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市場調査レポート
商品コード
1678862
CAR-T細胞療法の世界市場の評価:製品別、用途別、エンドユーザー別、地域別、機会、予測(2018年~2032年)CAR T-cell Therapy Market Assessment, By Product, By Application, By End-user, By Region, Opportunities and Forecast, 2018-2032F |
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CAR-T細胞療法の世界市場の評価:製品別、用途別、エンドユーザー別、地域別、機会、予測(2018年~2032年) |
出版日: 2025年03月13日
発行: Market Xcel - Markets and Data
ページ情報: 英文 225 Pages
納期: 3~5営業日
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世界のCAR-T細胞療法の市場規模は、2024年の43億2,000万米ドルから2032年に242億9,000万米ドルに達すると予測され、予測期間の2025年~2032年にCAGRで24.11%の成長が見込まれます。キメラ抗原受容体(CAR)T細胞療法市場は、世界中で血液がんの有病率が高まり、より信頼性の高い治療法を発見するための活動が拡大していることから、大きな成長を示しています。承認されたCAR-T細胞療法は、白血病、リンパ腫、骨髄腫のような複数の種類の血液がんに対して大きな有効性を示すことから、これらの治療法に対する注目度は大幅に高まっており、市場の成長をさらに後押ししています。
新たなCAR-T細胞療法に対する承認の増加や、臨床試験中の強固な製品パイプラインも、市場の拡大に重要な役割を果たしています。市場参入企業間の市場アクセスと収益性の向上を目的とした提携やパートナーシップは、過去の期間において市場の重要な促進要因であったことが証明されており、予測期間も同様の結果が予測されます。さらに、規制遵守と新治療法の承認プロセスの合理化に向けたメーカーの活動の増加は、この市場に対する投資家の関心の高まりもあり、市場の成長を期待させます。
当レポートでは、世界のCAR-T細胞療法市場について調査分析し、市場規模と予測、市場力学、主要企業の情勢などを提供しています。
Global CAR T-cell therapy market is projected to witness a CAGR of 24.11% during the forecast period 2025-2032, growing from USD 4.32 billion in 2024 to USD 24.29 billion in 2032. The chimeric antigen receptor (CAR) T-cell therapy market is witnessing significant growth due to the growing prevalence of hematological malignancies across the globe and efforts to find more reliable treatments for them. The significant efficacy of approved CAR T-cell therapies against several types of hematological malignancies like leukemia, lymphoma, and myeloma has significantly drawn attention toward these therapies, further fueling the market's growth.
An increasing number of approvals for new CAR T-cell therapies and a robust pipeline of products undergoing clinical trials are also playing a crucial role in the market's expansion. Collaborations and partnerships among the market participants to increase market access and profitability have proven to be a significant driver for the market during the historical period and are expected to generate similar results over the forecast period. Additionally, regulatory compliance and increasing efforts of the manufacturers for streamlining the approval process of new therapies coupled with the increasing interest of investors in this market seem promising for market's growth.
Increasing Prevalence of Cancer Boosts Market Demand
As the number of cases of cancer increases, the requirement for advanced therapeutic solutions for effectively treating and managing the condition is also on the rise. Hematological malignancies such as leukemia and lymphoma require innovative treatment solutions such as CAR T-cell therapies as they have shown significant success rates for such conditions. Thus, healthcare institutes across the globe are increasingly focusing on introducing such therapies for treating cancer patients. For instance, in January 2025, Safdarjung Hospital in Delhi, India used a CAR T-cell therapy procedure on a patient suffering from non-Hodgkin lymphoma. This marks the first time CAR T-cell therapy has been used in a central government hospital in India for treating cancer that failed to respond to conventional treatment methods.
Rising Approvals from Regulatory Bodies Supports Market Expansion
The increase in regulatory approvals is playing a crucial role in the growth of the market by allowing wider patient access, encouraging research and development, and increasing investor confidence. As different regulatory bodies recognize the potential of CAR T-cell therapies, they are focusing on streamlining and fast tracking the approval processes, boosting the commercial adoption of the therapies and positively influencing the market's expansion.
For instance, in May 2024, the Food and Drug Administration provided accelerated approval to Juno Therapeutics, Inc. for Breyanzi (lisocabtagene maraleucel) for adults with refractory or relapsed follicular lymphoma, that have received prior systemic therapy. The application was granted orphan drug designation and priority review by the regulatory body. The safety and efficacy of the therapy were evaluated in TRANSCEND-FL (NCT04245839), in an open-label, single-arm, Phase 2, multicenter trial in adults with refractory or relapsed follicular lymphoma.
