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Global Cell & Gene Therapy Business and Investment Opportunities - Analysis & Market Size by Technology, Clinical Trials, Patents, Financial Deals, Competitive Landscape - Q2 2023 Update

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    Report

  • 1350 Pages
  • August 2023
  • Region: Global
  • BioIntel360
  • ID: 5741415
According to the publisher, global cell and gene therapy market size is expected to record a CAGR of 20.4% during 2023-2027 to reach US$54.490 billion by 2027, increasing from US$21.506 billion in 2023. Over the last five years, the sector has recorded a CAGR of 26.0% to reach US$17.069 billion in 2022.

The lives of people all over the world have been improved by traditional methods of patient treatment that use drugs and surgery, yet there are many diseases possibly even most of them for which these conventional methods only slow the progression of the illness without curing it. This flaw is especially evident when treating monogenic diseases, which are congenital illnesses brought on by single-gene abnormalities.

More than 30 million people in the United States are thought to be affected by one of the more than 7,000 rare diseases that exist. Cells and genetically modified cells are "living drugs" that may repair and replace damaged tissues or ill organs, which makes them fundamentally different from medications and surgery. Due to these characteristics, they may be used to treat a variety of conditions.

There are presently six FDA-approved CAR-T cell therapies available to patients in the United States and Europe to treat different types of blood cancers. These are quite promising therapies that are being developed for both rare and common disorders.

A glimmer of hope for patients waiting for long-term, potentially curative treatments is the fact that more than 1,000 clinical trials, including 200 in Phase III, are now under progress. Phase I/II combo studies are frequently used. Because it enables sponsors to improve and accelerate their clinical development programmes, this design approach is still being used more and more in the industry. The industry must overcome funding, regulatory, and legislative barriers, and many patients won't benefit unless we transform the way we provide healthcare.

An expansion of the CGT pipeline expects increased global cell and gene therapy market growth

The year 2022 marked a turning point for the licencing of never-before-approved gene treatments, with three new medications licenced to treat uncommon illnesses and another authorised to treat bladder cancer. This is just the first wave of the transforming ripple. By the end of 2023, innovative cell or gene therapies may have received approval for use in Europe, the United States, or both. The industry is on the verge of achieving the FDA's widely reported 2,019 forecast that 10-20 innovative cell and gene therapies will be approved annually by 2025.
  • In December 2022 a chimeric antigen receptor (CAR) T-cell therapy called Yescarta (axicabtagene ciloleucel) has been approved by the Japanese Ministry of Health, Labour and Welfare (MHLW) for the initial treatment of patients with relapsed/refractory large B-cell lymphoma (R/R LBCL), including those with diffuse large B-cell lymphoma and primary mediastinal large B-cell lymphoma, transformed follicular lymphoma, and high-grade B-cell lymphoma.
  • Yescarta® (axicabtagene ciloleucel), a CAR T-cell treatment, was given FDA approval in April 2022 for treating adult patients with large B-cell lymphoma.
  • The European Commission (EC) approved Kymriah® (tisagenlecleucel), a CAR-T cell therapy, for the treatment of adult patients with relapsed or refractory (r/r) follicular lymphoma (FL) after two or more lines of systemic therapy, according to Novartis.
  • Commercial demand for Abecma (idecabtagene vicleucel) remained strong into 2022. In addition to increasing manufacturing capacity, 2seventy bio and BMS made major advancements in key supply chain indicators.
  • In 2023, the company projects topline U.S. sales of $470-$570M thanks to further expansions in the manufacturing capacity of vector and pharmacological products, including an extra adherent vector manufacturing suite. 2seventy Bio anticipates additional commercial growth with an anticipated label expansion in 2024-2025. With this expansion, 2seventybio anticipates that Abecma will produce $200-300M in operational income for 2seventybio between 2024 and 2025.
  • The first cell-based gene therapy, Zynteglo (betibeglogene autotemcel), has been given the green light by the US Food and Drug Administration to treat adult and paediatric beta-thalassemia patients who need regular red blood cell transfusions

In the future, it's anticipated that M&A activity will increase in cell and gene therapy market

