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細胞與基因治療研發及生產工藝論壇2020二輪通知
點擊次數:2311 發布日期:2019-12-26  來源:本站 本站原創,轉載請注明出處
細胞與基因治療研發及生產工藝論壇2020
 
為推動來源于中國及亞太地區的研發創新、開放式創新及研發外部合作模式、藥物研發外部合作及加速新藥研發策略、探索免疫腫瘤藥品開發與戰略合作新模式,由上海迪易商務咨詢有限公司/Deliver Life Sciences 主辦、大費城美中醫藥協會SAPA-GP 支持籌辦的2020亞太藥物研發領袖峰會 (‘APRDL 2020’)將如期在上海舉行,為國內外專家高端交流、產業與資本對接搭建平臺。
 
會議網站:www.aprdl2020.com
會議時間:2020年4月15-16日
會議地點:上海錦江湯臣洲際酒店
 
會議規模:
● 80+ 國內外知名演講嘉賓 & 500+ 專業高層參會代表
● 70%+核心市?。ㄖ饕?來源于中國及全球的生物醫藥公司、醫院、學術機構)參會者
● 60%+公司決策層及總監級別以上參會者
● 2天高層峰會+定制化且提前預留安排的一對一交流會議+8小時的合作交流及茶歇午宴+1場雞尾酒晚宴
 
部分已確認的峰會演講嘉賓
 
隨著美國和歐洲監管部門最近批準細胞和基因療法的上市,以及一系列細胞和基因療法正在向監管審查邁進,人們越來越關注這些復雜的生物療法的商業生產環節。一直以來,生產制造都是細胞和基因治療公司面臨的最大挑戰之一。此次亞太藥物研發領袖峰會 (APRDL 2020) 組委會特別針對細胞與基因治療生產制造工藝邀請到來自全球頂級研究機構、跨國制藥公司以及創新生物技術企業共同參與并分享。
 
Confirmed Speakers & Hot Topics
 
The CAR-T PIONEER PLENARY KEYNOTE SPEECH
 
 
Stephan Grupp教授
腫瘤科細胞治療和移植科主任, 干細胞實驗室的醫學主任, 主治醫師和腫瘤學研究員, 兒科教授, 費城兒童醫院 (CHOP), 賓夕法尼亞大學佩雷爾曼醫學院, 科學顧問委員會成員, 西比曼生物科技集團
Stephan Grupp, MD PhD, is the Chief of the Cellular Therapy and Transplant Section, Director of the Cancer Immunotherapy Program, and Medical Director of The Cell and Gene Therapy Lab at the Children’s Hospital of Philadelphia (CHOP), as well as the Yetta Dietch Novotny Professor of Pediatrics at the University of Pennsylvania Perelman School of Medicine.
Dr. Grupp graduated from the University of Cincinnati after completing the MD/PhD program with a PhD in Immunology.
He completed pediatric residency at the Boston Children’s Hospital, followed by a fellowship in Pediatric Hematology/Oncology at the Dana Farber Cancer Institute and postdoctoral work in Immunology at Harvard University. He then joined the faculty at Harvard University until 1996, when he came to CHOP. His primary area of clinical research is the use of CAR T and other engineered cell therapies in relapsed pediatric cancers. He led all of the pediatric ALL trials of CTL019 (now approved as Kymriah), including the largest and most successful engineered T cell therapy clinical trial conducted to date (1, 2), as well as the global registration trial for CTL019 (3). As a result of this work, he presented the Clinical Perspective at the July 2018 FDA ODAC meeting, at which reviewers voted 10-0 for recommendation of approval for Kymriah in pediatric ALL. His primary laboratory interest is the development of new cell therapy treatments for pediatric cancers. Dr. Grupp is a reviewer for several journals and the author of over 200 peer-reviewed journal articles, as well as numerous abstracts and book chapters.
主題演講:The CAR-T Cell Revolution -- CAR T-Cell Therapy targeting Leukemia, Lymphoma, and Future Hopes for Solid Tumors
 