Lymphoma Accounts for Significant Share of the Market
Due to the high prevalence of the condition and the effective nature of the therapy for treating the disease, the segment holds a significant share in the market. According to the estimates of the American Cancer Society, non-Hodgkin lymphoma accounts for approximately 4% of the cancer cases in America. In order to combat the growing threat of the condition, various regulatory and governing bodies across the globe are increasingly focusing on providing approval to CAR T-cell therapies for treating lymphoma. For instance, in February 2025, the National Institute for Health and Care Excellence (NICE) granted approval to a CAR T-cell therapy for adults with large B-cell lymphoma. The treatment significantly improves survival outcomes and delays the progression of the disease. Lisocabtagene maraleucel is recommended for patients whose cancer has relapsed or is refractory within the first year of the first-line chemoimmunotherapy.
North America Region Holds Major Market Share
With high investment in research and development activities, technological advancements by key players, and presence of advanced healthcare infrastructure, North American countries, including the United States and Canada, are expected to dominate the market with the highest value share. The supportive government initiatives for managing blood-related diseases are also supporting the growth of the market in the region.
Meanwhile, the Asia-Pacific is expected to witness the highest growth over the forecast period. Countries such as Japan, China, and South Korea are significantly investing in CAR T-cell therapy research. The strong market presence of leading players also supporting the market's expansion in the region. Additionally, different governments in the region are recognizing the potential of the CAR T-cell therapies and are increasingly funding research projects to encourage their development.
Future Market Scenario (2025 - 2032F)
The market is expected to witness significant growth in the coming years due to advancements in clinical research, expanded clinical indications of therapy, and rising cases of cancer across the globe. The American Cancer Society estimates that the number of cases of cancer will reach 35 million globally by 2050. Thus, the reliance on CAR T-cell therapy is anticipated to increase significantly over the forecast period.
Meanwhile, innovations aimed at simplifying the manufacturing process and reducing the costs associated with CAR T-cell therapy are expected to improve their accessibility. To support such innovations, leading healthcare and biotech companies are increasingly focusing on developing collaborations. Companies are also focusing on automating production processes for streamlining and standardizing CAR T-cell therapy manufacturing processes, with the goal of reducing processing time and labor cost.
Additionally, CAR T-cell therapies are being increasingly studies in combination with other therapeutic solutions to improve their durability and effectiveness, especially in the cases where traditional treatment options have failed to yield significant results over the patient population. Thus, propelling the utilization of CAR T-cell therapies and providing lucrative growth opportunities for the market.
Key Players Landscape and Outlook
The leading players of the market are significantly focusing on research and development activities and supporting the market's growth and expansion. The companies are also focusing on securing fundings to advanced CAT T therapy trials. For instance, in February 2025, Hemogenyx Pharmaceuticals LLC secured funding to advance its CAR-T therapy trials, aimed at next-generation treatments for acute myeloid leukemia (AML). CAR-T therapy involves the engineering of a patient's T-cells to destroy cancer cells, potentially a more effective and less toxic treatment than traditional chemotherapy. The funding will be used to fund Phase I clinical trials, which will test the safety and preliminary efficacy of this groundbreaking therapy. This development is a significant achievement for Hemogenyx in its pursuit of improving the prognosis of AML patients, who currently have low survival rates. Hemogenyx expects that CAR-T therapy will have a significant impact on the treatment and survival of AML patients.
Similarly, in February 2025, Anixa Biosciences, Inc. announced that it, along with Moffitt Cancer Center, had dosed the third cohort of patients in their Phase 1 clinical trial of their novel CAR-T therapy for recurrent ovarian cancer. After a 30-day confirmation period has passed, the fourth cohort will start with an increase in dose. Anixa's CAR-T technology is designed to target the follicle-stimulating hormone receptor (FSHR), expressed preferentially on ovarian cells and tumor vasculature. The trial (NCT05316129) investigates safety and efficacy in women with recurrent ovarian cancer who have undergone numerous previous treatments. A new protocol amendment allows eligible patients to receive a second dose and enrollment to include rare ovarian cancer subtypes. Such efforts are expected to bolster the availability of advanced treatment technologies and provide lucrative growth opportunities for the market.
All segments will be provided for all regions and countries covered
Companies mentioned above DO NOT hold any order as per market share and can be changed as per information available during research work.