  • In the field of CGT, where licencing and cooperative arrangements continue to dominate. This is hardly surprising given the relative youth of CGT technology, as there are still questions about values and technical obstacles. Partnerships give the licensor or investor a reduced risk way to increase CGT offerings without taking on full financial responsibility or experiencing the productivity disruption frequently associated with M&A.
  • Investments are going into firms of all stages of development, from start-ups to significant acquisitions by big pharmaceutical firms. In 2019, to purchase Celgene, Bristol Myers Squibb paid $74 billion. The largest of them are involved in oncology treatments.
  • Cell and gene therapy market draws an increased amount and share of public and private investment despite the limited number of licenced products. Despite the fact that during the past ten years, all private sector investment in the life sciences has increased significantly, the exponential growth of overall investments in cell and gene therapy firms is extraordinary.
  • Neogene Therapeutics, a global clinical-stage biotechnology firm that is leading the discovery, development, and production of next-generation T-cell receptor treatments (TCR-Ts), which provide a unique cell therapy strategy for treating cancer, has announced that AstraZeneca is acquiring it.
Growing cell and gene therapy enterprises have received support from this surge in private money as they reach the stock market. Initially, it showed early growth but later it went through a period of severe distortions during the pandemic. It is expected that cell and gene firms return to a more measured growth trajectory, underpinned by a growing number of clinical milestones and perhaps more regulatory approvals, as stock markets adapt and the economy picks up through the projected period.

European region may regain its feet in the field of cell and gene therapy with regulatory checks

  • Although authorities in the US and Europe are moving forward with reforming their regulatory frameworks in response to scientific advancements, barriers to patient access remain a major issue in both places.
  • The European Union will update its pharmaceuticals legislation; the proposal is anticipated in the first quarter of 2023. The project will have a significant impact on whether European patients have access to advanced therapy medicinal products for years to come by balancing affordability and access, among other issues.
  • Europe faces tremendous challenges, particularly when it comes to access. Having the European Medicines Agency, a top-notch regulatory organisation, and having approved the first gene therapy, Europe has been a tremendous pioneer in the sector in many ways. However, due to a combination of complex factors, Europe is already lagging on certain crucial fronts.

Regulatory trends that will shape the future of the cell and gene therapy market

  • In the upcoming years, it is anticipated that filing application numbers would rise. The amount of requests for Breakthrough (BT) and Regenerative Medicine Advanced Therapy (RMAT) designations, which are submitted concurrently with or during an ongoing IND file, has recently increased. While the benefits of BT and RMAT designations are comparable to those of fast-track designation, these designations also call for more robust supporting documentation.
  • Within the framework of the NIH Accelerating Medicines Partnership Program, the FDA recently launched a new effort. The Bespoke Gene Therapy Consortium (BGTC) was established to remove significant barriers and streamline the small-batch gene therapy research process. By giving details on basic and clinical research, manufacturing, production, and regulatory needs, the BGTC will serve as a traffic light for these therapies.
  • The FDA's "INTERACT" casual meeting programme is a relatively new project. This initiative involves informal talks between the Center for Biologics Evaluation and Research (CBER) employees and researchers/sponsors who are in the pre-IND stage of development to address the concerns and demands faced by the CGT industry within current clinical guidelines. The INTERACT meetings do not charge anything under the Prescription Drug User Fee Act (PDUFA). They are given based on CBER's resources and availability, and they do not take the place of other official meetings. Therefore, it is advised to ask for a pre-IND meeting before submitting an IND to start the Phase I first-in-human investigation. This is crucial when looking for advice on the designs of toxicity study plans.
  • The FDA has just launched the Gene Therapy Pilot Program, which entails giving sponsors input in real-time throughout the clinical development process. The development cycle and submission review time should be sped up by the combination of new meeting formats. Together, these programmes provide opportunities for sponsors and regulators to speak and debate technical advancements more frequently.
To ensure that patients benefit from this technology, however, there are crucial challenges that exist within the cell and gene therapy market and they must be resolved. Industry and the healthcare sector are prepared to invest in the CGT ecosystem and have faith that long-term problems (such as costs, safety, and reimbursement) will be resolved.

