Industry: Medical Care
Published Date: 2025-01-13
Pages: 109 Pages
Report ld: 3503439
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The global market for Viral Vectors Gene Therapy was estimated to be worth US$ million in 2024 and is forecast to a readjusted size of US$ million by 2031 with a CAGR of %during the forecast period 2025-2031.
Viruses have evolved to become highly efficient at nucleic acid delivery to specific cell types while avoiding immunosurveillance by an infected host. These properties make viruses attractive gene-delivery vehicles, or vectors, for gene therapy. Several types of viruses, including retrovirus, adenovirus, adeno-associated virus (AAV), and herpes simplex virus, have been modified in the laboratory for use in gene therapy applications. Because these vector systems have unique advantages and limitations, each has applications for which it is best suited. Retroviral vectors can permanently integrate into the genome of the infected cell, but require mitotic cell division for transduction. Adenoviral vectors can efficiently deliver genes to a wide variety of dividing and nondividing cell types, but immune elimination of infected cells often limits gene expression in vivo.
The global pharmaceutical market is 1475 billion USD in 2022, growing at a CAGR of 5% during the next six years. The pharmaceutical market includes chemical drugs and biological drugs. For biologics is expected to 381 billion USD in 2022. In comparison, the chemical drug market is estimated to increase from 1005 billion in 2018 to 1094 billion U.S. dollars in 2022. The pharmaceutical market factors such as increasing demand for healthcare, technological advancements, and the rising prevalence of chronic diseases, increase in funding from private & government organizations for development of pharmaceutical manufacturing segments and rise in R&D activities for drugs. However, the industry also faces challenges such as stringent regulations, high costs of research and development, and patent expirations. Companies need to continuously innovate and adapt to these challenges to stay competitive in the market and ensure their products reach patients in need. Additionally, the COVID-19 pandemic has highlighted the importance of vaccine development and supply chain management, further emphasizing the need for pharmaceutical companies to be agile and responsive to emerging public health needs.
This report aims to provide a comprehensive presentation of the global market for Viral Vectors Gene Therapy, focusing on the total sales revenue, key companies market share and ranking, together with an analysis of Viral Vectors Gene Therapy by region & country, by Type, and by Application.
The Viral Vectors Gene Therapy market size, estimations, and forecasts are provided in terms of sales revenue ($ millions), considering 2024 as the base year, with history and forecast data for the period from 2020 to 2031. With both quantitative and qualitative analysis, to help readers develop business/growth strategies, assess the market competitive situation, analyze their position in the current marketplace, and make informed business decisions regarding Viral Vectors Gene Therapy.
MARKET SEGMENTATION
CHAPTER OUTLINE
Chapter 1: Introduces the report scope of the report, global total market size. This chapter also provides the market dynamics, latest developments of the market, the driving factors and restrictive factors of the market, the challenges and risks faced by manufacturers in the industry, and the analysis of relevant policies in the industry.
Chapter 2: Detailed analysis of Viral Vectors Gene Therapy company competitive landscape, revenue market share, latest development plan, merger, and acquisition information, etc.
Chapter 3: Provides the analysis of various market segments by Type, covering the market size and development potential of each market segment, to help readers find the blue ocean market in different market segments.
Chapter 4: Provides the analysis of various market segments by Application, covering the market size and development potential of each market segment, to help readers find the blue ocean market in different downstream markets.
Chapter 5: Revenue of Viral Vectors Gene Therapy in regional level. It provides a quantitative analysis of the market size and development potential of each region and introduces the market development, future development prospects, market space, and market size of each country in the world.
Chapter 6: Revenue of Viral Vectors Gene Therapy in country level. It provides sigmate data by Type, and by Application for each country/region.
Chapter 7: Provides profiles of key players, introducing the basic situation of the main companies in the market in detail, including product revenue, gross margin, product introduction, recent development, etc.
Chapter 8: Analysis of industrial chain, including the upstream and downstream of the industry.
Chapter 9: Conclusion.
