Global Gene Therapy Starting Materials Market Size study, by Product (Viral Vectors, Plasmid DNA, Cell Lines), Development Stage, Application, End Use and Regional Forecasts 2022-2032

Global Gene Therapy Starting Materials Market is valued approximately at USD 1.59 billion in 2023 and is anticipated to grow with an impressive growth rate of more than 19.24% over the forecast period 2024-2032. Gene therapy, a paradigm-shifting advancement in the realm of precision medicine, hinges on the foundation of robust and high-quality starting materials such as viral vectors, plasmid DNA, and specialized cell lines. These materials are integral to the development and manufacturing of gene therapy products, which aim to treat, prevent, or potentially cure genetic disorders by introducing, altering, or silencing genes within a patient’s cells. With an expanding array of gene-based therapies advancing from the lab bench to clinical pipelines and beyond, the demand for highly specialized raw materials has surged exponentially. The complexity of producing safe and efficacious gene therapies has spurred a wave of innovation in the production and standardization of these inputs, ushering in a new era for upstream bioprocessing capabilities.

The market is witnessing an accelerated momentum owing to a confluence of pivotal factors. The rising incidence of genetic disorders and rare diseases, combined with the surging number of gene therapy clinical trials, continues to amplify the urgency for streamlined and scalable manufacturing solutions. Governments and private entities alike are funneling unprecedented investments into gene therapy infrastructure. For example, public-private partnerships and regulatory incentives across the U.S. and EU are expediting the development and commercialization of advanced therapies, including those based on adeno-associated virus (AAV) and lentiviral vectors. Moreover, the growing adoption of CRISPR and other gene editing platforms has substantially increased the complexity and volume of genetic payloads, thus driving demand for bespoke plasmids and tailor-engineered cell lines. Despite these tailwinds, challenges such as regulatory variability, production scalability, and high costs associated with GMP-grade material production remain pressing concerns, restraining the market’s full potential.

The surge in biopharmaceutical R&D activities globally is fueling the requirement for optimized gene therapy starting materials. Emerging biotech firms and research institutes are increasingly outsourcing the production of vectors and plasmids to specialized CDMOs to reduce time-to-market. Furthermore, integration of AI-powered analytics and automation in upstream bioprocess development is poised to enhance productivity and consistency in raw material manufacturing. Additionally, companies are working on establishing platform-based production strategies that allow faster and cost-effective scale-up of clinical-grade vectors. This focus on standardization is not only ensuring product reproducibility but is also helping in addressing the batch-to-batch variability—a long-standing hurdle in gene therapy production.

Several regional markets are displaying dynamic patterns of growth. North America currently holds the lion’s share of the global market, bolstered by the presence of leading biotechnology firms, favorable reimbursement structures, and advanced regulatory frameworks. The United States, in particular, has established itself as a nucleus for gene therapy innovation, with a growing number of FDA-approved therapies and an increasing volume of IND filings. Europe follows closely, driven by a robust academic research base and initiatives such as the EU’s Horizon Europe program, which supports gene therapy-focused projects. Meanwhile, the Asia Pacific region is emerging as the fastest-growing market, catalyzed by rising investments in genomic medicine, expanding biomanufacturing capabilities in countries like China, India, and South Korea, and a rapidly evolving regulatory environment conducive to gene therapy development.

Major market player included in this report are:
• Thermo Fisher Scientific, Inc.
• Charles River Laboratories International, Inc.
• Catalent, Inc.
• Lonza Group Ltd.
• Oxford Biomedica plc
• Wuxi AppTec Co., Ltd.
• FUJIFILM Diosynth Biotechnologies
• Takara Bio Inc.
• Aldevron LLC
• MilliporeSigma (Merck KGaA)
• Bio-Techne Corporation
• Cobra Biologics (Charles River)
• Sarepta Therapeutics, Inc.
• GenScript Biotech Corporation
• AGC Biologics

The detailed segments and sub-segment of the market are explained below:

By Product
• Viral Vectors
• Plasmid DNA
• Cell Lines

By Development Stage
• Preclinical
• Clinical
• Commercial

By Application
• Gene Editing
• Cell Therapy
• Genetic Disorders
• Oncology
• Others

By End Use
• Biotechnology and Pharmaceutical Companies
• Academic and Research Institutes
• CDMOs (Contract Development and Manufacturing Organizations)
• Hospitals and Clinics

By Region:

North America
• U.S.
• Canada

Europe
• UK
• Germany
• France
• Spain
• Italy
• Rest of Europe

Asia Pacific
• China
• India
• Japan
• Australia
• South Korea
• Rest of Asia Pacific

Latin America
• Brazil
• Mexico

Middle East & Africa
• Saudi Arabia
• South Africa
• Rest of Middle East & Africa

Years considered for the study are as follows:

Historical year – 2022

Base year – 2023

Forecast period – 2024 to 2032

Key Takeaways:
• Market Estimates & Forecast for 10 years from 2022 to 2032.
• Annualized revenues and regional level analysis for each market segment.
• Detailed analysis of geographical landscape with Country level analysis of major regions.
• Competitive landscape with information on major players in the market.
• Analysis of key business strategies and recommendations on future market approach.
• Analysis of competitive structure of the market.
• Demand side and supply side analysis of the market.

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