Firms in the cell and gene therapy market and their investors should understand and distinguish marketing hype from legitimate science. This is a new market with enormous potential opportunities, but it still carries many risks until it is economically established. The potential of CGT to usher in a new era of medicine has undoubtedly inspired a lot of optimism globally

This report presents an in-depth analysis of the current cell and gene therapy market scenario, with an emphasis on the future trajectory of potential opportunities in the cell and gene therapy industry. In addition to a combination of exhaustive secondary research along with primary research, the publisher's research methodology leverages a proprietary predictive analytics platform to provide unbiased business intelligence and answer key questions related to the cell and gene therapy market forecast.

It provides a detailed analysis of cell and gene therapy market dynamics, covering clinical trials, patent data, financial deals, and company profiling details. It details market opportunities and risks across key segments - by type of therapy segment, by the purpose of manufacturing, by type of cell, by product, by route of administration, delivery mode, source of cell, source of manufacturing, therapeutic class, technology, and by type of therapy. It also details market dynamics across various end-use sectors to assess emerging opportunities.

In addition, this report provides analyst commentary on key trends, drivers, strategies, innovations, and regulations in the cell and gene therapy market.

This title provides global and regional insights along with data-centric analysis for the following 6 regions and 20 countries:

  • Global
  • North America
  • United States
  • Canada
  • Mexico
  • Europe
  • United Kingdom
  • France
  • Germany
  • Italy
  • Netherlands
  • Asia-Pacific
  • China
  • Japan
  • Australia
  • India
  • South Korea
  • Latin America
  • Brazil
  • Argentina
  • Colombia
  • MEA
  • Israel
  • South Africa
  • UAE
  • Saudi Arabia

Scope

Insights and data in the report have been segmented under the following six modules:

Module 1: Global Cell and Gene Therapy Funding and Investments Outlook

This module provides insights and data related to cell and gene therapy partnerships and investment (research and development, mergers and acquisitions, product development, commercialization, licensing, and manufacturing) and allows a peek into the futuristic trends of cell and gene therapy technology investment area.

Module 2: Global Cell and Gene Therapy Clinical Trial Data Assessment

This module evaluates the data available from clinical trials conducted in this sector, representing a bird’s eye view of emerging market dynamics and risks in the cell and gene therapy sector.

Module 3: Global Cell and Gene Therapy Patent Data Analysis

This module presents an exhaustive study of cell and gene therapy patent analytics at various levels, including strategic research planning as well as analyzing their potential applications.

Module 4: Competitive Landscape

This module provides detailed information along with a scoring matrix of key companies related to the cell and gene therapy industry, including their historical performance and the latest developments.

Module 5: Global Cell and Gene Therapy Market Size and Forecast

This module provides projections on the market's development during the years 2018-2027 after the profound evaluation of market dynamics at the deeper segmentation level. This report also provides an in-depth, data-centric analysis of the global cell and gene therapy market at regional and country levels:

Cell & Gene Therapy Market Size by Different Therapy Segment, 2018-2027

  • Cell and Gene Modified Cell Therapies
  • Gene Therapy and Genome Therapy
  • DNA & RNA Therapeutics

Cell & Gene Therapy Market Size by Purpose of Manufacturing

  • Commercial
  • Clinical

Cell & Gene Therapy Market Size by Product

  • Abecma
  • Amondys
  • Breyanzi
  • Carvykti
  • Givlaari
  • Kimmtrak
  • Kymriah
  • Leqvio
  • Luxturna
  • Onpattro
  • Oxlumo
  • Rethymic
  • Skysona
  • Stratagraft
  • Tecartus
  • Tegsedi
  • Viltepso
  • Vyondys
  • Yescarta
  • Zolgensma
  • Zynteglo

Cell & Gene Therapy Market Size by Route of Administration

  • Injectables
  • Infusions
  • Bioscaffolds
  • Topicals

Cell & Gene Therapy Market Size by Type of Cell

  • CAR-T Cell
  • TCR Cell

Cell & Gene Therapy Market Size by Type of Therapy

  • T-Cell Therapies
  • NK Cell
  • Dendritic Cell Therapies
  • Stem Cell Therapies

