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Rising Investment In Gene Therapy Research Driving The Growth Of The Market Due To Its Potential For Long-Term And Curative Treatments: Powering Innovation and Expansion in the Global Viral Vector Contract Development And Manufacturing Organization (CDMO)

11-12-2025 05:24 AM CET | Health & Medicine

Press release from: The Business Research Company

Viral Vector Contract Development And Manufacturing Organization CDMO

Viral Vector Contract Development And Manufacturing Organization CDMO

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What Is the Expected CAGR for the Viral Vector Contract Development And Manufacturing Organization (CDMO) Market Through 2025?
The market for contract development and manufacturing organizations specializing in viral vectors has seen swift expansion lately, projected to increase its value from $1.27 billion at the start of 2024 to $1.47 billion for 2025, demonstrating a compound annual growth rate (CAGR) of 15.8%; this upward trajectory observed historically stems from several factors, including the mounting volume of clinical trials involving gene and cell therapies, heightened spending across the healthcare sector, the validation of viral-vector treatments through early regulatory clearances, increased capital flowing into dedicated manufacturing infrastructure, and the dependence on essential plasmid DNA sourcing.

What's the Projected Size of the Global Viral Vector Contract Development And Manufacturing Organization (CDMO) Market by 2029?
Anticipation surrounds the viral vector contract development and manufacturing organization sector, projecting substantial expansion ahead; this market is forecasted to reach a valuation of 2.61 billion dollars by 2029, driven by a compound annual growth rate (CAGR) of 15.4%. This upward trajectory during the projected period is sustained by several key factors: the successful launch of additional gene therapies addressing both prevalent and uncommon ailments, the swift scaling up of outsourced capabilities coupled with considerable CDMO capital expenditure, convergence in regulatory frameworks, the increasing need for manufacturing solutions that are either personalized, on-demand, or autologous, and the escalating prevalence of long-term health conditions. Key movements shaping this forecast span several domains, including intensified mergers and acquisitions alongside upstream and downstream integration among major CDMOs and pharmaceutical entities, localized expansion of production footprints, an ongoing imperative to lower expenses through refined process development and achieving economies of scale, expansion into adjacent service areas such as plasmid DNA manufacturing, non-viral delivery methods, and final filling and finishing procedures, alongside the integration of digital technologies and artificial intelligence for enhanced process oversight and quality assurance.

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Top Growth Drivers in the Viral Vector Contract Development And Manufacturing Organization (CDMO) Industry: What's Accelerating the Market?
Anticipated expansion in the realm of gene therapy studies is set to boost trajectories within the viral vector contract development and manufacturing organization (CDMO) sector in the foreseeable future. This line of inquiry, gene therapy, centers on devising pathways to modify or govern genes situated within human cells, aiming to rectify inherited conditions or address diverse ailments. Substantial capital allocation toward gene therapy exploration is on the upswing, spurred by its promise of enduring or definitive remedies for genetic illnesses that were previously beyond therapeutic reach, thus generating considerable enthusiasm among those developing healthcare solutions and financial backers alike. Viral vector CDMOs act as critical enablers for these gene therapy endeavors, providing specialized proficiency and cutting-edge manufacturing environments necessary for producing premium viral vectors, essential components for the secure and efficacious transport of therapeutic genes. Illustratively, the UK's Office for Life Sciences announced in July 2025 a significant financial pledge of up to $800 million (equivalent to £600 million) toward establishing one of the globe's most sophisticated, protected, and AI-ready health data infrastructures, synthesizing population-level genomic, diagnostic, and clinical data to reconfigure NHS and general healthcare information into a nexus attracting international research studies and AI capital; consequently, this escalating commitment to gene therapy research directly fuels the expansion of the viral vector CDMO market.

