T Cell Therapy Market Scope And Analysis

  • Report Code : TIPRE00024331
  • Category : Life Sciences
  • Status : Published
  • No. of Pages : 138
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T Cell Therapy Market Scope and Key Players Analysis by 2030

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T Cell Therapy Market Report Scope

Report Attribute Details
Market size in 2022 US$ 2.75 Billion
Market Size by 2030 US$ 9.04 Billion
Global CAGR (2022 - 2030) 16.0%
Historical Data 2020-2021
Forecast period 2023-2030
Segments Covered By Modality
  • Research and Commercialized
By Therapy Type
  • CAR T-cell Therapy
  • T-cell Receptor-based
By Indication
  • Hematologic Malignancies and Solid Tumors
Regions and Countries Covered North America
  • US
  • Canada
  • Mexico
Europe
  • UK
  • Germany
  • France
  • Russia
  • Italy
  • Rest of Europe
Asia-Pacific
  • China
  • India
  • Japan
  • Australia
  • Rest of Asia-Pacific
South and Central America
  • Brazil
  • Argentina
  • Rest of South and Central America
Middle East and Africa
  • South Africa
  • Saudi Arabia
  • UAE
  • Rest of Middle East and Africa
Market leaders and key company profiles
  • Immunocore Holdings Plc
  • Legend Biotech Corp
  • Janssen Global Services LLC
  • Gilead Sciences Inc
  • Bristol Myers Squibb Co
  • Bluebird Bio Inc
  • Novartis AG
  • JW Cayman Therapeutics Co Ltd
  • Cartesian Therapeutics Inc
  • Competitive Landscape and Key Companies:

    A few of the prominent players operating in the global T cell therapy market are Immunocore Holdings Plc, Legend Biotech Corp, Janssen Global Services LLC, Gilead Sciences Inc, Bristol-Myers Squibb Co, Bluebird Bio Inc, Novartis AG, JW (Cayman) Therapeutics Co Ltd, Cartesian Therapeutics Inc, and Innovent Biologics Inc. These companies focus on new technologies, advancements in existing products, and geographic expansions to meet the growing consumer demand worldwide and increase their product range in specialty portfolios. The companies implementing various inorganic and organic developments in the global T cell Therapy market. Below are few instance:

    • In May 2023, Legend Biotech Corporation announced that a Type II variation application was submitted to the European Medicines Agency (EMA) for CARVYKTI based on data from the CARTITUDE-4 study (NCT04181827), which investigates the treatment of adult patients with relapsed and lenalidomide-refractory multiple myeloma who have received one to three prior lines of therapy.
    • In March 2023, JW Therapeutics, an independent and innovative biotechnology company focusing on developing, manufacturing and commercializing cell immunotherapy products, has initiated the clinical study of Carteyva (relmacabtagene autoleucel injection) for first-line treatment in patients with high-risk large B-cell lymphoma and the first patient infusion.
    • In June 2022, The U.S. Food and Drug Administration (FDA) approved Breyanzi (lisocabtagene maraleucel), a CD19-directed chimeric antigen receptor (CAR) T cell therapy, for the treatment of adult patients with large B-cell lymphoma (LBCL), including diffuse large B-cell lymphoma (DLBCL) not otherwise specified (including DLBCL arising from indolent lymphoma), high-grade B-cell lymphoma, primary mediastinal large B-cell lymphoma, and follicular lymphoma grade 3B.