Adeno Associated Virus Vectors Manufacturing Market - By Therapeutic Area (Neurological, Metabolic, Ophthalmic, Muscular/Neuromuscular, Infectious, Bleeding), Application (Vaccine, Cell Therapy), Method (In vivo, In vitro), Global Forecast, 2023-2032
Published Date: July - 2024 | Publisher: MIR | No of Pages: 240 | Industry: Healthcare | Format: Report available in PDF / Excel Format
View Details Buy Now 2890 Download Sample Ask for Discount Request CustomizationAdeno Associated Virus Vectors Manufacturing Market size
Adeno Associated Virus Vectors Manufacturing Market size recorded USD 769.7 million in 2022 and is poised to witness growth at CAGR of 22.4% to reach USD 6.1 billion by 2032.
The growth is attributed to factors such as expanding pipeline of gene therapy, increasing, advancements in vector production technology, and increased diversification of therapeutic areas. gene therapy has gained significant attention as a potential treatment for various genetic and acquired diseases. AAV vectors are a preferred choice for gene therapy due to their safety profile, ability to target specific tissues, and low immunogenicity. Also, regulatory agencies such as the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA) have provided clearer pathways and support for the development and approval of AAV-based therapies, thereby fostering industry expansion.
An adeno associated virus (AAV) vector manufacturing is a crucial process in the production of AAV vectors, which are widely used in gene therapy and gene editing applications. AAV vectors are attractive tools for gene delivery due to their safety profile and ability to efficiently transduce various cell types. The complex process of producing AAV vectors involves multiple stages, from the initial design and construction of the viral vector to the final purification and quality control of the vector product.
| Report Attribute | Details |
|---|---|
| Base Year | 2022 |
| Adeno Associated Virus Vectors Manufacturing Market Size in 2022 | USD 769.7 Million |
| Forecast Period | 2023 to 2032 |
| Forecast Period 2023 to 2032 CAGR | 22.4% |
| 2032 Value Projection | USD 6.1 Billion |
| Historical Data for | 2018 to 2022 |
| No. of Pages | 120 |
| Tables, Charts & Figures | 209 |
| Segments covered | Therapeutic Area, Application, Method, and Region |
| Growth Drivers |
|
| Pitfalls & Challenges |
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COVID-19 Impact
The global supply chain disruptions had a notable impact on the availability of essential materials and components required for the manufacturing of AAV vectors. As a result, the production of AAV vectors experienced delays and shortages. However, the urgent need for COVID-19 vaccines drew attention to the biopharmaceutical sector, including gene therapy and vector manufacturing. This highlighted the significance of advanced vaccine technologies, such as viral vectors like AAV. Also, numerous biopharmaceutical companies and contract manufacturing organizations (CMOs) made substantial investments to enhance their AAV vector manufacturing facilities.
These investments primarily aimed to increase production capacity and meet the rising demand for vaccines and gene therapies, including potential COVID-19 treatments. In summary, the COVID-19 pandemic had a positive impact on the global adeno-associated virus (AAV) vector manufacturing market by fostering progress, driven by increased investments and attention brought to the field due to the urgent need for advanced vaccine technologies.
Adeno Associated Virus Vectors Manufacturing Market Trends
The market has experienced significant growth in recent years. The expanding pipeline of gene therapy has generated a surge in demand for adeno-associated virus (AAV) vectors, underscoring their pivotal role in this field. Researchers and biopharmaceutical companies are actively developing and testing new gene therapies for a wide range of conditions, including inherited genetic disorders, rare diseases, neurodegenerative disorders, and certain types of cancer. Each of these therapies typically requires a specific AAV vector tailored to the unique characteristics of the therapeutic gene and the target cells or tissues within the body Therefore, due to the safety and efficacy of AAV vectors, they have gained prominence in gene therapy and genetic medicine, thereby driving the market demand.
Adeno Associated Virus Vector (AAV) Manufacturing Market Restraining Factors
Several factors can impede the market, including stringent regulatory mandates and challenges related to production and scalability. The manufacturing of AAV vectors is a technically complex and resource-intensive process. Ensuring consistency and quality requires meticulous control over production processes, which can result in elevated costs and constraints on scalability. Furthermore, as the demand for AAV vectors increases, scaling up production to meet the requirements of clinical trials and commercialization becomes progressively more challenging. An ongoing hurdle involves the development of large-scale manufacturing procedures that can uphold the quality of the vectors.
Adeno Associated Virus Vectors Manufacturing Market Analysis
Different diseases and conditions are treated using a variety of adeno-associated virus (AAV) vectors. These includeBrain and nerve disordersThis is the biggest area where AAV vectors are used. They're used to deliver genes that can treat different neurological diseases, like Parkinson's and Alzheimer's. Metabolic disorders These are diseases that affect how the body uses energy. AAV vectors can deliver genes that can help the body break down and use energy better. Eye disordersAAV vectors are used to treat eye diseases, such as vision loss. Muscle disorders These are diseases that affect the muscles. AAV vectors can deliver genes that can help strengthen the muscles. Infectious diseasesAAV vectors are used to deliver genes that can fight infections, like HIV. Bleeding disorders These are diseases that affect the blood's ability to clot. AAV vectors can deliver genes that can help the blood clot better. Inflammation and scarring AAV vectors can deliver genes that can help reduce inflammation and scarring. In 2022, brain and nerve disorders were the most common area where AAV vectors were used. This is because AAV vectors are very good at delivering genes to the nervous system. They can either add the gene to the body's DNA or just stay in the body as separate pieces. This means that the treatment can last a long time, which is important for treating brain and nerve disorders.
Based on application, the adeno associated virus vectors manufacturing market is categorized into vaccine, cell therapy, gene therapy, and other applications. The gene therapy segment is expected to reach USD 4.1 billion by 2032. The manufacturing process for AAV vectors, specifically designed for gene therapy applications, entails the large-scale production and purification of these viral vectors to ensure both safety and effectiveness. These manufacturing procedures have been meticulously developed and honed to accommodate substantial production volumes, rendering them well-suited for the clinical and commercial deployment of gene therapies. Thus, aforementioned factors are expected to spur the segment growth.
The adeno-associated virus (AAV) market for gene therapy has two main ways of making these virusesinside living organisms (in vivo) or outside living organisms (in vitro). In 2022, the in vivo method was way ahead, with a market size of $521.7 million. Plus, it's expected to grow super fast, at a rate of 21.8% each year until [add the end of the analysis period]. This in vivo method is the go-to choice for gene therapy, which involves using AAV vectors to treat diseases by replacing or correcting faulty genes. Making AAV vectors for in vivo gene therapy is a tricky process. Scientists have to create and clean these viral vectors very carefully to make sure they're safe, work well, and are the same every time. Over time, this process has gotten better and better, so now it's reliable for using AAV vectors in treatments for gene therapy in both clinical trials and real-world use.
Get ready for a gene therapy revolution! The U.S. market for adeno-associated viral (AAV) vectors, tiny helpers that deliver gene medicine to the body, is about to explode. It's estimated to reach a whopping 3 billion dollars by 2032. North America is leading the charge, playing a big role in testing and bringing to market gene therapies that use AAV vectors. They're tackling all kinds of genetic disorders and diseases with these clinical trials, showing how dedicated they are to advancing gene therapy. The U.S. has the research know-how and the manufacturing muscle to be a major player in making AAV vectors. That's why it's a hub for gene therapy production, making it a game-changer in the global fight against genetic diseases.
Adeno Associated Virus Vectors Manufacturing Market Share
In the realm of AAV vector manufacturing, several notable companies have established themselves as key players, each contributing to the dynamic landscape of gene therapy. Lonza, Thermo Fisher Scientific and Catalent, Inc are prominent entity in this sector, offers an extensive array of services encompassing process development, manufacturing, and analytical testing for AAV vectors. These companies, along with numerous others, collectively contribute to the advancement and growth of the AAV vector manufacturing market, underlining their critical role in the evolution of gene therapy and its potential to transform the landscape of medical treatments.
Market players operating in adeno associated virus vectors manufacturing is as mentioned below
- F. Hoffmann-La Roche (Spark Therapeutics)
- Biomarin Pharmaceutical
- Oxford BioMedica plc
- WuXi AppTec
- YPOSKESI
- Sarepta Therapeutics
- Regenxbio Inc.
- Audentes Therapeutics
- 4D Molecular Therapeutics
- Ultragenyx Pharmaceutical Inc.
Adeno Associated Virus Vectors Manufacturing Industry News
- In September 2021, Regenxbio and AbbVie announced partnership with each other for developing and commercializing RGX-314 that consist of NAV AAV8 vector, a gene therapy for treating wet age-related macular degeneration (wet AMD), diabetic retinopathy (DR) and other chronic retinal diseases. This strategic collaboration helped the company to enhance their R&D, clinical development and increase customer base.
- In January 2020, WuxiAppTec launched new AAV vector suspension platform to help accelerate the process of cell and gene therapy development and manufacturing. This expansion of its service capabilities helped the company to enhance its services and boost its revenue.
The adeno associated virus vectors manufacturing market research report includes an in-depth coverage of the industry with estimates & forecast in terms of revenue in USD Million from 2018 to 2032 for the following segments
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By Therapeutic Area
- Neurological disorders
- Metabolic disorders
- Ophthalmic disorders
- Muscular/Neuromuscular disorders
- Infectious diseases
- Bleeding disorders
- Inflammation and fibrosis
- Other therapeutic areas
By Application
- Gene therapy
- Vaccine
- Cell therapy
- Other applications
By Method
- In vitro
- In vivo
The above information is provided for the following regions and countries
- North America
- U.S.
- Canada
- Europe
- Germany
- UK
- France
- Spain
- Italy
- Rest of Europe
- Asia Pacific
- China
- Japan
- India
- Australia
- Rest of Asia Pacific
- Latin America
- Brazil
- Mexico
- Rest of Latin America
- Middle East & Africa
- South Africa
- Saudi Arabia
- Rest of Middle East & Africa
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