Cell & Gene Therapy Market Size by Source of Cell

  • Autologous
  • Allogenic

Cell & Gene Therapy Market Size by Delivery Mode

  • In vivo
  • ex-vivo

Cell & Gene Therapy Market Size by Source of Manufacturing

  • In-House
  • Contract Manufacturing

Cell & Gene Therapy Market Size by Therapeutic Class

  • Oncology
  • Neurology
  • Ophthalmology
  • Musculoskeletal
  • Others

Cell & Gene Therapy Market Size by Technology

  • Viral Vector Technology
  • Cell Immortalization Technology
  • Genome Editing Technology
  • Others

Cell & Gene Therapy Market Size by End User

  • Pharmaceutical & Biotechnology Companies
  • Academic & Research Institutes
  • Hospital & Clinics

Cell & Gene Therapy Market Size by Regions

  • North America
  • U. S.
  • Canada
  • Mexico
  • Europe
  • France
  • United Kingdom
  • Germany
  • Italy
  • Netherlands
  • Asia-Pacific
  • China
  • Japan
  • Australia
  • India
  • South Korea
  • MEA region
  • Israel
  • South Africa
  • U.A. E
  • North America
  • Latin America
  • Brazil
  • Argentina
  • Colombia

Key Companies Covered

  • Gilead Company
  • Novartis
  • Roche Holding AG
  • Johnson & Johnson
  • Bristol Myers Squibb
  • bluebird bio
  • Alnylam Pharmaceuticals

Module 6 Regulatory Outlook

This module contains a detailed understanding of the ethical, legal, and social implications of cell and gene therapy technology.

Reasons to buy

  • Cell & Gene Therapy Market Dynamics: Understand market opportunities and key trends along with forecast (2023-2027). Understand market dynamics across various segments such as by type of therapy, the purpose of manufacturing, type of cell, product, route of administration, delivery mode, source of cell, source of manufacturing, therapeutic class, technology, end-user, by-products, delivery, geographical region, and company profiling.
  • Competitive Landscape Analysis: Market position and snapshot of key players in the development of cell and gene therapies. Each profile includes a brief overview of the company, information on its therapeutic pipeline, financial data (where available), the most recent events, and future direction of the market.
  • Clinical Trial Analysis: Insights into opportunities across cell and gene-based therapies that have been completed or are still ongoing, using parameters such as trial status, trial registration year, an indication of the target disease, trial phase, patient enrolment, and sponsor/collaborator type.
  • Develop Market-Specific Strategies: Identify growth segments based on a thorough analysis of the cell & gene therapy patents that have been applied for or granted based on the patent type, the issuing agency, and patent offices involved, the Cooperative Patent Classification (CPC) symbols, the firm type, significant industry and non-industry participants (based on many patents), and discrete patent assignees.
  • Financial Deals Insights: Get insights into various cell and gene therapy partnerships that have been developed, including those for research and development (R&D), clinical trials, mergers and acquisitions, product development, commercialization, licencing, and manufacturing. A complete analysis of the various investments made in companies that specialise in developing drugs using cell and gene therapy technologies.
Frequently Asked Questions about the Global Cell & Gene Therapy Market

What is the estimated value of the Global Cell & Gene Therapy Market?

The Global Cell & Gene Therapy Market was estimated to be valued at $21.51 Billion in 2023.

What is the growth rate of the Global Cell & Gene Therapy Market?

The growth rate of the Global Cell & Gene Therapy Market is 20.4%, with an estimated value of $54.49 Billion by 2027.

What is the forecasted size of the Global Cell & Gene Therapy Market?

The Global Cell & Gene Therapy Market is estimated to be worth $54.49 Billion by 2027.

Who are the key companies in the Global Cell & Gene Therapy Market?

Key companies in the Global Cell & Gene Therapy Market include Gilead Company, Novartis, Bristol Myers Squibb, bluebird bio, Johnson & Johnson, Roche Holding AG and Alnylam Pharmaceuticals.

