Current Nucleic Acid Therapeutics CDMO Landscape
1.1.11 Significant Usage of Nucleic Acid Therapeutics
1.1.12 Types of Nucleic Acid Synthesized for Therapeutics
1.1.12.1 Anti-sense Oligonucleotides and DNA Aptamers
1.1.12.2 RNA Interference (RNAi) and Short Interfering RNAs (siRNAs)
1.1.12.3 MicrRNAs (miRNAs)
1.1.12.4 Ribozymes
1.1.12.5 Circular RNA
1.2 Market Dynamics
1.2.1 Market Opportunities and Trends
1.2.2 Market Drivers
1.2.2.1 Impact Analysis
1.2.3 Market Restraints
1.2.3.1 Impact Analysis
2. Global Nucleic Acid Therapeutics CDMO Market Analysis (by Chemical Synthesis Method), $Million, 2023-2035