QYRESEARCH'S STRENGTHS
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TABLE OF CONTENTS
1 Market Overview
1.1 Viral Vectors Gene Therapy Product Introduction
1.2 Global Viral Vectors Gene Therapy Market Size Forecast (2020-2031)
1.3 Viral Vectors Gene Therapy Market Trends & Drivers
1.3.1 Viral Vectors Gene Therapy Industry Trends
1.3.2 Viral Vectors Gene Therapy Market Drivers & Opportunity
1.3.3 Viral Vectors Gene Therapy Market Challenges
1.3.4 Viral Vectors Gene Therapy Market Restraints
1.4 Assumptions and Limitations
1.5 Study Objectives
1.6 Years Considered
2 Competitive Analysis by Company
2.1 Global Viral Vectors Gene Therapy Players Revenue Ranking (2024)
2.2 Global Viral Vectors Gene Therapy Revenue by Company (2020-2025)
2.3 Key Companies Viral Vectors Gene Therapy Manufacturing Base Distribution and Headquarters
2.4 Key Companies Viral Vectors Gene Therapy Product Offered
2.5 Key Companies Time to Begin Mass Production of Viral Vectors Gene Therapy
2.6 Viral Vectors Gene Therapy Market Competitive Analysis
2.6.1 Viral Vectors Gene Therapy Market Concentration Rate (2020-2025)
2.6.2 Global 5 and 10 Largest Companies by Viral Vectors Gene Therapy Revenue in 2024
2.6.3 Global Top Companies by Company Type (Tier 1, Tier 2, and Tier 3) & (based on the Revenue in Viral Vectors Gene Therapy as of 2024)
2.7 Mergers & Acquisitions, Expansion
3 Segmentation by Type
3.1 Introduction by Type
3.1.1 Retro Viral Vectors
3.1.2 Adeno-associated Virus Vectors
3.1.3 Other Viral Vectors
3.2 Global Viral Vectors Gene Therapy Sales Value by Type
3.2.1 Global Viral Vectors Gene Therapy Sales Value by Type (2020 VS 2024 VS 2031)
3.2.2 Global Viral Vectors Gene Therapy Sales Value, by Type (2020-2031)
3.2.3 Global Viral Vectors Gene Therapy Sales Value, by Type (%) (2020-2031)
4 Segmentation by Application
4.1 Introduction by Application
4.1.1 In Vivo
4.1.2 Ex Vivo
4.2 Global Viral Vectors Gene Therapy Sales Value by Application
4.2.1 Global Viral Vectors Gene Therapy Sales Value by Application (2020 VS 2024 VS 2031)
4.2.2 Global Viral Vectors Gene Therapy Sales Value, by Application (2020-2031)
4.2.3 Global Viral Vectors Gene Therapy Sales Value, by Application (%) (2020-2031)
5 Segmentation by Region
5.1 Global Viral Vectors Gene Therapy Sales Value by Region
5.1.1 Global Viral Vectors Gene Therapy Sales Value by Region: 2020 VS 2024 VS 2031
5.1.2 Global Viral Vectors Gene Therapy Sales Value by Region (2020-2025)
5.1.3 Global Viral Vectors Gene Therapy Sales Value by Region (2026-2031)
5.1.4 Global Viral Vectors Gene Therapy Sales Value by Region (%), (2020-2031)
5.2 North America
5.2.1 North America Viral Vectors Gene Therapy Sales Value, 2020-2031
5.2.2 North America Viral Vectors Gene Therapy Sales Value by Country (%), 2024 VS 2031
5.3 Europe
5.3.1 Europe Viral Vectors Gene Therapy Sales Value, 2020-2031
5.3.2 Europe Viral Vectors Gene Therapy Sales Value by Country (%), 2024 VS 2031
5.4 Asia Pacific
5.4.1 Asia Pacific Viral Vectors Gene Therapy Sales Value, 2020-2031
5.4.2 Asia Pacific Viral Vectors Gene Therapy Sales Value by Region (%), 2024 VS 2031
5.5 South America
5.5.1 South America Viral Vectors Gene Therapy Sales Value, 2020-2031
5.5.2 South America Viral Vectors Gene Therapy Sales Value by Country (%), 2024 VS 2031
5.6 Middle East & Africa
