You can share it to WeChat via the Qr code.
Enter the applet sharing event using WeChat scan.
Driven by rapid advancements in science and technology and increasing global health demands, CGT is emerging as a transformative force in biopharma. Moving from the lab to clinical applications, it is providing innovative solutions for diseases that traditional therapies struggle to address, including hereditary disorders, cancer, and rare diseases. The market is expected to reach $30.539 billion by 2025, with projections surpassing $100 billion by 2030.
Although the Chinese market is relatively new to the CGT field, it benefits from unique IIT research capabilities that are accelerating the transition of cutting-edge CGT technologies from the lab to clinical practice. The first domestically developed stem cell and gene therapies are expected to be approved and enter the market by 2025. However, CGT products are costly, with limited medical insurance coverage and relatively low patient affordability and willingness to pay. Facing challenges such as limited market size, high costs, long-term safety concerns, complex production processes, and payment difficulties, the industry must address several critical questions: How can the range of indication audience for CGT expand beyond rare diseases? How can we develop the most cost-effective CGT products through innovation and technological advancement? How can we accelerate the translation of druggable cutting-edge therapies and clinical applications? How can cooperation be accelerated to find IO Combo strategies that achieve greater-than-additive effects in treating solid tumors? How can we break into overseas markets to embrace global growth? These challenges are becoming inevitable focal points for the CGT industry as it seeks to overcome barriers and drive forward transformative advancements.
IGC is one of the earliest in-depth conventions in China dedicated to the innovation and translation of cutting-edge therapies. Over the past eight years, as the fields of immunotherapy, cell therapy, and gene therapy have grown in China, IGC 2025 will return to Beijing. This edition will kick off with six specialized forums aimed at addressing technological challenges and emerging topics of CGT, mRNA vaccines and drugs, immunotherapy antibodies and combination therapies while facilitating discussions on cutting-edge therapies, including advanced technologies, innovative therapy development, leading translations, clinical progress, and strategies for international registration. The goal is to foster deeper communication and cooperation across industry, academia, research, and medicine both domestically and internationally, accelerating the industrial translation of immunotherapies, gene therapies, and cell therapies in China.
曲光博士现任诺洁贝生物联合创始人、首席运营官。
曲光博士于美国俄亥俄州立大学获得博士学位,并在基因治疗著名专家James Wilson教授实验室开展博士后相关工作,拥有30多年的基因治疗药物的开发经验。曾先后在美国最早的基因治疗公司Avigen 和CHOP(费城儿童医院)病毒载体中心任职、负责病毒载体大规模制备的工艺与新技术开发。
2013年,Spark Therapeutic成立,曲光博士作为该公司负责病毒载体制备工艺与新技术开发的Head负责其所有产品的工艺开发,主导了全球第一个眼科用基因治疗产品Luxturna(2018年FDA批准)从实验室到获批上市销售的全过程的生产工艺开发与建立,同时制备了全球最早开展的由宾西法尼亚大学的Car June博士主导的CAR-T疗法中使用的慢病毒载体。
截至目前,曲光博士主导工艺开发的基因治疗产品中1个已经获批上市,2个目前正处于临床III期试验、3个处于临床I期试验。
鲁凤民,北京大学基础医学院病原生物学系主任、北京大学人民医院肝病研究所教授。研究方向为乙肝病毒及相关肝病的新指标和新技术研究。作为负责人先后承担科技部重大专项、重点研发、国自然面上项目以及北京市科委重大项目等,两次获得国家科技进步二等奖,作为第一完成人获得中华医学科技二等奖1次。以通讯作者在国内外期刊发表研究论文近二百篇,获批发明专利19项。
Refund Description: