The 7 major adeno-associated virus gene therapy markets reached a value of US$ 1.9 Billion in 2023. Looking forward, the publisher expects the 7MM to reach US$ 75.1 Billion by 2034, exhibiting a growth rate (CAGR) of 50.46% during 2023-2034.
The adeno-associated virus gene therapy market has been comprehensively analyzed in this 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.
This 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.
The adeno-associated virus gene therapy market has been comprehensively analyzed in this 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.
This 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
- Base Year: 2023
- Historical Period: 2018-2023
- Market Forecast: 2024-2034
Countries Covered
- United States
- Germany
- France
- United Kingdom
- Italy
- Spain
- Japan
Analysis Covered Across Each Country
- Historical, current, and future epidemiology scenario
- Historical, current, and future performance of the adeno-associated virus gene therapy market
- Historical, current, and future performance of various therapeutic categories in the market
- Sales of various drugs across the adeno-associated virus gene therapy market
Competitive Landscape:
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
- Drug overview
- Mechanism of action
- Regulatory status
- Clinical trial results
- Drug uptake and market performance
Late-Stage Pipeline Drugs
- Drug overview
- Mechanism of action
- Regulatory status
- Clinical trial results
- Drug uptake and market performance
Key Questions Answered in this Report:
Market Insights
- How has the adeno-associated virus gene therapy market performed so far and how will it perform in the coming years?
- What are the markets shares of various therapeutic segments in 2023 and how are they expected to perform till 2034?
- What was the country-wise size of the adeno-associated virus gene therapy market across the seven major markets in 2023 and what will it look like in 2034?
- What is the growth rate of the adeno-associated virus gene therapy market across the seven major markets and what will be the expected growth over the next ten years?
- What are the key unmet needs in the market?
Epidemiology Insights
- What is the number of cases (2018-2034) going for adeno-associated virus gene therapy across the seven major markets?
- What is the number of cases (2018-2034) going for adeno-associated virus gene therapy by age across the seven major markets?
- What is the number of cases (2018-2034) going for adeno-associated virus gene therapy by gender across the seven major markets?
- What is the number of cases (2018-2034) going for adeno-associated virus gene therapy by type across the seven major markets?
- How many patients are diagnosed (2018-2034) with adeno-associated virus gene therapy across the seven major markets?
- What is the size of the adeno-associated virus gene therapy patient pool (2018-2023) across the seven major markets?
- What would be the forecasted patient pool (2024-2034) across the seven major markets?
- What are the key factors driving the epidemiological trend of adeno-associated virus gene therapy?
- What will be the growth rate of patients across the seven major markets?
Adeno-associated Virus Gene Therapy: Current Treatment Scenario, Marketed Drugs and Emerging Therapies
- What are the current marketed drugs and what are their market performance?
- What are the key pipeline drugs and how are they expected to perform in the coming years?
- How safe are the current marketed drugs and what are their efficacies?
- How safe are the late-stage pipeline drugs and what are their efficacies?
- What are the current treatment guidelines for adeno-associated virus gene therapy drugs across the seven major markets?
- Who are the key companies in the market and what are their market shares?
- What are the key mergers and acquisitions, licensing activities, collaborations, etc. related to the adeno-associated virus gene therapy market?
- What are the key regulatory events related to the adeno-associated virus gene therapy market?
- What is the structure of clinical trial landscape by status related to the adeno-associated virus gene therapy market?
- What is the structure of clinical trial landscape by phase related to the adeno-associated virus gene therapy market?
- What is the structure of clinical trial landscape by route of administration related to the adeno-associated virus gene therapy market?
Table of Contents
1 Preface3 Executive Summary6 Patient Journey9 Adeno-associated Virus Gene Therapy - Unmet Needs10 Adeno-associated Virus Gene Therapy - Key Endpoints of Treatment13. Adeno-associated Virus Gene Therapy - Attribute Analysis of Key Marketed and Pipeline Drugs16 Adeno-associated Virus Gene Therapy - Recent Events and Inputs From Key Opinion Leaders18 Appendix
2 Scope and Methodology
4 Adeno-associated Virus Gene Therapy - Introduction
5 Adeno-associated Virus Gene Therapy - Disease Overview
7 Adeno-associated Virus Gene Therapy - Epidemiology and Patient Population
8 Adeno-associated Virus Gene Therapy - Treatment Algorithm, Guidelines, and Medical Practices
11 Adeno-associated Virus Gene Therapy - Marketed Products
12 Adeno-associated Virus Gene Therapy - Pipeline Drugs
14. Adeno-associated Virus Gene Therapy - Clinical Trial Landscape
15 Adeno-associated Virus Gene Therapy - Market Scenario
17 Adeno-associated Virus Gene Therapy Market - SWOT Analysis
Methodology
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Table Information
Report Attribute | Details |
---|---|
No. of Pages | 129 |
Published | May 2024 |
Forecast Period | 2023 - 2034 |
Estimated Market Value ( USD | $ 1.9 Billion |
Forecasted Market Value ( USD | $ 75.1 Billion |
Compound Annual Growth Rate | 39.7% |
Regions Covered | Global |