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Vertical Industries Immune Cell Therapy

Immune Cell Therapy

01
China's Immune Cell Therapy Sector Faces Rapid Growth Opportunities

As the world's second-largest pharmaceutical market, China has accelerated its catch-up in the field of immune cell therapy in recent years. Policy dividends, technological breakthroughs and surging capital inflows have jointly propelled the industry into a fast growth track. The sector is expected to enter a period of rapid expansion from 2026 to 2030, with its market size projected to exceed 20 billion yuan.

02
Specialized Survey of Nearly 200 Enterprises
VCBeat conducted a specialized survey of nearly 200 domestic relevant enterprises. It screened enterprises from multiple dimensions such as financing capacity, R&D product pipelines, cross-border cooperation and core teams. In addition, it divided nine mainstream segmented tracks according to drug mechanisms of action and built a complete industrial map for immune cell therapy.
03
Multi-dimensional Industrial Map of Immune Cell Therapy
This map clearly presents the enterprise count and core technological directions across the nine mainstream tracks. It also compiles basic profiles of nearly 200 companies, including establishment dates, business locations, employee size, contact information, official websites, financing records and latest corporate developments.
04
Full-spectrum Data Support & Collaboration
VCBeat has built in-depth connections with all enterprises on the map, offering exclusive cooperation channels and providing full-spectrum, authoritative data to support industrial planning, trend analysis, business collaboration and investment decision-making.

Industry Map

CAR-T (79)
Chimeric antigen receptor T-cell therapy.
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TCR-T (23)
T cell receptor-engineered T cell therapy.
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NK、CAR-NK (34)
Natural killer cell therapy, chimeric antigen receptor natural killer cell therapy.
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CAR-NKT (5)
Chimeric antigen receptor natural killer T cell therapy.
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CAR-M (4)
Chimeric antigen receptor macrophage therapy.
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CAR-γδ T (6)
Chimeric antigen receptor γδ T cells.
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TIL (14)
Tumor-infiltrating lymphocyte therapy.
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Treg (4)
Regulatory T-cell therapy.
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DC、CIK、DC-CIK (10)
Dendritic cell immunotherapy, cytokine-induced killer cell therapy, dendritic cell-cytokine induced killer cell therapy.
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Others (6)
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Finance

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Time
Company Name
Brief Introduction
Area
Funding rounds
Amount
June 17, 2026
Developer of Tumor Cell Immunotherapy Technologies and Products
Jiangsu,China
Series C+
Undisclosed
June 12, 2026
Developer of Next-Generation Anti-Tumor DNA Vaccines
Beijing,China
Series B
CNY 100M
June 09, 2026
Developer of γδ T Cell Therapeutics
Beijing,China
Series A
Nearly CNY 200M
June 09, 2026
Developer of Tumor Immune Cell Therapy Technologies and Products
Shanghai,China
-
Undisclosed
Time
Company Name
Brief Introduction
Area
Funding rounds
Amount
December 30, 2022
Integrated Biopharmaceutical R&D and Manufacturing Company
Shandong,China
IPO
HKD 152.8M
December 15, 2021
Developer of Molecular Targeted and Immune Anti-Tumor Drugs
Beijing,China
IPO
CNY 22.2B
June 18, 2021
Developer of CAR-T Cell Immunotherapy Drugs
Shanghai,China
IPO
HKD 2.94B
January 09, 2021
Cell and Gene Therapy Developer
Shanghai,China
IPO
USD 240M
November 03, 2020
Developer of Cellular Immunotherapy Products
Shanghai,China
IPO
HKD 10B
July 10, 2020
Developer of Cellular Immunotherapy Products
Beijing,China
IPO
HKD 1.0241B
June 05, 2020
Tumor Cell Immunotherapy Developer
Jiangsu,China
IPO
USD 424M
October 31, 2018
High-end Biologics Developer
Jiangsu,China
IPO
HKD 3.2B
August 08, 2018
Developer of Molecular Targeted and Immune Anti-Tumor Drugs
Beijing,China
IPO
HKD 7.085B
October 28, 2016
Pharmaceutical Circulation Service Provider
Beijing,China
IPO
HKD 13.97B

