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Chimeric Antigen Receptor T-Cell Therapy (CAR-T) Pipeline Analysis Report 2025

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    Report

  • 200 Pages
  • June 2025
  • Region: Global
  • Expert Market Research
  • ID: 6102837
Chimeric antigen receptor T-cell therapy (CAR-T) is an innovative cancer treatment that modifies a patient's T-cells to recognize and attack cancer cells. The therapy addresses the high unmet clinical need for more effective treatments, particularly for diseases such as lymphoma and leukemia, where current options like chemotherapy and stem cell transplants often fall short. The growing focus on personalized medicine and immune oncology is driving the expansion of CAR-T therapies. In September 2024, the European Society for Blood and Marrow Transplantation (EBMT) reached a milestone of 10,000 CAR-T patients, highlighting its growing significance. Continued focus on improving efficacy and expanding indications is expected to drive further pipeline development and innovation in this field.

Report Coverage

The Chimeric Antigen Receptor T-Cell Therapy (CAR-T) Drug Pipeline Insight Report by the publisher gives comprehensive insights into chimeric antigen receptor T-cell therapy (CAR-T) therapeutics currently undergoing clinical trials. It covers various aspects related to the details of each of these drugs under development for chimeric antigen receptor T-cell therapy (CAR-T). The chimeric antigen receptor T-cell therapy (CAR-T) report assessment includes the analysis of over 100 pipeline drugs and 50+ companies. The chimeric antigen receptor T-cell therapy (CAR-T) pipeline landscape will include an analysis based on efficacy and safety measure outcomes published for the trials, including their adverse effects on patients suffering from the condition, and alignment with chimeric antigen receptor T-cell therapy (CAR-T) treatment guidelines to ensure optimal care practices.

The assessment part will include a detailed analysis of each drug, drug class, clinical studies, phase type, drug type, route of administration, and ongoing product development activities related to chimeric antigen receptor T-cell therapy (CAR-T).

Chimeric Antigen Receptor T-Cell Therapy (CAR-T) Drug Pipeline Outlook

Chimeric antigen receptor T-cell therapy (CAR-T) is a groundbreaking immunotherapy that modifies a patient's T-cells to express a receptor specific to cancer cells. The modified T-cells are then reintroduced into the body to target and destroy malignant cells. This treatment is particularly effective in hematological cancers, such as leukemia and lymphoma, and has shown promise in other malignancies.

Chimeric antigen receptor T-cell therapy (CAR-T) is primarily used in the treatment of leukemia and lymphoma, including B-cell acute lymphoblastic leukemia (ALL), chronic lymphocytic leukemia (CLL), and diffuse large B-cell lymphoma (DLBCL). These cancers, often resistant to conventional therapies like chemotherapy, have seen remarkable responses to CAR-T, offering hope to patients who previously had limited treatment options.

Chimeric Antigen Receptor T-Cell Therapy (CAR-T) - Drug Pipeline Therapeutic Assessment

This section of the report covers the analysis of chimeric antigen receptor T-cell therapy (CAR-T) drug candidates based on several segmentations, including:

By Phase

  • Late-Stage Products (Phase 3 and Phase 4)
  • Mid-Stage Products (Phase 2)
  • Early-Stage Products (Phase I)
  • Preclinical and Discovery Stage Products

By Drug Class

  • Small Molecules
  • Monoclonal Antibodies
  • Gene Therapies
  • Others

By Route of Administration

  • Oral
  • Parenteral
  • Others

Chimeric Antigen Receptor T-Cell Therapy (CAR-T) Pipeline Assessment Segmentation, By Phases

The report covers phase I, phase II, phase III, phase IV, and early-phase drugs. The coverage includes an in-depth analysis of each drug across these phases. According to analysis, phase I covers a major share of the total chimeric antigen receptor T-cell therapy (CAR-T) clinical trials.

Chimeric Antigen Receptor T-Cell Therapy (CAR-T) Pipeline Assessment Segmentation, By Drug Classes

The drug molecule categories covered under the chimeric antigen receptor T-cell therapy (CAR-T) pipeline analysis include small molecules, monoclonal antibodies, and gene therapies. The report provides a comparative analysis of the drug classes for each drug in various phases of clinical trials for chimeric antigen receptor T-cell therapy (CAR-T).

Chimeric Antigen Receptor T-Cell Therapy (CAR-T) Clinical Trials Therapeutic Assessment - Competitive Dynamics

The report for the chimeric antigen receptor T-cell therapy (CAR-T) report insights includes the profile of key companies involved in clinical trials and their drugs under development. Below is the list of a few players involved in chimeric antigen receptor T-cell therapy (CAR-T) clinical trials:
  • Novartis Pharmaceuticals
  • Wugen, Inc.
  • Caribou Biosciences, Inc.
  • Tcelltech Inc.
  • Shanghai Ming Ju Biotechnology Co., Ltd.
  • PersonGen BioTherapeutics (Suzhou) Co., Ltd.
  • Suzhou Immunofoco Biotechnology Co., Ltd.
  • Arcellx, Inc.
  • Bristol-Myers Squibb
  • Genentech, Inc.

Chimeric Antigen Receptor T-Cell Therapy (CAR-T) Emerging Drugs Profile

This section covers the detailed analysis of each drug under multiple phases, including phase I, phase II, phase III, phase IV, and emerging drugs for chimeric antigen receptor T-cell therapy (CAR-T). It includes product description, trial ID, study type, drug class, mode of administration, and recruitment status of chimeric antigen receptor T-cell therapy (CAR-T) drug candidates.

Drug: Clarithromycin, Lenalidomide, Dexamethasone and Autologous BCMA-directed CAR T-Cells

The CARTITUDE-5 study, sponsored by Janssen Research & Development, LLC, is evaluating the efficacy of Bortezomib, Lenalidomide, and Dexamethasone (VRd) followed by a single dose of Ciltacabtagene Autoleucel (cilta-cel), a CAR-T therapy targeting BCMA, compared to VRd followed by Lenalidomide and Dexamethasone (Rd) in newly diagnosed multiple myeloma patients. The study, enrolling 743 participants, is expected to be completed by December 2034.

Genetic: GLPG CAR T-cell therapy

The long-term follow-up study of participants treated with Galapagos Chimeric Antigen Receptor (CAR) T-cell therapies (known as Hesperia) is being sponsored by Galapagos NV. The objective of this Phase 3 study is to evaluate the long-term safety and efficacy of GLPG CAR T-cell therapies for up to 15 years post-infusion. The study, expected to be complete by July 2039, involves 546 participants.

Reasons To Buy This Report

The Chimeric Antigen Receptor T-Cell Therapy (CAR-T) Drug Pipeline Insight Report provides a strategic overview of the latest and future landscape of treatments for chimeric antigen receptor T-cell therapy (CAR-T). It provides necessary information for making informed investment decisions along with research, development, and strategic planning efforts. The stakeholders will benefit from the essential insights into market trends, regulatory environments, and potential growth opportunities within chimeric antigen receptor T-cell therapy (CAR-T) pipeline insights.

Key Questions Answered in the Chimeric Antigen Receptor T-Cell Therapy (CAR-T) Pipeline Insight Report

  • Which companies/institutions are leading the chimeric antigen receptor T-cell therapy (CAR-T) drug development?
  • What is the efficacy and safety profile of chimeric antigen receptor T-cell therapy (CAR-T) pipeline drugs?
  • Which company is leading the chimeric antigen receptor T-cell therapy (CAR-T) pipeline development activities?
  • What is the current chimeric antigen receptor T-cell therapy (CAR-T) commercial assessment?
  • What are the opportunities and challenges present in the chimeric antigen receptor T-cell therapy (CAR-T) drug pipeline landscape?
  • What is the efficacy and safety profile of chimeric antigen receptor T-cell therapy (CAR-T) pipeline drugs?
  • Which company is conducting major trials for chimeric antigen receptor T-cell therapy (CAR-T) drugs?
  • Which companies/institutions are involved in chimeric antigen receptor T-cell therapy (CAR-T) collaborations aimed at providing enhanced therapeutic alternatives for patients?
  • What are the geographies covered for clinical trials in chimeric antigen receptor T-cell therapy (CAR-T)?

