Viral Vector and Plasmid DNA Manufacturing Market – Global Industry Size, Share, Trends, Opportunity, and Forecast, Segmented by Product Type (Plasmid DNA, Viral Vector, and Non-viral Vector), Application (Cancer, Genetic Disorder, Infectious Disease, and Other Applications), By Region, and Competition 2018-2028
Published Date: November - 2024 | Publisher: MIR | No of Pages: 320 | Industry: Healthcare | Format: Report available in PDF / Excel Format
View Details Buy Now 2890 Download Sample Ask for Discount Request CustomizationViral Vector and Plasmid DNA Manufacturing Market – Global Industry Size, Share, Trends, Opportunity, and Forecast, Segmented by Product Type (Plasmid DNA, Viral Vector, and Non-viral Vector), Application (Cancer, Genetic Disorder, Infectious Disease, and Other Applications), By Region, and Competition 2018-2028
| Forecast Period | 2024-2028 |
| Market Size (2022) | 5.49 billion |
| CAGR (2023-2028) | 10.89% |
| Fastest Growing Segment | Cancer |
| Largest Market | North America |
Market Overview
Global Viral Vector and Plasmid DNA Manufacturing Market has valued at USD 5.49 billion in 2022 and is anticipated to witness an impressive growth in the forecast period with a CAGR of 10.89% through 2028.
Ongoing advancements in biotechnology, including gene editing techniques like CRISPR-Cas9, have expanded the possibilities for gene therapy. This has driven the need for efficient and safe delivery systems, which viral vectors and plasmid DNA provide.
Key Market Drivers
Advancements in Biotechnology
Technologies like CRISPR-Cas9 have revolutionized genetic engineering. They allow precise and efficient modification of genes in various organisms, holding tremendous potential for treating genetic diseases, creating genetically modified organisms (GMOs), and advancing basic research. Advances in genomics have made it possible to sequence entire genomes quickly and cost-effectively. This has paved the way for personalized medicine, where treatments are tailored to an individual's genetic makeup, increasing treatment efficacy, and reducing side effects. The biopharmaceutical industry has grown significantly, producing complex drugs like monoclonal antibodies, vaccines, and gene therapies. Biomanufacturing techniques have improved, leading to more efficient and cost-effective production of these drugs. Synthetic biology involves designing and constructing biological parts, devices, and systems to perform specific functions. This field has led to the creation of synthetic organisms, biosensors, and biofuels. Stem cell research has advanced significantly, leading to the development of stem cell therapies for various diseases and injuries. These therapies have the potential to regenerate damaged tissues and organs. Advances in bioinformatics have enabled the efficient storage, analysis, and interpretation of vast amounts of biological data. This is crucial for genomics, drug discovery, and understanding complex biological processes. Biotechnology is being used to address environmental challenges, such as pollution remediation, waste management, and the development of biofuels and bioplastics.
Genetically modified crops (GMOs) have been developed to improve crop yield, resistance to pests and diseases, and nutritional content. This technology has the potential to enhance food security and sustainability. Biotechnology has led to the development of novel vaccines and immunotherapies for infectious diseases and cancer. These treatments harness the body's immune system to combat diseases. The study of the human microbiome has revealed the crucial role of microorganisms in human health. Advances in microbiome research have implications for understanding and treating various diseases. The integration of nanotechnology with biotechnology has led to the development of nanoparticles and nanoscale tools for drug delivery, imaging, and diagnostics. 3D bioprinting technology allows the fabrication of complex tissues and organs using living cells. This has potential applications in regenerative medicine and tissue engineering. Biotechnology is used to develop biosensors and bioremediation techniques for monitoring and cleaning up environmental pollutants. AI and machine learning are increasingly used to analyze biological data, model biological systems, and assist in drug discovery and development. This factor will help in the development of
Increasing Investment in Gene Therapy
Gene therapy involves the introduction of therapeutic genes or genetic material into a patient's cells to treat or prevent disease. Viral vectors and plasmid DNA serve as essential tools for delivering these therapeutic genes into target cells. Viral vectors, such as adeno-associated viruses (AAVs) or lentiviruses, are used for in vivo gene therapy, while plasmid DNA is often employed in ex vivo gene therapy. The development of gene therapies starts with extensive research and preclinical studies. This research phase often involves testing different viral vectors and plasmid DNA constructs to optimize delivery and expression of therapeutic genes. Investment in research drives the demand for these materials. Gene therapies must go through rigorous clinical trials to demonstrate safety and efficacy before they can be approved for widespread use. These trials require substantial quantities of viral vectors and plasmid DNA, especially as they progress to larger patient populations. Once a gene therapy is proven effective in clinical trials, it enters the commercialization phase. This involves scaling up production to meet market demand. Viral vectors and plasmid DNA manufacturers play a critical role in providing the necessary materials for large-scale production.
