Global CAR T-cell Therapy Market Assessment, By Product [Yescarta (axicabtagene ciloleucel), Kymriah (tisagenlecleucel), Abecma (idecabtagene vicleucel), Tecartus (brexucabtagene autoleucel), Breyanzi (lisocabtagene maraleucel), Others], By Application [Leukemia, Lymphoma, Multiple Myeloma, Others], By End-user [Hospitals, Cancer Care Treatment Centers], By Region, Opportunities and Forecast, 2018-2032F

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. 

CAR T-cell Therapy Market Size, Share, Growth & Demand Forecast 2032

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&rsquo;s growth.
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Details
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Base Year of the Analysis
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2024
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Historical Period
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2018-2023
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Forecast Period
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2025-2032
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Projected Growth Rate
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CAGR of 24.11% between 2025 and 2032
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Revenue Forecast in 2032
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USD 24.29 billion
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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&rsquo;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&rsquo;s growth.
<h2>Increasing Prevalence of Cancer Boosts Market Demand</h2>
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.
<h2>Rising Approvals from Regulatory Bodies Supports Market Expansion</h2>
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&rsquo;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.
<h2>Lymphoma&nbsp;Accounts for Significant Share of the Market</h2>
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&rsquo;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.
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Future Market Scenario (2025 &ndash; 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.&nbsp; 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.
Report Scope
&ldquo;CAR T-cell Therapy&nbsp;Market Assessment, Opportunities and Forecast, 2018-2032F&rdquo;,&nbsp;is a comprehensive report by Markets and Data, providing in-depth analysis and qualitative and quantitative assessment of the current state of global CAR T-cell therapy market, industry dynamics, and challenges. The report includes market size, segmental shares, growth trends, opportunities, and forecast between 2025 and 2032. Additionally, the report profiles the leading players in the industry, mentioning their respective market share, business models, competitive intelligence, etc.
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Details
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Segments Covered
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Product, Application, End-user
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Regions Covered
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North America, Europe, South America, Asia-Pacific, Middle East and Africa
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Key Companies Profile
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Gilead Sciences, Inc., Janssen Biotech, Inc., Novartis Pharmaceutical Corporation, Bristol-Myers Squibb Company, JW Therapeutics (Shanghai) Co., Ltd., Bluebird bio, Inc., Merck &amp; Co., Inc., Johnson &amp; Johnson Services, Inc., Sorrento Therapeutics, Inc., Sangamo Therapeutics, Inc.
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Customization Scope
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15% free report customization with purchase
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Pricing and Purchase Options
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Avail the customized purchase options to fulfill your precise research needs
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Delivery Format
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PDF and Excel through email (subject to the license purchased)
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In the report,&nbsp;global&nbsp;CAR T-cell therapy&nbsp;market&nbsp;has been segmented into the following categories:&nbsp;
<ul>
<li>By Product
<ul>
<li>Yescarta&nbsp;(axicabtagene ciloleucel)</li>
<li>Kymriah&nbsp;(tisagenlecleucel)</li>
<li>Abecma&nbsp;(idecabtagene vicleucel)</li>
<li>Tecartus&nbsp;(brexucabtagene autoleucel)</li>
<li>Breyanzi&nbsp;(lisocabtagene maraleucel)</li>
<li>Others</li>
</ul>
</li>
<li>By Application
<ul>
<li>Leukemia</li>
<li>Lymphoma</li>
<li>Multiple Myeloma</li>
<li>Others</li>
</ul>
</li>
<li>By End-user
<ul>
<li>Hospitals</li>
<li>Cancer Care Treatment Centers</li>
</ul>
</li>
<li>By Region
<ul>
<li>North America</li>
<li>Europe</li>
<li>Asia-Pacific</li>
<li>South America</li>
<li>Middle East and Africa</li>
</ul>
</li>
</ul>
Key Players Landscape and Outlook
The leading players of the market are significantly focusing on research and development activities and supporting the market&rsquo;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.
Key Players Operating in Global&nbsp;CAR T-cell Therapy&nbsp;Market are:
<ul>
<li>Gilead Sciences, Inc.</li>
<li>Janssen Biotech, Inc.</li>
<li>Novartis Pharmaceutical Corporation</li>
<li>Bristol-Myers Squibb Company</li>
<li>JW Therapeutics (Shanghai) Co., Ltd.</li>
<li>Bluebird bio, Inc.</li>
<li>Merck &amp; Co., Inc.</li>
<li>Johnson &amp; Johnson Services, Inc.</li>
<li>Sorrento Therapeutics, Inc.</li>
<li>Sangamo Therapeutics, Inc.</li>
</ul>
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Global CAR T-cell Therapy Market Assessment, Opportunities and Forecast, 2018-2032F

The market is expected to witness significant growth in the coming years due to rising prevalence on cancer in different regions, increasing investments in development of new therapies, and growing focus on streamlining approval processes for CAR T-cell therapies.

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