5.6.1 Middle East & Africa Viral Vectors Gene Therapy Sales Value, 2020-2031
5.6.2 Middle East & Africa Viral Vectors Gene Therapy Sales Value by Country (%), 2024 VS 2031
6 Segmentation by Key Countries/Regions
6.1 Key Countries/Regions Viral Vectors Gene Therapy Sales Value Growth Trends, 2020 VS 2024 VS 2031
6.2 Key Countries/Regions Viral Vectors Gene Therapy Sales Value, 2020-2031
6.3 United States
6.3.1 United States Viral Vectors Gene Therapy Sales Value, 2020-2031
6.3.2 United States Viral Vectors Gene Therapy Sales Value by Type (%), 2024 VS 2031
6.3.3 United States Viral Vectors Gene Therapy Sales Value by Application, 2024 VS 2031
6.4 Europe
6.4.1 Europe Viral Vectors Gene Therapy Sales Value, 2020-2031
6.4.2 Europe Viral Vectors Gene Therapy Sales Value by Type (%), 2024 VS 2031
6.4.3 Europe Viral Vectors Gene Therapy Sales Value by Application, 2024 VS 2031
6.5 China
6.5.1 China Viral Vectors Gene Therapy Sales Value, 2020-2031
6.5.2 China Viral Vectors Gene Therapy Sales Value by Type (%), 2024 VS 2031
6.5.3 China Viral Vectors Gene Therapy Sales Value by Application, 2024 VS 2031
6.6 Japan
6.6.1 Japan Viral Vectors Gene Therapy Sales Value, 2020-2031
6.6.2 Japan Viral Vectors Gene Therapy Sales Value by Type (%), 2024 VS 2031
6.6.3 Japan Viral Vectors Gene Therapy Sales Value by Application, 2024 VS 2031
6.7 South Korea
6.7.1 South Korea Viral Vectors Gene Therapy Sales Value, 2020-2031
6.7.2 South Korea Viral Vectors Gene Therapy Sales Value by Type (%), 2024 VS 2031
6.7.3 South Korea Viral Vectors Gene Therapy Sales Value by Application, 2024 VS 2031
6.8 Southeast Asia
6.8.1 Southeast Asia Viral Vectors Gene Therapy Sales Value, 2020-2031
6.8.2 Southeast Asia Viral Vectors Gene Therapy Sales Value by Type (%), 2024 VS 2031
6.8.3 Southeast Asia Viral Vectors Gene Therapy Sales Value by Application, 2024 VS 2031
6.9 India
6.9.1 India Viral Vectors Gene Therapy Sales Value, 2020-2031
6.9.2 India Viral Vectors Gene Therapy Sales Value by Type (%), 2024 VS 2031
6.9.3 India Viral Vectors Gene Therapy Sales Value by Application, 2024 VS 2031
7 Company Profiles
7.1 Amgen
7.1.1 Amgen Profile
7.1.2 Amgen Main Business
7.1.3 Amgen Viral Vectors Gene Therapy Products, Services and Solutions
7.1.4 Amgen Viral Vectors Gene Therapy Revenue (US$ Million) & (2020-2025)
7.1.5 Amgen Recent Developments
7.2 Novartis
7.2.1 Novartis Profile
7.2.2 Novartis Main Business
7.2.3 Novartis Viral Vectors Gene Therapy Products, Services and Solutions
7.2.4 Novartis Viral Vectors Gene Therapy Revenue (US$ Million) & (2020-2025)
7.2.5 Novartis Recent Developments
7.3 Orchard Therapeutics
7.3.1 Orchard Therapeutics Profile
7.3.2 Orchard Therapeutics Main Business
7.3.3 Orchard Therapeutics Viral Vectors Gene Therapy Products, Services and Solutions
7.3.4 Orchard Therapeutics Viral Vectors Gene Therapy Revenue (US$ Million) & (2020-2025)
7.3.5 Orchard Therapeutics Recent Developments
7.4 Spark Therapeutics
7.4.1 Spark Therapeutics Profile
7.4.2 Spark Therapeutics Main Business
7.4.3 Spark Therapeutics Viral Vectors Gene Therapy Products, Services and Solutions
7.4.4 Spark Therapeutics Viral Vectors Gene Therapy Revenue (US$ Million) & (2020-2025)
7.4.5 Spark Therapeutics Recent Developments
7.5 Agc Biologics
7.5.1 Agc Biologics Profile
7.5.2 Agc Biologics Main Business
