Gene therapy involves introducing, altering, or replacing genes to treat or prevent diseases. Viral vectors are pivotal in delivering therapeutic genes into target cells, addressing genetic disorders, and offering potential cures for previously incurable conditions. For example, lentiviral vectors have shown assurance in feasting genetic disorders like sickle cell anemia and beta-thalassemia. Viral vectors enhance the immune system's ability to target and destroy cancer cells in cancer treatment. Oncolytic viruses, for instance, are designed to infect and destroy cancer cells while limiting healthy tissues selectively. This application shows promise in various cancer types and is under active research and development.
Viral vectors play a crucial role in neuroscience research by facilitating the delivery of genes into the central nervous system. This enables the study of neuronal function, neurodegenerative diseases, and the development of potential therapies for conditions like Parkinson's and Alzheimer's disease. As the demand for viral vectors escalates, there is a growing emphasis on optimizing production processes to achieve scalability and cost-effectiveness. Innovations in bioprocessing technologies, such as single-use systems and high-density cell culture platforms, are streamlining the manufacturing of viral vectors, ensuring a robust and reliable supply chain.
North America, particularly the United States, is a biopharmaceutical research and development hub. The region sees substantial investments from both public and private sectors in developing advanced therapies, including gene therapies and vaccines, boosting the demand for viral vectors. North America has a well-established biotechnology and pharmaceutical infrastructure, with numerous companies specializing in viral vector production. Thus, the above aspects will expand the market growth across the region in the upcoming years.
The US market dominated the North America Viral Vector Production Market, by Country in 2022, and would continue to be a dominant market till 2030; thereby, achieving a market value of $1,164.5 Million by 2030. The Canada market is experiencing a CAGR of 20.6% during (2023 - 2030). Additionally, The Mexico market would exhibit a CAGR of 19.6% during (2023 - 2030).
Based on Type, the market is segmented into Adeno-Associated Viral Vectors, Lentiviral Vectors, Adenoviral Vectors, Retroviral Vectors, and Others. Based on Indication, the market is segmented into Cancer, Genetic Disorders, Infectious Diseases, and Others. Based on Application, the market is segmented into Gene Therapy, and Vaccinology. Based on countries, the market is segmented into U.S., Mexico, Canada, and Rest of North America.
List of Key Companies Profiled
- Andelyn Biosciences, Inc.
- Charles River Laboratories International, Inc.
- Danaher Corporation
- FinVector Oy (Ferring Ventures S/A)
- Thermo Fisher Scientific, Inc.
- Novartis AG
- Takara Bio Inc. (Takara Holdings Inc.)
- Avid Bioservices, Inc.
- Oxford Biomedica plc
- Lonza Group Ltd.
Market Report Segmentation
By Type- Adeno-Associated Viral Vectors
- Lentiviral Vectors
- Adenoviral Vectors
- Retroviral Vectors
- Others
- Cancer
- Genetic Disorders
- Infectious Diseases
- Others
- Gene Therapy
- Vaccinology
- US
- Canada
- Mexico
- Rest of North America
Table of Contents
Companies Mentioned
- Andelyn Biosciences, Inc.
- Charles River Laboratories International, Inc.
- Danaher Corporation
- FinVector Oy (Ferring Ventures S/A)
- Thermo Fisher Scientific, Inc.
- Novartis AG
- Takara Bio Inc. (Takara Holdings Inc.)
- Avid Bioservices, Inc.
- Oxford Biomedica plc
- Lonza Group Ltd.
Methodology
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