Table of Contents

Chapter 1 About this Report
1.1 Research Methodology
1.2 Definitions
1.3 Disclaimer
Chapter 2 Global Cell and Gene Therapy Market Outlook and Future Growth Dynamics
2.1 Introduction
2.2 Market Opportunities and Growth Dynamics
2.3 Strategy and Innovations
2.4 Regulation and Challenges Related to Cell and Gene Therapy Around the Globe
Chapter 3 Regulatory Dynamics Assessment Across Different regions
3.1 North America Cell and Gene Therapy Regulations
3.2 Europe Cell and Gene Therapy Regulations
3.3 Asia Pacific Cell and Gene Therapy Regulations
3.4 Latin America Cell and Gene Therapy Regulations
3.5 Middle East & Africa region Cell and Gene Therapy Regulation
Chapter 4 Global Cell and Gene Therapy Discovery and Clinical Pipeline Market Attractiveness
4.1 Cell and Gene Therapy Based: Discovery and Clinical Pipeline, 2023
4.2 Cell and Gene Therapy Based: Discovery and Clinical Pipeline, 2024
4.3 Cell and Gene Therapy Based: Discovery and Clinical Pipeline, 2025-2027
4.4 Approved Cell and Gene Therapies, 2017-2022
4.5 Anticipated Regulatory Decisions, 2023
4.6 Predicted Cell and Gene Therapy Product Launches, 2018-2030
4.7 List of Top 10 Innovation Driving Worldwide CGT Sales in 2022
4.8 FDA Approved Cell and Gene Therapies
Chapter 5 Global Cell and Gene Therapy Financial Deals & Alliances Market Dynamics & Outlook
5.1 Cell and Gene Therapy Financial Deals & Alliances Market Prediction and Estimation
5.2 Cell and Gene Therapy Financial Deals Vs Mergers & Acquisition, 2022 vs 2025
5.3 Cell and Gene Therapy Financial Deals Analysis by Different Therapy Segment, 2022 vs 2025
5.4 Cell and Gene Therapy Financial Deals Analysis by Type of Cell, 2022 vs 2025
5.5 Cell and Gene Therapy Financial Deals Analysis by Therapeutic Class, 2021 vs 2022
5.6 Cell and Gene Therapy Financial Deals Analysis by Therapeutic Class Prediction, 2022 vs 2025
5.7 Cell and Gene Therapy Financial Deals Analysis by Phase-Wise Deals, 2022 vs 2025
5.8 Cell and Gene Therapy Financial Deals Analysis by Type of Diseases, 2022 vs 2025
5.9 Cell and Gene Therapy Financial Deals Analysis by Type of Industry, 2022 vs 2025
5.10 Cell and Gene Therapy Financial Deals Analysis by Region, 2022 vs 2025
5.11 Cell and Gene Therapy Financial Deals Total Upfront Cash and Equity, 2018-2022
5.12 Number of Cell and Gene Therapy in Clinical Stage, 2018-2022
5.13 Recent Deals and Partnership of Cell and Gene Therapy
5.14 Recent Cell and Gene Therapy Mergers and Acquisitions
5.15 Global Cell and Gene Therapy Deals Landscape, 2020-2022
5.16 Cell and Gene Therapy Financial Deals Analysis by Funding and Investment
Chapter 6 Global Cell and Gene Therapy Patent Analysis & Outlook
6.1 Cell and Gene Therapy Historical and Futuristic Trend of Patent, 2018-2027
6.2 Cell and Gene Therapy Patent Analysis by Type of Cell Therapy Players, 2022 vs 2025
6.3 Cell and Gene Therapy Patent Analysis by Type of Gene Therapy Player, 2022 vs 2025
6.4 Cell and Gene Therapy Patent Analysis by Cell Type, 2022 vs 2025
6.5 Cell and Gene Therapy Patent Analysis by Product
6.6 Cell Therapy Patent Analysis by Patent Type, 2018-2022
6.7 Gene Therapy Patent Analysis by Patent Type, 2018-2022
6.8 Cell Therapy Patent Analysis by Legal Status, 2018-2022