7.5.3 Agc Biologics Viral Vectors Gene Therapy Products, Services and Solutions
7.5.4 Agc Biologics Viral Vectors Gene Therapy Revenue (US$ Million) & (2020-2025)
7.5.5 Agc Biologics Recent Developments
7.6 Anges
7.6.1 Anges Profile
7.6.2 Anges Main Business
7.6.3 Anges Viral Vectors Gene Therapy Products, Services and Solutions
7.6.4 Anges Viral Vectors Gene Therapy Revenue (US$ Million) & (2020-2025)
7.6.5 Anges Recent Developments
7.7 Bluebird Bio
7.7.1 Bluebird Bio Profile
7.7.2 Bluebird Bio Main Business
7.7.3 Bluebird Bio Viral Vectors Gene Therapy Products, Services and Solutions
7.7.4 Bluebird Bio Viral Vectors Gene Therapy Revenue (US$ Million) & (2020-2025)
7.7.5 Bluebird Bio Recent Developments
7.8 Jazz Pharmaceuticals
7.8.1 Jazz Pharmaceuticals Profile
7.8.2 Jazz Pharmaceuticals Main Business
7.8.3 Jazz Pharmaceuticals Viral Vectors Gene Therapy Products, Services and Solutions
7.8.4 Jazz Pharmaceuticals Viral Vectors Gene Therapy Revenue (US$ Million) & (2020-2025)
7.8.5 Jazz Pharmaceuticals Recent Developments
7.9 Dynavax Technologies
7.9.1 Dynavax Technologies Profile
7.9.2 Dynavax Technologies Main Business
7.9.3 Dynavax Technologies Viral Vectors Gene Therapy Products, Services and Solutions
7.9.4 Dynavax Technologies Viral Vectors Gene Therapy Revenue (US$ Million) & (2020-2025)
7.9.5 Dynavax Technologies Recent Developments
7.10 Biogen
7.10.1 Biogen Profile
7.10.2 Biogen Main Business
7.10.3 Biogen Viral Vectors Gene Therapy Products, Services and Solutions
7.10.4 Biogen Viral Vectors Gene Therapy Revenue (US$ Million) & (2020-2025)
7.10.5 Biogen Recent Developments
7.11 Sarepta Therapeutics
7.11.1 Sarepta Therapeutics Profile
7.11.2 Sarepta Therapeutics Main Business
7.11.3 Sarepta Therapeutics Viral Vectors Gene Therapy Products, Services and Solutions
7.11.4 Sarepta Therapeutics Viral Vectors Gene Therapy Revenue (US$ Million) & (2020-2025)
7.11.5 Sarepta Therapeutics Recent Developments
7.12 Gilead Sciences
7.12.1 Gilead Sciences Profile
7.12.2 Gilead Sciences Main Business
7.12.3 Gilead Sciences Viral Vectors Gene Therapy Products, Services and Solutions
7.12.4 Gilead Sciences Viral Vectors Gene Therapy Revenue (US$ Million) & (2020-2025)
7.12.5 Gilead Sciences Recent Developments
8 Industry Chain Analysis
8.1 Viral Vectors Gene Therapy Industrial Chain
8.2 Viral Vectors Gene Therapy Upstream Analysis
8.2.1 Key Raw Materials
8.2.2 Raw Materials Key Suppliers
8.2.3 Manufacturing Cost Structure
8.3 Midstream Analysis
8.4 Downstream Analysis (Customers Analysis)
8.5 Sales Model and Sales Channels
8.5.1 Viral Vectors Gene Therapy Sales Model
8.5.2 Sales Channel
8.5.3 Viral Vectors Gene Therapy Distributors
9 Research Findings and Conclusion
10 Appendix
10.1 Research Methodology
10.1.1 Methodology/Research Approach
10.1.1.1 Research Programs/Design
10.1.1.2 Market Size Estimation
10.1.1.3 Market Breakdown and Data Triangulation
10.1.2 Data Source
10.1.2.1 Secondary Sources
10.1.2.2 Primary Sources
10.2 Author Details
10.3 Disclaimer
TABLE OF FIGURES
List of Tables
List of Figures
KEY QUESTIONS ADDRESSED BY THE REPORT
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The global market for Viral Vectors Gene Therapy was valued at US$ million in the year 2024 and is projected to reach a revised size of US$ million by 2031, growing at a CAGR of %during the forecast period.