Travis Young 教授
生物制品部副總裁, 美國California Institute for Biomedical Research ( Calibr ), 美國The Scripps Research Institute ( TSRI )
Dr. Travis Young is the Vice President of Biologics at Calibr, a division of Scripps Research, where he was a member of Calibr’s founding principal investigators.  He currently serves as the lead investigator on multiple bench-to-bedside antibody and cellular therapy-based programs.   Dr. Young maintains a research group focused in the development of novel therapeutics at the interface between protein engineering and synthetic biology.  This research spans multiple disease indications including cancer, autoimmune, metabolic disorders, and infectious disease.  His work has been highly awarded and received support from the Wellcome Trust, NIH (National Cancer Institute), Department of Defense, Mesothelioma Research foundation, American Cancer Society, among others, in addition to receiving backing from major pharma groups which supports clinical translation of programs.  His work has resulted in numerous publications and patents with ~2000 citations in the past 5 years.  He received a BS in biochemistry from Boston College and a PhD in chemical biology from The Scripps Research Institute as an ARCS scholar.  At Scripps, his work was foundational for the development of programs in the Calibr pipeline today, including a bispecific antibody for prostate cancer which will enter clinical trials next year.  After receiving his PhD, he completed a postdoc at Harvard Medical School with an NIH fellowship, in the department of Biological Chemistry and Molecular Pharmacology.
主題演講:Controllable CAR-T Cell Therapy
 
CELL THERAPY BIOPROCESSING & CMC, REGULATORY & QUALITY CONTROL
 
Xiu-Yan Wang 博士
聯席主任, 邁克爾哈里斯細胞療法和細胞工程實驗室, 分子藥理學部門主要研究員
美國紀念斯隆-凱特琳癌癥中心
Dr. Wang was trained by Dr. Adolfo García-Sastre and received her Ph.D. in Biomedical Sciences from the Mount Sinai School of Medicine in NYC. She joined Dr. Peter Cresswell’s laboratory in the Department of Immunology at Yale University as a Howard Hughes Medical Institute fellow, and later as a Cancer Research Institute postdoctoral associate. Dr. Wang joined Memorial Sloan Kettering Cancer Center in 2007, and is currently an Associate Lab Member in Department of Molecular Pharmacology, and the Assistant Director of the Michael G Harris Cell Therapy and Cell Engineering Facility. Dr. Wang is in charge of the R&D, process development and manufacturing. She has overseen the successful manufacturing of all the CAR T cell products used in 13 phase I/II clinical trials as well as over 20 batches of cGMP grade viral vectors. She served in the translational science and product development committee in the American Society of Gene and Cell Therapy (ASGCT). She is currently a member for the National Heart, Lung and Blood Institute (NHLBI) independent external panel and a committee member for the Alliance of Regenerate Medicine (ARM) and the National Institute for Innovation in Manufacturing Biopharmaceuticals (NIIMBL).
主題演講:The State of the ART of Manufacturing CAR T Cells and The Latest Advancements
Abstract: The approval of CAR-T cell therapy for ALL and NHL by FDA has led to increased academic and industrial interest for this therapy. The success of this promising therapy relies on reproducible manufacturing of high-quality clinical-grade CAR T cells. We have established a robust modular CAR-T manufacturing platform as well as a clinical grade retroviral vector manufacturing process, which allowed us to manufacture hundreds of CAR-T cell products and support 12 phase I/II CAR-T cell clinical trials successfully at our center. Over the years, we have made improvement of our existing manufacturing platform and tested new manufacturing procedures that supported the products meeting all critical quality attributes. We have generated T cells expressing CARs encoded by gammaretroviral vectors starting from either healthy donors or cryopreserved patient apheresis products using Prodigy. Moreover, the emergence of CRISPR-Cas and iPSC technologies has pointed new directions for CAR-T cell manufacturing.
--  Define the central role of CAR-T cell manufacturing for the clinical applications of CAR-T cell therapies
--  Summarize the current CAR-T cell manufacturing platforms (modular and continuous)
--  MSK experience for CAR-T manufacturing and evolvement of our manufacturing platform
--  Manufacturing of large-scale clinical grade retroviral vectors for CAR-T cell therapy
--  Quality control for clinical grade retroviral vector and CAR-T cell manufacturing
 