6.9 Gene Therapy Patent Analysis by Legal Status, 2018-2022
6.1 Cell Therapy Patent Analysis by Top Patent Owners
6.11 Gene Therapy Patent Analysis by Top Patent Owners
6.12 Cell Therapy Patent Analysis by Top Patent Applicants
6.13 Gene Therapy Patent Analysis by Top Patent Applicants
6.14 Cell and Gene Therapy: Cell Therapy Top Patent Applicants Benchmarking Analysis
6.15 Cell and Gene Therapy: Gene Therapy Key Patent Applicant Benchmarking Analysis
6.16 Cell Therapy Patent Analysis by Published Status
6.17 Gene Therapy Patent Analysis by Published Status
6.18 Cell Therapy Patent Analysis by Investors
6.19 Gene Therapy Patent Analysis by Investors
6.20 Cell Patent Analysis by CPC Classification Code
6.21 Gene Therapy Patent Analysis by CPC Classification Code
6.22 Cell Therapy Patent Documents by Jurisdiction
6.23 Gene Therapy Patent Documents by Jurisdiction
6.24 List of Recent Cell Therapy Patents
6.25 List of Recent Gene Therapy Patents
Chapter 7 Cell and Gene Therapy Clinical Trial Analysis & Outlook
7.1 Cell and Gene Therapy Clinical Trial Historical and Futuristic Trend
7.2 Cell and Gene Therapy Clinical Trial Region-wise Prediction & Estimation, 2018-2027
7.3 Cell Therapy Clinical Trial Analysis by Country-wise Analysis
7.4 Gene Therapy Clinical Trial Analysis by Country-wise
7.5 Cell and Gene Therapy Clinical Trial Analysis by Age Group
7.6 Cell and Gene Therapy Clinical Trial Analysis by Funding Agency
7.7 Cell and Gene Therapy Clinical Trial Analysis by Documents
7.8 Cell and Gene Therapy Clinical Trial Analysis by Therapeutic Class
7.9 Cell and Gene Therapy Clinical Trial Analysis by Phase-wise
7.10 Cell and Gene Therapy Clinical Trial Analysis by Status
7.11 Number of Cell and Gene Therapy Assets in Clinical Pipeline
7.12 Cell and Gene Therapy Clinical Trial Analysis by Type of Diseases
7.13 Cell and Gene Therapy Clinical Trial Analysis by Study Type
Chapter 8 Cell and Gene Therapy Competitive Landscape Analysis: Key Company Profiles and Strategic Initiatives
8.1 Cell and Gene Therapy Competitive Index Ranking & Attractiveness Quadrant
8.2 Cell and Gene Therapy Company Market Share
8.3 Cell and Gene Therapy Competitive Mapping Quadrant
8.4 Cell and Gene Therapy Competitive Landscape by End Markets
8.5 Key Companies by Regions
8.6 Competitive Landscape by Different Therapy Segment of Cell and Gene Therapy
8.7 Gene Therapy Public Company Competitive Landscape
8.8 Cell Therapy Public Company Competitive Landscape
8.9 Cell and Gene Therapy Developers Worldwide
8.10 Gilead Sciences
8.11 Novartis
8.12 Johnson & Johnson
8.13 Bristol Myers Squibb
8.14 Roche Holding AG
8.15 bluebird bio
8.16 Alnylam Pharmaceuticals
Chapter 9 Global Cell and Gene Therapy Market Size and Forecast, 2018-2027
9.1 Cell and Gene Therapy Market Share by Different Therapy Segment, 2018-2027
9.1.1 Market Size by Cell and Gene Modified Cell Therapies, 2018-2027
9.1.2 Market Size by Gene Therapy and Genome Therapy, 2018-2027
9.1.3 Cell and Gene Therapy Market Size by DNA & RNA Therapeutics, 2018-2027
9.2 Cell and Gene Therapy Market Share by Purpose of Manufacturing, 2018-2027
9.2.1 Cell and Gene Therapy Market Size by Commercial, 2018-2027
9.2.2 Cell and Gene Therapy Market Size by Clinical, 2018-2027
