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IGC is the earliest in-depth forum in China focusing on the innovation and transformation of cutting-edge therapeutic technologies. With the growth of China's cutting-edge therapy industry such as cell therapy and gene therapy, IGC has witnessed the development of China's novel cell therapy, gene therapy and immunotherapy industries after 7 years, and has become the most influential CGT industry brand annual meeting in China.
With the continuous research and development and clinical breakthroughs in the field of cell and gene therapy, cell and gene therapy is one of the hottest investment areas in the current medical field. Because of its unique IIT research properties, CGT accelerates various cutting-edge CGT technologies from the laboratory to the clinic. However, the rapid transformation and development of the CGT industry is also faced with high costs, long-term security, complex production, payment difficulties and other challenges.
IGC 2024 (8th Immunotherapy, Gene Therapy and Cell Therapy Convention) will be upgraded again at the Beijing International Convention Center! This year, the IGC will start from the 14 subdivision forums, discuss the Investment strategy, Forward-looking technology, Innovative therapy research and development, Leading transformation, Advanced process quality control, and Domestic and Foreign application strategy of immune cell therapy, Gene therapy, Stem cell therapy, Exosome therapy, Tumor Vaccine, and Organoid technology to promote in-depth exchanges and cooperation between domestic and foreign industry, university, research and medical research, and to further accelerate the industrial transformation of immunotherapy, gene therapy and cell therapy across the region.
From industrial strategy, academic exchange to industrialization practice, grasp the lifeblood from forward-looking innovative technology to CGT drug transformation, industrialization and commercialization:
★ Insight into the future of CGT technology: gene editing, synthetic biology, iPSC, LNP-mRNA, exosomes, AAV, etc., to accelerate cutting-edge therapeutic transformation
★ Creating CGT products with cost advantages: in vivo cell therapy, universal cell therapy, CAR-NK, TILs, iPSC stem cell therapy, gene editing therapy, AAV gene therapy drugs, tumor vaccines and other product R&D innovation, process innovation, and production equipment innovation
★ Accelerating CGT transformation and clinical research and development: from solid tumors of blood tumors to more extended exploration of autoimmune, neurological and chronic diseases
★ Getting through the last mile to market: MSC stem cell drugs, AAV gene therapy, in vitro gene editing therapy, CAR T/NK BLA declaration analysis
Prof Xianmin Zeng received her PhD in Molecular Biology from the Technical University of Denmark in 2000 and had her postdoctoral training at the National Institutes of Health (NIH), USA in 2000-2005. She joined the faculty of the Buck Institute for Research on Aging in 2005 where she was Professor from 2005-2018.
Prof Zeng is a renowned stem cell biologist and neurobiologist with expertise in the development of pluripotent stem cell (PSC)-based therapy and drug discovery. One of her research focuses is to study neural development in human and to model neurodegenerative diseases using patient-specific and genome edited isogenic PSC lines. A biotech entrepreneur with >100 peer-reviewed publications, Prof Zeng is a well-established and internationally recognized leader in the creation of disease models for drug discovery. Prof. Zeng is a recipient of a major translational grant to develop clinically grade dopaminergic neurons from pluripotent stem cells (PSC) for Parkinson’s disease from California Institute for Regenerative Medicine (https://www.cirm.ca.gov/our-progress/people/xianmin-zeng), and iPSC-based toxicity screen grant from the NIH.
Prof Zeng is the Founder and CEO of RxCell Inc, a US-based biotechnology company focused on therapeutic applications of PSC, and Visiting Professor at the National University of Singapore School of Medicine.
上海长征医院副院长、器官移植暨肝脏外科主任、全军器官移植研究所所长、博导; n国家重点学科/国家临床重点专科/全军临床重点专科 学科带头人;
上海市领军人才、芝加哥大学访问学者;历任上海市人大代表、黄浦区卫健委副主任等;
亚洲胰腺暨胰岛移植协会(APITA)主席、国家卫健委妇幼司儿童及青少年糖尿病防治专委会副主任、中华医学会器官移植分会胰腺小肠胰岛移植学组副组长/异种移植学组委员、中国康复医学会器官移植专委会青工委副主任、上海市胰岛移植临床质控暨培训基地主任、市医学会器官移植专科分会常委兼秘书、市生物工程学会细胞治疗专委会副主委等;
师从彭承宏、傅志仁教授,长期从事器官移植及肝胆胰腺外科,建立了我国最主要的胰岛移植中心,开展例数/疗效均居国内第一;开展世界首例自体再生胰岛移植、亚洲首例机器人全胰腺切除+自体胰岛移植、上海市首例DCD胰岛联合肾移植/首例儿童胰岛移植等;
主笔胰岛移植领域“国家卫健委管理规范及质控标准、上海质控标准”等;
主持20余项课题及人才计划,获上海市创新创业大赛一等奖、银蛇奖、曙光学者等。
原北京大学药学院院长、天然药物与仿生药物全国重点实验室主任、北大宁波药物研究院院长;国家973项目、基金委创新群体、国家创新药物重大专项首席科学家。长期从事基于化学-生物学交叉的新药发现新技术新方法研究,在Science、Nature Biotech等杂志发表论文百余篇,其中活流感病毒疫苗研究入选国际疫苗学会“Paper of the Year”、中国科学十大进展等。
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。
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