
Fosun Kite, Axicabtagene Ciloleucel Injection
June 2021
Fosun Kite’s anti-CD19 autologous CAR-T cell therapy product, Yikaida® (axicabtagene ciloleucel injection), has been approved for marketing, becoming the first cell therapy product approved for commercialization in China.
JW Therapeutics, Relmacabtagene Autoleucel Injection
September 2021
JW Therapeutics’ Relma-cel Injection Approved for Marketing, Becoming the Second CAR-T Therapy Approved in China After Fosun Kite’s Axi-cel Injection and the First Domestically Produced CAR-T Product Approved in the Country
Heyuan Bio, Nacinalcabtagene Autoleucel Injection
November 2023
Healios’ Naxicabtagene Autoleucel Injection Approved for Market Launch, Becoming China’s First CAR-T Product for the Treatment of Adult Relapsed or Refractory B-cell Acute Lymphoblastic Leukemia
CARsgen Therapeutics, Zevorcabtagene Autoleucel Injection
March 2024
Carsgen Therapeutics’ Zevor-cel Injection Approved for Marketing, Becoming China’s First CAR-T Product for the Treatment of Relapsed or Refractory Multiple Myeloma
Caribou Biosciences, Ikiocel Injection
June 2023
Reindeer Biologics’ Icilucabtagene Autoleucel Injection has received NMPA approval for marketing, indicated for the treatment of adult patients with relapsed or refractory multiple myeloma who have progressed after at least three prior lines of therapy; it is the world’s first approved fully human BCMA CAR-T cell therapy product.
Legend Biotech, Cilta-cel Injection
August 2024
Legend Biotech’s cilta-cel injection has been approved, marking the first domestically produced CAR-T therapy in China for the treatment of adult patients with relapsed or refractory multiple myeloma;
Platinum Biotech, Emicizumab Injection
January 2025
Platinum Life Sciences’ emicizumab injection approved for market launch, indicated for acute graft-versus-host disease (aGVHD) with predominant gastrointestinal involvement in patients aged 14 years and older who have failed corticosteroid therapy, becoming China’s first approved stem cell therapy
BeiGene, AAV Gene Therapy
April 2025
Xinjiu Nian® (bopenadacogene etaparvovec injection), an AAV gene therapy from Belief Medical, has received marketing approval, becoming the first approved gene therapy for hemophilia B in China and the first approved gene therapy for rare diseases nationwide.
In recent years, China’s cell and gene therapy (CGT) industry has advanced with remarkable momentum, celebrating the approvals of numerous “first-in-China” products and witnessing historic breakthroughs with “first-in-the-world” therapies. Behind these milestone achievements lie sustained technological innovation by enterprises, robust capital support, and precise regulatory oversight.
However, behind this booming development lie numerous pressing challenges that urgently need to be addressed:
1.
Extremely high technical barriers, such as the off-target effects of gene-editing technologies and the risk of random integration or proto-oncogene activation by viral vectors, leading to abnormal cell proliferation
2.
Due to the inherent characteristics of long R&D cycles and high costs, many enterprises face the dilemma of being unable to advance projects due to funding shortages.
3.
Complexities in Clinical Trial Design: Patient Physiological Characteristics, Ethical Issues, Long-Term Efficacy Assessment, and Safety Monitoring
4.
Inadequate interpretation of policies leads to missed policy dividends
........
These factors collectively constitute constraints on corporate development. How to strike a dynamic balance between technological optimization and commercialization is a critical challenge that every cell and gene therapy (CGT) company must confront.
ThroughChokepoints in core technologies, cash flow shortages, complexities in clinical development, and regulatory bottlenecks within the ecosystemThereafter, we have sufficient confidence and conviction that domestic CGT companies can develop more first-in-China and even first-in-global products.
In this context, to help the CGT industry break through scientific research bottlenecks, promote enterprise development, facilitate integration across the industrial chain, and accelerate the translation of scientific and technological achievements, VCBeat, in collaboration with CSGCT, willMay 10, 2025InSuzhou International Expo CenterAt the 2025 VBEF Future Healthcare & Pharma Top 100 Exhibition, a special “Forum on Innovation and Emerging Opportunities in the CGT Industry & Launch Press Conference of the 2025 CSGCT Annual Meeting”. The forum will inviteInternational and Domestic Industry Experts, CGT Innovative Enterprises, Clinical Experts, Investment Institutions, and Industrial Investorsetc., will focus onLatest Industry Trends, Policy Interpretations, Innovative Technologies, Key Challenges and Bottlenecks, and New Opportunities in Investment and Business DevelopmentIn-depth discussions on such topics to promote the high-quality development of the CGT industry。
Forum Information
Time: All day on May 10, 2025
Location: Suzhou International Expo Center (during the VBEF Conference)
Scale: 100 people
Organizational Structure
Organizers: VCBeat, CSGCT
Supporting Organizations: Youlin Pharmaceutical, Boya Life,Yeasen Biotechnology
Attendees
Innovative pharmaceutical companies and CDMOs in the CGT sector,BiotechEnterprises, industry associations, and industrial parks; USD and RMB funds focused on the CGT sector; and strategic investors.
Speaker
Dr. Han Haixiong
Personal Profile:
Wei Qing
Boyacell Stem Cell Technology Co., Ltd.
Senior ResearcherPersonal Profile:
Director of Exosome Technology R&D and Senior Researcher at Boya Stem Cell Technology Co., Ltd. Participated in multiple national and Tianjin municipal projects, with extensive experience in new drug applications and IND approvals for mesenchymal stem cells. Possesses clinical application and regulatory submission experience for automated cell therapy equipment, and currently leads Boya’sExosome TechnologyProcess R&D, with extensive experience in FDA Drug Master File (DMF) submissions for exosome drug substances and International Nomenclature of Cosmetic Ingredients (INCI) registrations. Engaged in long-term innovative research and development of processes for stem cells, immune cells, and exosomes. Holds over 10 granted patents as the primary inventor and has published multiple papers as the first or sole author in core provincial and ministerial-level journals in China. Recipient of the Excellence Award at the 2nd China Postdoctoral Innovation and Entrepreneurship Competition and the Gold Award at the 4th Tianjin Postdoctoral Innovation and Entrepreneurship Competition.Liu Chen
Managing Director
Personal Profile:
Currently the Head of China and Managing Director at Locust Walk. Locust Walk is a globally leading investment bank in the biopharmaceutical sector, specializing in licensing, mergers and acquisitions, and capital raising within the biopharmaceutical industry. With deep insights into the deal landscape of the biopharmaceutical sector, he has provided valuable support for the strategic development of international companies in China. Liu Chen holds a research background in colorectal cancer stem cells from the University of Oxford and earned an MBA in Finance jointly from Tsinghua University and Cornell University. He previously worked in clinical development and regulatory affairs at international pharmaceutical companies, with professional experience spanning Europe, the United States, and Asia. He currently serves as a mentor at the Cornell Center for Life Sciences Venture Capital and will be a Visiting Scholar at Harvard University in 2025.Reindeer Bio
Chief Innovation and Investment Officer
Personal Profile:
Responsible for incubating and investing in Reindeer Bio’s innovative business ventures, with a focus on upstream and downstream incubation across the cell and gene therapy (CGT) industry chain. Previously, Dr. Xie, as a co-founder, incubated and invested in a genetic engineering vector vaccine platform, establishing multi-pipeline companies targeting two major markets—vaccines for livestock and pets, and human vaccines—to meet the demands for import substitution and industrial upgrading. As a co-founder, he also built a synthetic biology platform targeting agriculture, medical aesthetics,Functional FoodsHe has established multi-pipeline companies in these fields, exploring innovative growth drivers for biotechnology beyond pharmaceuticals. Additionally, as a co-founder, he has incubated cutting-edge technology platforms such as mRNA, siRNA, and phage therapy. Previously, Dr. Xie served as the Founding Partner of TVM Capital’s China office, focusing on cross-border equity investments and technology transfer in the field of innovative drugs.Zhu Fangfang
BloodJi Biology
Founder
Personal Profile:
Zhu Fangfang, Ph.D. from Peking University and Postdoctoral Fellow at Stanford University, is a Tenure-Track Associate Professor at Shanghai Jiao Tong University and the Founder of Suzhou Xueji Biotechnology Co., Ltd. She has been recognized as a National-Level Talent and a High-Level Innovative and Entrepreneurial Talent in Jiangsu Province. Additionally, she has received numerous honors, including the 2025 New Era Youth Pioneer Award from the Central Committee of the Communist Youth League of China and the All-China Youth Federation, Chief Scientist at the National Center for Technological Innovation of Biopharmaceuticals, and a spot on the Forbes China·100 Elite Returnees list. With 17 years of research experience in the field of stem cells, she holds multiple invention patents in China, the United States, and internationally. In 2021, she returned to China to establish Xueji Biotechnology, which has emerged as a potential unicorn enterprise in China.Zhao Piming
Daoji Genomics
Founder
Personal Profile:
Zhang Liang
Personal Profile:
Niu Jing
Personal Profile:
Meeting Agenda

Conference Registration
Interested enterprises and industry peers are welcome to scan the QR code below to register, or add the event assistant on WeChat for inquiries about event details and content.