Gene therapy has a wide range of applications beyond rare genetic diseases, including cancer, neurodegenerative disorders, and cardiovascular diseases. The versatility of viral vectors and plasmid DNA makes them suitable for various therapeutic areas, further increasing demand. Regulatory agencies like the FDA in the United States have launched expedited pathways and designations for promising gene therapies. These pathways encourage investment in gene therapy development and manufacturing. Success stories in gene therapy, such as the approval of Luxturna and Zolgensma, have bolstered investor confidence in the field. Increased funding from both venture capital and pharmaceutical companies fuels the development and manufacturing of viral vectors and plasmid DNA. The demand for gene therapies is not limited to a single region. It is a global market, and as more countries recognize the potential of gene therapy, there is a growing need for a reliable supply of viral vectors and plasmid DNA worldwide. Ongoing advancements in bioprocessing and manufacturing techniques for viral vectors and plasmid DNA are making production more efficient and cost-effective, aligning with the needs of a growing market. Gene therapy offers the potential for transformative treatments, which attracts investment and support from patients, advocacy groups, and healthcare systems. This factor will pace up the demand of
Technological Advancements
Single-use bioreactors have gained popularity in biopharmaceutical manufacturing, including viral vector and plasmid DNA production. These disposable systems offer flexibility, reduce the risk of contamination, and decrease setup times compared to traditional stainless-steel bioreactors. Advances in cell culture media and bioprocess optimization have led to higher cell densities and productivity. This results in increased yields of viral vectors and plasmid DNA from bioreactors, reducing production costs. The development of stable and high-yielding cell lines for viral vector and plasmid DNA production has led to more efficient and consistent manufacturing processes. Modified cell lines optimized for specific applications can increase productivity. New chromatography and purification techniques have been developed to enhance the purity and yield of viral vectors and plasmid DNA. Improved resin materials, column designs, and purification strategies contribute to higher product quality. Closed and automated systems minimize the risk of contamination, reduce operator intervention, and increase the reproducibility of manufacturing processes. These systems are particularly important in the production of viral vectors and plasmid DNA for clinical applications. Advances in analytical techniques and quality control methods enable real-time monitoring and characterization of viral vector and plasmid DNA products. This ensures product consistency and helps meet regulatory requirements.
Process Analytical Technology (PAT) tools, including sensors and data analytics, are integrated into manufacturing processes to provide real-time data and enable process control and optimization. This enhances product quality and reduces the need for time-consuming offline testing. Scalable manufacturing platforms are crucial to meet the increasing demand for viral vectors and plasmid DNA. Modular and flexible systems allow for easy scale-up from research and development to commercial production. New platforms and technologies for viral vector production, such as baculovirus-insect cell systems and transient transfection using suspension-adapted cell lines, offer alternatives to traditional adherent cell culture methods. Continuous manufacturing approaches are being explored to replace batch processes in viral vector and plasmid DNA production.
Continuous systems offer greater productivity, reduced production time, and smaller facility footprints. Enhanced safety measures, such as containment systems and viral inactivation technologies, have been developed to mitigate the risks associated with handling viral vectors, especially when working with pathogenic viruses. Overall cost reduction strategies, including more efficient use of resources, optimization of raw materials, and improved process yields, contribute to the affordability and accessibility of viral vectors and plasmid DNA products. Manufacturers are increasingly focused on sustainability, exploring eco-friendly materials and processes to reduce the environmental impact of viral vector and plasmid DNA production. This factor will accelerate the demand of
Key Market Challenges
Costs and Pricing Pressures
Viral vector and plasmid DNA manufacturing processes can be complex, involving multiple steps and the use of specialized equipment and materials. These processes can be costly to establish and operate, leading to higher production costs. As gene therapies progress from research and development to commercial production, companies face the challenge of scaling up manufacturing processes. Achieving economies of scale while maintaining product quality is a delicate balance that impacts costs. Meeting stringent regulatory requirements for gene therapy products adds additional costs to manufacturing. Companies must invest in quality control, documentation, and compliance measures, which can be resource intensive. Ensuring the safety and efficacy of viral vectors and plasmid DNA products requires rigorous quality control and assurance processes. These processes can increase production costs, especially when addressing deviations or maintaining consistent quality. Building and maintaining state-of-the-art manufacturing facilities and cleanrooms compliant with Good Manufacturing Practices (GMP) standards is a significant upfront investment that can lead to cost pressures. The cost of raw materials, such as cell culture media, growth factors, and purification reagents, can impact overall manufacturing costs. Supply chain disruptions or fluctuations in raw material prices can increase these costs.
Ethical and Societal Considerations
The ability to modify genes raises concerns about the potential for genetic enhancement and the creation of designer babies. Ethical debates revolve around the boundaries of gene editing and the implications for future generations. Ensuring that patients fully understand the risks and benefits of gene therapy is crucial. Obtaining informed consent from patients and, in some cases, their families or guardians, can be challenging, especially when dealing with vulnerable populations. There are concerns about equitable access to gene therapies. High costs can limit access to these treatments, potentially exacerbating health disparities. Ensuring affordability and accessibility for all patients is an ethical imperative. Gene therapies are relatively new, and their long-term safety and efficacy are not always well-understood.
