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 |
Key Regions: UK , Japan , Canada , Germany , Switzerland
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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 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.
Horizon Databook provides a detailed overview of country-level data and insights on the U.S. cell therapy market , including forecasts for subscribers. This country databook contains high-level insights into U.S. cell therapy market from 2018 to 2030, including revenue numbers, major trends, and company profiles.
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