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Table of Contents

1 Preface
1.1 Introduction
1.2 Objectives of the Study
1.3 Research Methodology & Assumptions
2 Executive Summary
3 Overview of Chimeric Antigen Receptor T-Cell Therapy (CAR-T)
3.1 Signs and Symptoms
3.2 Causes
3.3 Risk Factors
3.4 Diagnosis
3.5 Treatment
4 Patient Profile: Chimeric Antigen Receptor T-Cell Therapy (CAR-T)
4.1 Patient Profile Overview
4.2 Patient Psychology and Emotional Impact Factors
4.3 Risk Assessment and Treatment Success Rate
5 Chimeric Antigen Receptor T-Cell Therapy (CAR-T): Epidemiology Snapshot
5.1 Chimeric Antigen Receptor T-Cell Therapy (CAR-T) Incidence by Key Markets
5.2 Chimeric Antigen Receptor T-Cell Therapy (CAR-T) - Patients Seeking Treatment in Key Markets
6 Chimeric Antigen Receptor T-Cell Therapy (CAR-T): Market Dynamics
6.1 Market Drivers and Constraints
6.2 SWOT Analysis
7 Chimeric Antigen Receptor T-Cell Therapy (CAR-T): Key Facts Covered
7.1 Top Countries Contributing to Clinical Trials in Asia-Pacific
7.2 Top Countries Contributing to Clinical Trials in Europe
7.3 Top Countries Contributing to Clinical Trials in North America
7.4 Top Countries Contributing to Clinical Trials in Other Regions
8 Chimeric Antigen Receptor T-Cell Therapy (CAR-T), Drug Pipeline Assessment
8.1 Assessment by Treatment Type
8.2 Assessment by Route of Administration
8.3 Assessment by Drug Class
9 Drug Pipeline Comparative Analysis
9.1 List of Chimeric Antigen Receptor T-Cell Therapy (CAR-T) Pipeline Drugs
9.1.1 By Company
9.1.2 By Phase
9.1.3 By Indication
9.1.4 By Trial Status
9.1.5 By Funder Type
9.2 Attribute Scoring Analysis of Pipeline Drugs (Top Drugs)
10 Chimeric Antigen Receptor T-Cell Therapy (CAR-T) Drug Pipeline - Late-Stage Products (Phase III and IV) (Top Drugs)
10.1 Comparative Analysis for Late-Stage Drugs
10.1.1 Study Type
10.1.2 Recruitment Status
10.1.3 Company
10.1.4 Funder Type
10.2 Product Level Analysis*
10.2.1 Genetic: GLPG CAR T-cell therapy
10.2.1.1 Product Description
10.2.1.2 Trial ID
10.2.1.3 Sponsor Name
10.2.1.4 Study Type
10.2.1.5 Drug Class
10.2.1.6 Eligibility Criteria
10.2.1.7 Study Record Dates
10.2.1.7.1 First Submitted
10.2.1.7.2 First Posted
10.2.1.7.3 Last Update Posted
10.2.1.7.4 Last Verified
10.2.1.8 Indication
10.2.1.9 Study Design
10.2.1.10 Recruitment Status
10.2.1.11 Enrollment (Estimated)
10.2.1.12 Location Countries
10.2.1.13 Recent Results
10.2.2 Drug: Clarithromycin, Lenalidomide, Dexamethasone and Autologous BCMA-directed CAR T-Cells
10.2.3 Other Drugs
11 Chimeric Antigen Receptor T-Cell Therapy (CAR-T) Drug Pipeline - Mid-Stage Products (Phase II) (Top Drugs)
11.1 Comparative Analysis for Mid-Stage Drugs
11.1.1 Study Type
11.1.2 Recruitment Status
11.1.3 Company
11.1.4 Funder Type
11.2 Product Level Analysis*
11.2.1 Drug: Itacitinib
11.2.1.1 Product Description
11.2.1.2 Trial ID
11.2.1.3 Sponsor Name
11.2.1.4 Study Type
11.2.1.5 Drug Class
11.2.1.6 Eligibility Criteria
11.2.1.7 Study Record Dates
11.2.1.7.1 First Submitted
11.2.1.7.2 First Posted
11.2.1.7.3 Last Update Posted
11.2.1.7.4 Last Verified
11.2.1.8 Indication
11.2.1.9 Study Design
11.2.1.10 Recruitment Status
11.2.1.11 Enrollment (Estimated)
11.2.1.12 Location Countries
11.2.1.13 Recent Results
11.2.2 Biological: LCAR-B38M CAR-T Cell
11.2.3 Drug: Mosunetuzumab, Polatuzumab
11.2.4 Other Drugs