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What Trends Will Shape the Viral Vector Contract Development And Manufacturing Organization (CDMO) Market Through 2029 and Beyond?
Key players within the viral vector contract development and manufacturing organization (CDMO) sector are prioritizing the creation of sophisticated offerings, specifically AAV manufacturing techniques, to facilitate production that is both scalable and uniform. These AAV manufacturing solutions comprise specialized methodologies and apparatuses engineered for the effective creation of secure and potent adeno-associated virus vectors crucial for gene therapies. Illustratively, in August of 2025, ProBio, a CDMO headquartered in the United States, initiated current Good Manufacturing Practice (cGMP) Adeno-Associated Virus (AAV) production services operating out of their expansive, modern 128,000 square foot site situated in Hopewell, New Jersey. This strategic growth initiative aims to satisfy the rising need for superior viral vector output, simultaneously showcasing ProBio's commitment to advancing novel gene therapy development. The Hopewell complex has been specifically designed to deliver comprehensive AAV manufacturing support, adhering strictly to international quality and regulatory benchmarks. Furthermore, ProBio's service portfolio now encompasses entirely integrated functions, including the production of GMP plasmid DNA, the manufacturing of AAV vectors, and the final formulation of the drug product complete with aseptic fill/finish procedures, all centralized within one US-based location, thereby streamlining communication, minimizing transitions between stages, and accelerating schedules throughout the entire drug development continuum.

What Are the Main Segments in the Viral Vector Contract Development And Manufacturing Organization (CDMO) Market?
The viral vector contract development and manufacturing organization (cdmo)market covered in this report is segmented -

1) By Service Type: Process Development, Manufacturing, Analytical Testing, Fill-Finish, Other Service Types
2) By Vector Type: Adenoviral Vectors, Lentiviral Vectors, Adeno-Associated Viral Vectors, Retroviral Vectors, Other Vector Types
3) By Workflow: Upstream Manufacturing, Downstream Manufacturing
4) By Application: Gene Therapy, Vaccines, Cell Therapy, Other Applications
5) By End-User: Pharmaceutical And Biotechnology Companies, Academic And Research Institutes, Other End-Users

Subsegments:
1) By Process Development: Upstream Process Development, Downstream Process Development, Analytical Development, Process Characterization
2) By Manufacturing: Clinical Manufacturing, Commercial Manufacturing, cGMP Manufacturing, Cell Bank Production, Fill-Finish Services
3) By Analytical Testing: Release Testing, Stability Testing, Bioassays, Characterization Studies, Regulatory Compliance Testing
4) By Fill-Finish: Aseptic Filling, Lyophilization, Final Packaging, Cold Chain Management, Labeling And Serialization
5) By Other Service Types: Regulatory Support, Supply Chain Management, Technology Transfer, Clinical Trial Support, Cold Chain Logistics

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Which Top Companies are Driving Growth in the Viral Vector Contract Development And Manufacturing Organization (CDMO) Market?
Major companies operating in the viral vector contract development and manufacturing organization (CDMO) market are Thermo Fisher Scientific Inc., Merck KGaA, Lonza Group AG, WuXi AppTec, Samsung Biologics Co. Ltd., FUJIFILM Biotechnologies, Oxford Biomedica Plc, Hillgene, Takara Bio Inc., SkyPharma Production SAS, GeneScript ProBio, Obio Technology Corp. Ltd., VectorBuilder, Charles River Laboratories Pvt. Ltd., Creative Biogene, Esco Aster Pte. Ltd., Genesail Biotech Co. Ltd., CEVEC Pharmaceuticals, Cell and Gene Therapy Catapult, CoJourney, and Applied Biological Laboratories Inc.

Which Regions Will Dominate the Viral Vector Contract Development And Manufacturing Organization (CDMO) Market Through 2029?
North America was the largest region in the viral vector contract development and manufacturing organization (CDMO) market in 2024. Asia-Pacific is expected to be the fastest-growing region in the forecast period. The regions covered in the viral vector contract development and manufacturing organization (CDMO) market report are Asia-Pacific, Western Europe, Eastern Europe, North America, South America, Middle East, Africa.

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