Steve Oh 教授
研究院教授, 主任, 干細胞治療工程研究中心
生物工程技術研究院, 新加坡科技研究局 ( A*STAR )
Dr. Steve Oh obtained his PhD from Birmingham University, UK (1990) and is the Director of Stem Cell Bioprocessing and Institute Scientist, Stem Cell Group. He holds several industry leadership roles e.g. Past Vice President of International Society of Cell and Gene Therapy (ISCT); Member of International Society of Stem Cell Research (ISSCR); Member of International Stem Cell Banking Initiative (ISCBI); Vice President of Stem Cell Society Singapore (SCSS). He is also an Adjunct Associate Professor at NTU, PhD Supervisor at A*STAR Graduate Academy and has received research funding grants ranging from SGD 10 to 25 million. He has 42 Patents, granted and pending, 107 scientific publications, written the book “Sensational Stem Cell: How to cure medical complications.” and created 2 companies: Veristem and Zenzic Labs.
Our research is focused on human adult and pluripotent stem cell bioprocessing. Our team has developed a range of patent families for the manufacture of mesenchymal stem cells, reprogrammed human induced pluripotent stem cells and created neural cells, cardiomyocytes, blood cells, cartilage, bone and retinal pigment epithelial cells at bioreactor scale using a range of microcarrier technologies including biodegradable ones. Most recently, we have achieved a novel method of directed differentiation using CRISPR technology that will accelerate therapeutic applications of stem cells. A complimentary technology that has been developed is the use of microfluidics for separations of cell and particulates.
主題演講:A Broad Technology Platform for Reprogramming, Expansion of Pluripotent Stem Cells and Differentiation to Cell & Gene Therapies
Abstract: The BTI, at A*STAR has developed a Broad Technology Platform for Reprogramming, Expansion of Pluripotent Stem Cells and Differentiation to Cell Therapies. The IPS-SpheresTM technology is capable of automating the reprogramming of 4 different cell sources: T cells, haematopoietic stem cells, fibroblasts and mesenchymal stem cells into human induced pluripotent stem cells. From each reprogramming campaign, we can select up to 96 wells of clones to characterize and pick the best growing clone that can be cultured in suspension cultures and differentiated to target lineages.
Using the microcarrier technology IPS-SpheresTM, BTi has been able to demonstrate production of neuroprogenitors and neurons at 10 million cells/ml. These neurons have been demonstrated to be functional in mouse and rat animal models of Parkinson’s disease with rapid recovery times within 3 to 6 months depending on the cell dose. Secondly, BTI has cardiomyocytes in a completely defined serum free media with 2 small molecules achieving 8 million cells/ml in a suspension bioreactor. Cardiomyocytes have been implanted in pig models of cardiac infarction. Most recently, BTi has manufactured CD34+ haematopoietic progenitors from hiPSC on this platform achieving 2 million cells/ml, these have been further differentiated to universal O negative Rhesus negative RBCs (17 million cells/ml.) and are being tested in animal models of acute anaemia. This platform is broadly available for scale up of pluripotent stem cell therapies to meet the global shortage of cells for therapies.
 
Yoji Sato 教授
細胞治療產品部主任兼首席科學家, 日本國立健康科學研究中心 NIHS 
[ Head, Division of Cell-Based Therapeutic Products, National Institute of Health Sciences, Japan ]
Dr. Yoji Sato is Head of Division of Cell-Based Therapeutic Products, National Institute of Health Sciences. Dr. Sato is also an Adjunct Professor of Nagoya City University, a Guest Professor of Osaka University, and an Adjunct Professor of Kyushu University. He received his Ph.D. in Pharmaceutical Science from the University of Tokyo. While a post-doctoral fellow at the University of Cincinnati College of Medicine, he succeeded in establishing a variety of transgenic animal models to elucidate mechanisms of cardiac excitation-contraction coupling and heart failure. Dr. Sato’s current research area is in the field of regulatory science for the quality and safety of advanced cell-based therapeutic products (CTPs). He is currently leading a public-private partnership initiative in Japan for validation of test methods for tumorigenicity assessment of CTPs. He is also serving as Vice Chair of Database Committee, the Japanese Society for Regenerative Medicine, which provides the National Regenerative Medicine Database (NRMD), a nation-wide patient registry system for CTPs, and as a member of Technical Committees, Panel on Science and Technology, Health Science Council, the Japan Ministry of Health Labour and Welfare.
主題演講:Regulations and Platforms for Ensuring the Quality, Safety and Efficacy of Cell Therapy Products in Japan
 
