Market revenue in 2021 | USD 1,373.3 million |
Market revenue in 2028 | USD 3,066.7 million |
Growth rate | 12.2% (CAGR from 2021 to 2028) |
Largest segment | Commercialized |
Fastest growing segment | Commercialized |
Historical data covered | 2018 - 2020 |
Base year for estimation | 2021 |
Forecast period covered | 2022 - 2028 |
Quantitative units | Revenue in USD million |
Market segmentation | Research, Commercialized |
Key market players worldwide | Novartis AG ADR, Merck KGaA, Gilead Sciences Inc, Adaptimmune Therapeutics PLC ADR, Bluebird bio Inc, Sorrento Therapeutics Inc, Fate Therapeutics Inc, Pfizer Inc, Amgen Inc, Bristol-Myers Squibb Co |
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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 t-cell therapy market will help companies and investors design strategic landscapes.
Commercialized was the largest segment with a revenue share of 67.1% in 2021. Horizon Databook has segmented the Europe t-cell therapy market based on research, commercialized covering the revenue growth of each sub-segment from 2018 to 2028.
The European region is expected to follow closely behind the North American region in terms of revenue share. Post assessment by the UK’s National Institute for Health and Care Excellence, T-cell therapies, Yescarta and Kymriah, were approved by the EU in the year 2018. According to European Hematology Association in 2019, approximately 340 patients were treated with T-cell therapies in the European region, with a majority being treated during clinical trial evaluations.
It was also reported that in addition to the approved indications—B-cell lymphoma and B-cell ALL—the use of these therapies is being extended to other hematological diseases such as multiple myeloma, acute myeloid leukemia, and Hodgkin lymphoma.
In 2018, the European Medicines Agency (EMA) recommended marketing authorization for Kymriah and Yescarta, boosting adoption of T-cell therapies in the region. The therapies were the first to be approved through EMA Priority Medicines (PRIME) program, which has been specifically designed for the approval of innovative drug therapies.
Horizon Databook provides a detailed overview of continent-level data and insights on the Europe t-cell therapy market , including forecasts for subscribers. This continent databook contains high-level insights into Europe t-cell therapy market from 2018 to 2028, including revenue numbers, major trends, and company profiles.
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