Ethical considerations include the need for ongoing monitoring and the obligation to report adverse events. Editing the germline (sperm and egg cells) raises significant ethical questions. Permanent genetic changes made to the germline can be passed on to future generations, potentially altering the human gene pool. Obtaining informed consent for germline editing is particularly complex, as the implications extend to descendants who cannot provide consent. Global discussions are ongoing to establish guidelines and regulations for such interventions.
Key Market Trends
Cell and Gene Therapy Ecosystem Development
Collaboration among academic institutions, research organizations, and biopharmaceutical companies is crucial for advancing cell and gene therapy technologies. These partnerships enable the exchange of knowledge, expertise, and resources, accelerating the development of innovative therapies. Many countries have established specialized research centers and institutes dedicated to cell and gene therapy research. These centers serve as hubs for cutting-edge research and provide a nurturing environment for scientists and innovators. Biotechnology clusters or hubs, often located in regions with a strong biotech presence, foster innovation, collaboration, and investment in cell and gene therapy. Examples include the Boston-Cambridge area in the United States and the Golden Triangle in the United Kingdom. Governments and private entities are providing funding and grants to support cell and gene therapy research and development.
These initiatives help attract top talent and stimulate innovation in the field. Regulatory agencies are actively engaged in shaping policies and pathways for cell and gene therapies. They provide guidance, expedited review processes, and incentives to facilitate product development and approvals. Investments in manufacturing facilities and infrastructure that meet Good Manufacturing Practices (GMP) standards are essential. This includes the construction of specialized cell and gene therapy manufacturing plants.
Segmental Insights
Product Type Insights
In 2022, the Global Viral Vector and Plasmid DNA Manufacturing Market largest share was held by Plasmid DNA segment and is predicted to continue expanding over the coming years.
Application Insights
In 2022, the Global Viral Vector and Plasmid DNA Manufacturing Market cancer segment to witness robust growth in the forecast period and is predicted to continue expanding over the coming years.
Regional Insights
The North America region dominates the Global Viral Vector and Plasmid DNA Manufacturing Market in 2022. North America, particularly the United States, has a well-developed and mature biopharmaceutical industry. The region is home to numerous biotechnology and pharmaceutical companies with extensive experience in research, development, and manufacturing of biologics, including viral vectors and plasmid DNA.
Recent Developments
- In July 2021, toaddress the rapidly expanding need for plasmid DNA-based medicines andessential mRNA-based vaccinations, Thermo Fisher Scientific Inc., the industryleader in providing science services, launched a new cGMP plasmid DNAproduction facility in Carlsbad, California. Plasmid DNA is being utilizedmore frequently in gene treatments and some vaccines as a therapeuticcomponent. Because of its benefits, such as weak immunogenicity, greatersafety, and ease of fabrication, demand for materials and manufacturingcapacity has skyrocketed worldwide.
- In March 2021, Genopis Inc., the San Diego, California-based producer ofplasmid DNA that Wacker purchased in February, has changed its name to WackerBiotech US Inc. A connected business and a plasmid DNA (pDNA) CDMO site are thesubject of the acquisition. Wacker Biotech US Inc. enhances Wacker's current portfolio by offeringexpertise in pDNA technology and lays the groundwork for future expansion inthe biopharma industry. Wacker Biotech US Inc. also gives Wacker a localfoothold in the biopharmaceuticals sector in the United States.
- In June 2020, A major supplier of goods and services to thebiotechnology sector, Aldevron, recently announced a collaboration withZiopharm Oncology to create plasmid DNA for T cell treatment of solid tumours.To serve this emerging and quickly expanding industry, Aldevron has created theneoGMP service level. According to the agreement, Ziopharm will discover TCRs for each patientindividually and compile TCRs into a library for use in clinical trials basedon their studies of patient tumours. The business will quickly and affordablyproduce many DNA plasmids using Aldevron's neoGMP service. Aldevron produces nucleicacids, proteins, and antibodies on demand for the biotechnology sector. To cure the millions of patients worldwidewho are diagnosed with a solid tumour each year, Ziopharm is creatingnon-viral, cytokine-driven cell and gene therapies that weaponize the body'simmune system. Ziopharm is at the forefront of immuno-oncology with itsmultiplatform strategy and aims to treat any kind of solid tumour. Based on itsnon-viral Sleeping Beauty gene transfer platform, a precisely controlled IL-12gene therapy, and quickly manufactured Sleeping Beauty-enabled CD19-specificCAR-T programme, Ziopharm's pipeline is designed for commercially scalable,cost-effective T cell receptor T cell therapeutics.
Key Market Players
- OxfordBiomedica PLC
- CognateBioServices Inc.
- Cell andGene Therapy Catapult Ltd.
- FinVectorVision Therapies
- FujifilmHoldings Corporation (Fujifilm Diosynth Biotechnologies)
- SIRIONBiotech GmbH
- Merck KGaAInc.
- ThermoFisher Scientific
- Uniqure NV
- CatalentInc.
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