Business Development

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Transaction Type
Transaction Date
Transferor (Seller)
Transferee (Buyer)
Trading products
Clinical Stage
Amount
Source
license in
2026-06-30
Verzenio®
NMPA Approval for Market Launch
Undisclosed
license out
2026-06-11
--
BA5101
NMPA Approval for Market Launch
Undisclosed
license out
2026-05-29
12 Innovative Drug Projects for Early-Stage Tumors
Preclinical R&D Phase
USD 10.5B
cooperative development
2026-05-27
Antaisi ®
NMPA Approved for Marketing
Undisclosed
cooperative development
2026-05-21
Targeted LNP Delivery Technology
Preclinical R&D Phase
Undisclosed
license out
2026-04-10
CAR-T Cell Therapy
--
Undisclosed
cooperative development
2026-03-05
Antibody drugs, Antibody-Drug Conjugates (ADC), T-cell Engagers (TCE)
--
Undisclosed
license out
2026-02-08
Innovative Drugs in Oncology and Immunology
--
USD 8.85B
license out
2026-01-15
BZDS1901
--
Undisclosed
license in
2026-01-14
ElpasBio Holdings
AlloJoin®(lotazadromcel)
--
Undisclosed

Industry Insights

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Innovation
Imunopharm Technology Files for STAR Market IPO, Seeking to Raise 2.5 Billion Yuan for Cell Therapy Pipeline
Imunopharm Technology Co., Ltd., a Chinese biotech specializing in gene and cell therapies, has filed for an IPO on the Shanghai Stock Exchange's STAR Market to raise 2.5 billion yuan ($345 million). The funds will support R&D, manufacturing, and working capital. Founded in 2015 by a Tsinghua University team, the company has developed core platforms for gene delivery and immune cell therapies. Its flagship product, IM19, a CD19-targeting CAR-T therapy for non-Hodgkin lymphoma, has submitted an NDA and secured commercialization rights with Huadong Medicine. The pipeline extends to solid tumors with IM96 (globally approved for colorectal cancer trials), autoimmune diseases with ZM001, and next-gen technologies like in vivo CAR-T. Despite operating at a loss, the company aims to leverage its innovative platforms and diverse pipeline to compete in China's growing CAR-T market.
4min read
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Innovation
BeOne Medicines Announces Positive Phase 3 MANGROVE Trial Results for Zanubrutinib in First-Line Mantle Cell Lymphoma
BeOne Medicines announced that its Phase 3 MANGROVE trial met its primary endpoint, demonstrating that a chemotherapy-free regimen of zanubrutinib plus rituximab significantly reduced the risk of disease progression or death by 43% compared to standard bendamustine-rituximab in previously untreated mantle cell lymphoma patients (HR=0.57). This marks the first Phase 3 trial evaluating a chemotherapy-free, BTK inhibitor-based regimen in the first-line setting, offering a highly effective alternative that spares patients, particularly the elderly, from the cumulative toxicities and infusion burden of traditional chemotherapy. The company plans to present full results at an upcoming medical conference and expects to file for regulatory approvals in the second half of 2026.
3min read
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Innovation
5th Anniversary of Yescarta® Launch: The Milestone Journey of China's CAR-T Therapy from Zero to One
In June 2026, Yescarta® (axicabtagene ciloleucel), the flagship CAR-T therapy from Shanghai Fosun Kairos Biotechnology, celebrates its fifth anniversary as China's first approved cell therapy product. Approved by the NMPA on June 22, 2021, Yescarta® broke the zero-to-one barrier in domestic cell treatment and has since treated over 1,500 patients with relapsed or refractory lymphoma. Key milestones include China's first CAR-T patient achieving over eight years of cancer-free survival, the approval of a second indication for adult large B-cell lymphoma in June 2023, and the establishment of a national treatment network spanning more than 200 high-standard treatment centers across 29 provinces. The company's third indication filing for indolent non-Hodgkin lymphoma has received Breakthrough Therapy Designation. Looking forward, Fosun Kairos plans to expand its pipeline into solid tumors, autoimmune diseases, and frontier technologies including in-vivo CAR-T and CAR-NK therapies, solidifying its position as a leader in China's cell and gene therapy field.
2min read
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Innovation
China's First TIL Therapy GT101 Granted IND for First-Line Treatment of Head and Neck Squamous Cell Carcinoma
Beijing Grit Biotherapeutics has received IND approval from China's NMPA for GT101, a tumor-infiltrating lymphocyte (TIL) therapy, for the first-line treatment of recurrent or metastatic head and neck squamous cell carcinoma. This marks China's first approved clinical trial for a TIL therapy in this indication. GT101 has previously demonstrated promising efficacy in cervical cancer, achieving a 45.5% objective response rate and complete remission in a patient, as presented at the ASCO annual meeting. Grit Biotherapeutics continues to expand its pipeline of innovative cellular therapies targeting solid tumors.
2min read