12 Chimeric Antigen Receptor T-Cell Therapy (CAR-T) Drug Pipeline - Early-Stage Products (Phase I) (Top Drugs)
12.1 Comparative Analysis for Early-Stage Drugs
12.1.1 Study Type
12.1.2 Recruitment Status
12.1.3 Company
12.1.4 Funder Type
12.2 Product Level Analysis*
12.2.1 Biological: iC9-CAR.B7-H3 T Cell Therapy, Drug: cyclophosphamide, fludarabine
12.2.1.1 Product Description
12.2.1.2 Trial ID
12.2.1.3 Sponsor Name
12.2.1.4 Study Type
12.2.1.5 Drug Class
12.2.1.6 Eligibility Criteria
12.2.1.7 Study Record Dates
12.2.1.7.1 First Submitted
12.2.1.7.2 First Posted
12.2.1.7.3 Last Update Posted
12.2.1.7.4 Last Verified
12.2.1.8 Indication
12.2.1.9 Study Design
12.2.1.10 Recruitment Status
12.2.1.11 Enrollment (Estimated)
12.2.1.12 Location Countries
12.2.2 Biological: WZTL002-1 (1928T2z CAR-T cells), Drug: Cyclophosphamide and Fludarabine lymphodepleting chemotherapy
12.2.3 Drug: Duvelisib
12.2.4 Other Drugs
13 Chimeric Antigen Receptor T-Cell Therapy (CAR-T) Drug Pipeline - Preclinical and Discovery Stage Products (Top Drugs)
13.1 Comparative Analysis for Preclinical and Discovery Stage Drugs
13.1.1 Study Type
13.1.2 Recruitment Status
13.1.3 Company
13.1.4 Funder Type
13.2 Product Level Analysis*
13.2.1 Drug: CD19/CD20/BCMA CAR-T
13.2.1.1 Product Description
13.2.1.2 Trial ID
13.2.1.3 Sponsor Name
13.2.1.4 Study Type
13.2.1.5 Drug Class
13.2.1.6 Eligibility Criteria
13.2.1.7 Study Record Dates
13.2.1.7.1 First Submitted
13.2.1.7.2 First Posted
13.2.1.7.3 Last Update Posted
13.2.1.7.4 Last Verified
13.2.1.8 Indication
13.2.1.9 Study Design
13.2.1.10 Recruitment Status
13.2.1.11 Enrollment (Estimated)
13.2.1.12 Location Countries
13.2.2 Biological: CD19/CD20/BCMA CAR T cells
13.2.3 Other Drugs
14 Chimeric Antigen Receptor T-Cell Therapy (CAR-T), Key Drug Pipeline Companies
14.1 Novartis Pharmaceuticals
14.1.1 Company Snapshot
14.1.2 Pipeline Product Portfolio
14.1.3 Financial Analysis
14.1.4 Recent News and Developments
14.2 Wugen, Inc.
14.2.1 Company Snapshot
14.2.2 Pipeline Product Portfolio
14.2.3 Financial Analysis
14.2.4 Recent News and Developments
14.3 Caribou Biosciences, Inc.
14.3.1 Company Snapshot
14.3.2 Pipeline Product Portfolio
14.3.3 Financial Analysis
14.3.4 Recent News and Developments
14.4 Tcelltech Inc.
14.4.1 Company Snapshot
14.4.2 Pipeline Product Portfolio
14.4.3 Financial Analysis
14.4.4 Recent News and Developments
14.5 Shanghai Ming Ju Biotechnology Co., Ltd.
14.5.1 Company Snapshot
14.5.2 Pipeline Product Portfolio
14.5.3 Financial Analysis
14.5.4 Recent News and Developments
14.6 PersonGen BioTherapeutics (Suzhou) Co., Ltd.
14.6.1 Company Snapshot
14.6.2 Pipeline Product Portfolio
14.6.3 Financial Analysis
14.6.4 Recent News and Developments
14.7 Suzhou Immunofoco Biotechnology Co., Ltd.
14.7.1 Company Snapshot
14.7.2 Pipeline Product Portfolio
14.7.3 Financial Analysis
14.7.4 Recent News and Developments
14.8 Arcellx, Inc.
14.8.1 Company Snapshot
14.8.2 Pipeline Product Portfolio
14.8.3 Financial Analysis
14.8.4 Recent News and Developments
14.9 Bristol-Myers Squibb
14.9.1 Company Snapshot
14.9.2 Pipeline Product Portfolio
14.9.3 Financial Analysis
14.9.4 Recent News and Developments
14.10 Genentech, Inc.
14.10.1 Company Snapshot
14.10.2 Pipeline Product Portfolio
14.10.3 Financial Analysis
14.10.4 Recent News and Developments
15 Regulatory Framework for Drug Approval, By Region16 Terminated or Suspended Pipeline Products