Published Date: 2025-01-13
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Viruses have evolved to become highly efficient at nucleic acid delivery to specific cell types while avoiding immunosurveillance by an infected host. These properties make viruses attractive gene-delivery vehicles, or vectors, for gene therapy. Several types of viruses, including retrovirus, adenovirus, adeno-associated virus (AAV), and herpes simplex virus, have been modified in the laboratory for use in gene therapy applications. Because these vector systems have unique advantages and limitations, each has applications for which it is best suited. Retroviral vectors can permanently integrate into the genome of the infected cell, but require mitotic cell division for transduction. Adenoviral vectors can efficiently deliver genes to a wide variety of dividing and nondividing cell types, but immune elimination of infected cells often limits gene expression in vivo.
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Viruses have evolved to become highly efficient at nucleic acid delivery to specific cell types while avoiding immunosurveillance by an infected host. These properties make viruses attractive gene-delivery vehicles, or vectors, for gene therapy. Several types of viruses, including retrovirus, adenovirus, adeno-associated virus (AAV), and herpes simplex virus, have been modified in the laboratory for use in gene therapy applications. Because these vector systems have unique advantages and limitations, each has applications for which it is best suited. Retroviral vectors can permanently integrate into the genome of the infected cell, but require mitotic cell division for transduction. Adenoviral vectors can efficiently deliver genes to a wide variety of dividing and nondividing cell types, but immune elimination of infected cells often limits gene expression in vivo.
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The global market for Viral Vectors Gene Therapy was valued at US$ million in the year 2024 and is projected to reach a revised size of US$ million by 2031, growing at a CAGR of %during the forecast period.
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Viruses have evolved to become highly efficient at nucleic acid delivery to specific cell types while avoiding immunosurveillance by an infected host. These properties make viruses attractive gene-delivery vehicles, or vectors, for gene therapy. Several types of viruses, including retrovirus, adenovirus, adeno-associated virus (AAV), and herpes simplex virus, have been modified in the laboratory for use in gene therapy applications. Because these vector systems have unique advantages and limitations, each has applications for which it is best suited. Retroviral vectors can permanently integrate into the genome of the infected cell, but require mitotic cell division for transduction. Adenoviral vectors can efficiently deliver genes to a wide variety of dividing and nondividing cell types, but immune elimination of infected cells often limits gene expression in vivo.
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Viruses have evolved to become highly efficient at nucleic acid delivery to specific cell types while avoiding immunosurveillance by an infected host. These properties make viruses attractive gene-delivery vehicles, or vectors, for gene therapy. Several types of viruses, including retrovirus, adenovirus, adeno-associated virus (AAV), and herpes simplex virus, have been modified in the laboratory for use in gene therapy applications. Because these vector systems have unique advantages and limitations, each has applications for which it is best suited. Retroviral vectors can permanently integrate into the genome of the infected cell, but require mitotic cell division for transduction. Adenoviral vectors can efficiently deliver genes to a wide variety of dividing and nondividing cell types, but immune elimination of infected cells often limits gene expression in vivo.
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REPORT COVERAGE
DESCRIPTION
OVERVIEW
MARKET SEGMENTATION
CHAPTER OUTLINE
QYRESEARCH'S STRENGTHS
TABLE OF CONTENTS
TABLE OF FIGURES
RLEATED REPORTS
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