9.3 Cell and Gene Therapy Market Share by Product, 2018-2027
9.4 Cell and Gene Therapy Market Share by Route of Administration, 2018-2027
9.4.1 Cell and Gene Therapy Market Size by Injectables, 2018-2027
9.4.2 Cell and Gene Therapy Market Size by Topicals, 2018-2027
9.4.3 Cell and Gene Therapy Market Size by Infusions, 2018-2027
9.4.4 Cell and Gene Therapy Market Size by Bioscaffolds, 2018-2027
9.5 Cell and Gene Therapy Market Share by Type of Diseases, 2018-2027
9.5.1 Cell and Gene Therapy Market Size by Rare Diseases, 2018-2027
9.5.2 Cell and Gene Therapy Market Size by Non-Rare Diseases, 2018-2027
9.6 Cell and Gene Therapy Market Share by Type of Cell, 2018-2027
9.6.1 Cell and Gene Therapy Market Size by CAR-T Cell, 2018-2027
9.6.2 Cell and Gene Therapy Market Size by TCR Cell, 2018-2027
9.7 Cell and Gene Therapy Market Share by Therapy, 2018-2027
9.7.1 Cell and Gene Therapy Market Size by T-Cell Therapies, 2018-2027
9.7.2 Cell and Gene Therapy Market Size by NK Cell, 2018-2027
9.7.3 Cell and Gene Therapy Market Size by Dendritic Cell Therapies, 2018-2027
9.7.4 Cell and Gene Therapy Market Size by Stem Cell Therapies, 2018-2027
9.8 Cell and Gene Therapy Market Share by Source of Cell, 2018-2027
9.8.1 Cell and Gene Therapy Market Size by Autologous, 2018-2027
9.8.2 Cell and Gene Therapy Market Size by Allogenic, 2018-2027
9.9 Cell and Gene Therapy Market Share by Delivery Mode, 2018-2027
9.9.1 Cell and Gene Therapy Market Size by In-vivo, 2018-2027
9.9.2 Cell and Gene Therapy Market Size by Ex-vivo, 2018-2027
9.10 Cell and Gene Therapy Market Share by Source of Manufacturing, 2018-2027
9.10.1 Cell and Gene Therapy Market Size by In-House, 2018-2027
9.10.2 Cell and Gene Therapy Market Size by Contract Manufacturing, 2018-2027
9.11 Cell and Gene Therapy Market Share by Therapeutic Class, 2018-2027
9.11.1 Cell and Gene Therapy Market Size by Oncology, 2018-2027
9.11.2 Cell and Gene Therapy Market Size by Neurology, 2018-2027
9.11.3 Cell and Gene Therapy Market Size by Ophthalmology, 2018-2027
9.11.4 Cell and Gene Therapy Market Size by Musculoskeletal, 2018-2027
9.11.5 Cell and Gene Therapy Market Size by Others, 2018-2027
9.12 Cell and Gene Therapy Market Share by Technology, 2018-2027
9.12.1 Cell and Gene Therapy Market Size by Viral Vector Technology, 2018-2027
9.12.2 Cell and Gene Therapy Market Size by Cell Immortalization Technology, 2018-2027
9.12.3 Cell and Gene Therapy Market Size by Genome Editing Technology, 2018-2027
9.12.4 Cell and Gene Therapy Market Size by Others Technologies, 2018-2027
9.13 Cell and Gene Therapy Market Share by End User, 2018-2027
9.13.1 Cell and Gene Therapy Market Size by Pharmaceutical & Biotechnology Companies, 2018-2027
9.13.2 Cell and Gene Therapy Market Size by Academic & Research Institutes, 2018-2027
9.13.3 Cell and Gene Therapy Market Size by Hospital & Clinics, 2018-2027
Chapter 9 - Chapter 38: This section contains chapters providing cell and gene therapy market sizing and forecast for additional 20 countries and 6 regions.

Companies Mentioned

  • Gilead Company
  • Novartis
  • Bristol Myers Squibb
  • bluebird bio
  • Johnson & Johnson
  • Roche Holding AG
  • Alnylam Pharmaceuticals

Methodology

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