U.S. Cell Therapy Market Size & Outlook, 2023-2030
The cell therapy market in the United States is expected to reach a projected revenue of US$ 10,342.9 million by 2030. A compound annual growth rate of 21.4% is expected of the United States cell therapy market from 2024 to 2030.
The U.S. cell therapy market generated a revenue of USD 2,662.6 million in 2023 and is expected to reach USD 10,342.9 million by 2030.
The U.S. market is expected to grow at a CAGR of 21.4% from 2024 to 2030.
In terms of segment, autologous therapies was the largest revenue generating therapy type in 2023.
Allogeneic Therapies is the most lucrative therapy type segment registering the fastest growth during the forecast period.
Cell therapy market data book summary
Market revenue in 2023
USD 2,662.6 million
Market revenue in 2030
USD 10,342.9 million
Growth rate
21.4% (CAGR from 2023 to 2030)
Largest segment
Autologous therapies
Fastest growing segment
Allogeneic Therapies
Historical data
2018 - 2022
Base year
2023
Forecast period
2024 - 2030
Quantitative units
Revenue in USD million
Market segmentation
Allogeneic Therapies, Autologous Therapies
Key market players worldwide
Novartis AG ADR, Gilead Sciences Inc, Bristol-Myers Squibb Co, Johnson & Johnson, JCR Pharmaceuticals Co Ltd, JW (Cayman) Therapeutics Co Ltd Ordinary Shares, Atara Biotherapeutics Inc, Medipost, Beiersdorf AG, Nkarta Inc Ordinary Shares
Other key industry trends
In terms of revenue, U.S. accounted for 56.2% of the global cell therapy market in 2023.
Country-wise, U.S. is expected to lead the global market in terms of revenue in 2030.
In North America, U.S. cell therapy market is projected to lead the regional market in terms of revenue in 2030.
Canada is the fastest growing regional market in North America and is projected to reach USD 576.5 million by 2030.
The U.S. Food and Drug Administration (FDA) is the main regulatory body in the country. The U.S. regulatory authorities categorize gene, cell, and tissue-engineered products as advanced therapies. Cellular and tissue-based therapies are regulated by the Center for Biologics Evaluation and Research (CBER), which is a part of the Food and Drug Authority.
Cellular therapy products incorporate cellular immunotherapies and different types of allogeneic & autologous cells for certain therapeutic indications, including adult & embryonic stem cells and hematopoietic stem cells. The CBER considers the Federal Food, Drug, and Cosmetic Act and the Public Health Service for regulating cellular therapy products that are either commercialized or in the pipeline.
Cellular therapies are further classified as regulated under Section 361 and Section 351 according to the Public Health Service Act. Similar to other biological drugs, cellular therapy products under section 351 have to receive premarket approval.
The databook is designed to serve as a comprehensive guide to navigating this sector. The databook focuses on market statistics denoted in the form of revenue and y-o-y growth and CAGR across the globe and regions. A detailed competitive and opportunity analyses related to Cell Therapy Market Outlook will help companies and investors design strategic landscapes.
Autologous Therapies was the largest segment with a revenue share of 90.66% in 2023.
Horizon Databook has segmented the U.S. cell therapy market based on allogeneic therapies, autologous therapies covering the revenue growth of each sub-segment from 2018 to 2030.
The U.S. Food and Drug Administration (FDA) is the main regulatory body in the country. The U.S. regulatory authorities categorize gene, cell, and tissue-engineered products as advanced therapies. Cellular and tissue-based therapies are regulated by the Center for Biologics Evaluation and Research (CBER), which is a part of the Food and Drug Authority.
Cellular therapy products incorporate cellular immunotherapies and different types of allogeneic & autologous cells for certain therapeutic indications, including adult & embryonic stem cells and hematopoietic stem cells. The CBER considers the Federal Food, Drug, and Cosmetic Act and the Public Health Service for regulating cellular therapy products that are either commercialized or in the pipeline.
Cellular therapies are further classified as regulated under Section 361 and Section 351 according to the Public Health Service Act. Similar to other biological drugs, cellular therapy products under section 351 have to receive premarket approval.
U.S. Cell Therapy Market Therapy Type Outlook (Revenue, USD Million , 2018-2030)
Allogeneic Therapies
Autologous Therapies
U.S. Cell Therapy Market Therapeutic Area Outlook (Revenue, USD Million , 2018-2030)
Oncology
Cardiovascular Disease (CVD)
Musculoskeletal Disorders
Dermatology
Others
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Horizon Databook provides a detailed overview of country-level data and insights on the U.S. Cell Therapy Market Outlook, including forecasts for subscribers. This country databook contains high-level insights into U.S. Cell Therapy Market Outlook from 2018 to 2030, including revenue numbers, major trends, and company profiles.