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In DepthInnovation
Three World-First Therapies Approved on the Same Day: How to Navigate Commercialization After Solid Tumor CAR-T Is Priced at 990,000 RMB
Data from a confirmatory Phase II randomized controlled trial in China showed that, among treated patients, the median progression-free survival (PFS) was 4.37 months in the Kailimei® group versus 1.84 months in the control group, representing a nearly 70% reduction in the risk of disease progression or death. In terms of median overall survival (OS), the Kailimei group achieved 9.49 months, compared with 5.49 months in the control group.
6min read
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In DepthMNC China Lens
$28.7 Billion in Three Licensing Deals: Chinese Pharma Rewrites the Playbook
The innovative drug industry is fiercely competitive, with a scarcity of high-quality, differentiated late-stage pipelines, forcing MNCs to pivot toward early-stage projects. Although China's innovative drug R&D system is characterized by being "fast, cost-effective, and efficient," this does not alter the fundamental principles of drug development: late-stage projects have a higher likelihood of successful commercialization, whereas early-stage projects suffer from lower success rates.
8min read
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Innovation
BeOne Medicines Unveils Breakthrough Hematology Data at EHA 2026, Redefining B-Cell Malignancy Treatment
At the 2026 European Hematology Association (EHA) Annual Congress in Stockholm, BeOne Medicines presented pivotal data highlighting its leadership in B-cell malignancy treatment. The oral BTK protein degrader tacabrutideg (BGB-16673) demonstrated an 85.1% overall response rate (ORR) in heavily pretreated relapsed/refractory (R/R) CLL/SLL patients, including those with high-risk features, and showed early efficacy in BTK inhibitor-naïve patients. Meanwhile, the all-oral zanubrutinib + sotorasibrant (ZS) combination achieved a 100% ORR and 98.8% uMRD4 rate in treatment-naïve CLL, with 95.5% 36-month progression-free survival (PFS) in R/R CLL and deep, durable responses in R/R MCL. These results underscore BeOne’s vision of enabling fixed-duration therapy leading to treatment-free remission across B-cell cancers.
4min read
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Business Development
BoAn Biotechnology Licenses US Rights for Dulaglutide Injection BA5101
BoAn Biotechnology announced on June 11 a licensing agreement granting its partner the rights to commercialize dulaglutide injection BA5101 in the United States, including regulatory filings and sales. BoAn will receive upfront payments, milestone payments, and sales royalties. BA5101, approved in China in August 2025, is the world’s first and only approved biosimilar to Trulicity® and has received FDA clearance to initiate clinical trials in the U.S. With Trulicity® generating $2.914 billion in U.S. sales in 2025 and the U.S. diabetes patient population projected to reach 43 million by 2050, this strategic partnership aims to enhance access to this once-weekly GLP-1 receptor agonist and capture significant market share in the growing diabetes therapeutics space.
2min read
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Innovation
Bispecific Dual-Payload ADC: A Dual Upgrade in Antibody-Drug Conjugates — Three Companies Enter Clinical Stage
Bispecific dual-payload antibody-drug conjugates (ADCs) represent a cutting-edge advancement in oncology, combining bispecific targeting and dual cytotoxic payloads to overcome tumor heterogeneity and drug resistance. Three Chinese pharmaceutical companies—Hangzhou DAC Biotech, Innovent Biologics, and Alphamab Oncology—have now entered the clinical stage with their respective bispecific dual-payload ADC candidates, marking a significant milestone in China’s innovative drug development. Their pipelines feature unique target combinations, distinct payload mechanisms, and advanced conjugation technologies, positioning this dual-upgraded ADC approach as a promising next frontier in solid tumor therapy.
2min read
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Innovation
BeOne Medicines Reports Multiple Clinical Data; Halts 6 Pipeline Programs
BeOne Medicines (BeiGene, 688235.SH) announced the discontinuation of six in-development pipeline programs while presenting promising clinical data from three key oncology assets at the 2026 ASCO Annual Meeting. The strategic move aims to concentrate resources on high-potential candidates, including a CDK4 inhibitor now in global Phase III for first-line HR+/HER2- breast cancer, a B7-H4 antibody-drug conjugate advancing to Phase III in ovarian cancer, and a GPC3/4-1BB bispecific antibody showing near-standard-of-care efficacy in advanced hepatocellular carcinoma. Analysts view the portfolio consolidation positively, with CICC issuing an 'Outperform' rating and a ¥320 CNY target price.
3min read
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Research-led
Multiple Dimensions
Updated Quarterly
High-quality Chinese Assets Selected