The 7 major adeno-associated virus gene therapy markets reached a value of US$ 1.9 Billion in 2023. Looking forward, IMARC Group expects the 7MM to reach US$ 75.1 Billion by 2034, exhibiting a growth rate (CAGR) of 39.93% during 2024-2034.
Report Attribute
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Key Statistics
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Base Year | 2023 |
Forecast Years | 2024-2034 |
Historical Years |
2018-2023
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Market Size in 2023
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US$ 1.9 Billion |
Market Forecast in 2034
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US$ 75.1 Billion |
Market Growth Rate 2024-2034
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39.93% |
The adeno-associated virus gene therapy market has been comprehensively analyzed in IMARC’s new report titled “Adeno-associated Virus Gene Therapy Market: Epidemiology, Industry Trends, Share, Size, Growth, Opportunity, and Forecast 2024-2034”. Adeno-associated virus (AAV) gene therapy is a type of gene therapy that utilizes adeno-associated virus to deliver genetic material to cells in the body. AAVs are small, non-pathogenic viruses that can infect both dividing and non-dividing cells, making them a useful vector for gene therapy. The ability to generate recombinant AAV particles lacking any viral genes and containing DNA sequences of interest is one of the most actively investigated gene therapy vehicles. Currently, there are two classes of recombinant AAVs (rAAVs) in use: self-complementary AAV (scAAV) and single-stranded AAV (ssAAV). Recombinant adeno-associated virus gene therapy comprises gene silencing, gene replacement, gene addition, and gene editing. AAVs exist in 12 naturally occurring serotypes (AAV serotypes 1 [AAV-1] to AAV-12] and more than 100 variations, each of which has a unique amino acid sequence, especially within the hypervariable regions of the capsid proteins, and thus, also differ slightly in their gene delivery properties. AAVs are also relatively easy to produce and purify, making them a cost-effective gene therapy option. AAV gene therapy offers several benefits, including targeted delivery, long-term effectiveness, low toxicity, the potential for a one-time treatment, etc.
The increasing ability of AAV gene therapy to treat a broad array of disorders, including inherited diseases, certain types of cancer, and numerous viral infections, is primarily driving the global adeno-associated virus gene therapy market. In addition to this, the emerging popularity of the AAV vector owing to its several unique features that are beneficial in clinical applications, including low immunogenicity, broad tropism, and ease of production, is further creating a positive outlook for the market. AAV is also non-pathogenic, rarely integrates into the host chromosome, and results in long-term expression of the transgene. Moreover, various key players are extensively investing in AAV gene therapy research and development activities for the high-yield producer cell lines, which would enable improved quality and more flexible viral-vector production at a lower cost. This, in turn, is further acting as a significant growth-inducing factor. Additionally, the escalating utilization of AAV gene therapy for personalized treatment since it can be easily tailored to the patient’s specific genetic mutation, leading to more effective treatment, is also bolstering the global market. Furthermore, continuous advancements in the biotechnological and genetics sectors, such as modifying AAV transduction efficiency by optimizing the transgene cassette and utilizing capsid engineering to increase vector tropism, are expected to drive the global adeno-associated virus gene therapy market in the coming years.
IMARC Group’s new report provides an exhaustive analysis of the adeno-associated virus gene therapy market in the United States, EU5 (Germany, Spain, Italy, France, and United Kingdom) and Japan. This includes treatment practices, in-market, and pipeline drugs, share of individual therapies, market performance across the seven major markets, market performance of key companies and their drugs, etc. The report also provides the current and future patient pool across the seven major markets. According to the report the United States has the largest patient pool for adeno-associated virus gene therapy and also represents the largest market for its treatment. Furthermore, the current treatment practice/algorithm, market drivers, challenges, opportunities, reimbursement scenario and unmet medical needs, etc. have also been provided in the report. This report is a must-read for manufacturers, investors, business strategists, researchers, consultants, and all those who have any kind of stake or are planning to foray into the adeno-associated virus gene therapy market in any manner.
Time Period of the Study
Countries Covered
Analysis Covered Across Each Country
This report also provides a detailed analysis of the current adeno-associated virus gene therapy marketed drugs and late-stage pipeline drugs.
In-Market Drugs
Late-Stage Pipeline Drugs
Drugs | Company Name |
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Luxturna (voretigene neparvovec-rzyl) | Spark Therapeutics, Inc. |
Zolgensma (onasemnogene abeparvovec) | Novartis Gene Therapies, Inc. |
Glybera (alipogene tiparvovec) | uniQure |
BBM-H901 | Shanghai Belief-Delivery BioMed Co., Ltd |
Valoctocogene Roxaparvovec | BioMarin Pharmaceutical |
RP-A501 | Rocket Pharmaceuticals Inc. |
FBX-101 | Forge Biologics, Inc |
RGX-314 | REGENXBIO Inc. |
*Kindly note that the drugs in the above table only represent a partial list of marketed/pipeline drugs, and the complete list has been provided in the report.
Market Insights
Epidemiology Insights
Adeno-associated Virus Gene Therapy: Current Treatment Scenario, Marketed Drugs and Emerging Therapies