Sergio Fracchia 博士
全球 RegCMC 總監, Kymriah 全球生產和質量控制負責人, 細胞和基因療法
瑞士諾華 [ Global regCMC Director ]
Sergio presently works as Associate Director RegCMC – Cell and Gene Therapy at Novartis.  He is presently RegCMC representative for the development of several gene therapy and gene editing investigational medicinal products at different stage of development.
From 2001 to 2016 he covered the position of Regulatory Affairs Manager in Molmed (Milan), where he lead RegCMC manufacturing, non-clinical and clinical development of more than 15 cell and gene therapy investigational medicinal products through their entire life cycle.
In the position Sergio followed the development and registration of the three major cell and gene therapy products currently approved as well as the world-wide licensing program of Kymriah.
He started his professional life with 1 year post-doctoral research in biochemistry, followed by 15 years of experience at Merck/Serono where he worked in a laboratory focussed on cell bank analytics and characterization.
Formal education includes a MSc in Biology and a PhD in Biotechnology.
主題演講:The Kymriah Story: Challenges, Headaches and Solutions on Manufacturing and Quality Control
 
Wen Bo Wang 博士
高級副總裁, 技術運營, Fate Therapeutics 
[ Senior VicePresident, Technical Operations ]
Dr. Wen Bo Wang is Senior Vice President, Technical Operations at Fate Therapeutics, overseeing the company’s manufacturing strategies for its pipeline of off-the-shelf cell-based cancer immunotherapy candidates and scaling the Company’s induced pluripotent stem cell iPSC platform to support late-stage clinical and commercial operations. She was formerly Senior Vice President Cell Therapy R&D at Fujifilm Cellular Dynamics Inc (FCDI), where she was responsible for developing the cell therapy R&D strategy and the iPSC based pipeline products and led the next generation production technology development efforts. Previously, she was VP Process Sciences, and directed scale up and scale out platform process development for iPSC based iCell products and MyCell products including automation and bioreactor work. Prior to joining FCDI in 2008, Dr. Wang was Group Leader, Process Sciences, at Geron Corporation, Menlo Park, CA working with embryonic stem cell derived cell therapies and dendritic cell cancer vaccine. From 2001 to 2005, Dr Wang held a number of positions at ViaCell, Boston, MA including Associate Scientific Director, ViaCord Human Umbilical Cord Blood Bank (a subdivision of ViaCell). Dr. Wang serves on the board of directors for Standards Coordinating Body and as US expert at the US Technical Advisory Group (US TAG) for ISO TC/276 Biotechnology. Dr. Wang earned a B.S. in Biology from Ocean University of Qingdao, P.R. China and received her Ph.D. in Biology from Newcastle University, United Kingdom. She conducted post-doctoral training in Cryobiology at Biosciences Research Laboratory, USDA/Agricultural Research Service, Fargo, N.D.
主題演講:Developing Allogeneic Cancer Immunotherapy with iPSC Technology
--  Fate is pioneering a revolutionary approach to cell therapy -- we use renewable master induced pluripotent stem cell (iPSC) lines generated from our proprietary iPSC platform to derive cell therapy product candidates that can be delivered off-the-shelf for the treatment of a large number of patients.
--  Our cell therapy product candidate pipeline is comprised of immuno-oncology programs, including off-the-shelf NK- and T-cell product candidates derived from master iPSC lines.
--  Discuss challenges in cell culture scale up for allogeneic cell therapies with iPSC technology
 
Yajin ( Jenny ) Ni 博士
高級總監, 工藝和產品開發, 技術運營, Allogene Therapeutics 
[ Process & Product Development, Technical Operations]
Dr. Ni is Senior Director, Process & Product Development at Allogene Therapeutics, leading the company’s manufacturing process development activities for its pipeline of off-the-shelf CART candidates. During her tenure at Allogeneic Therapeutics and previously at Pfizer from 2015 to now, she has led her team to establish platform allogeneic CART manufacturing processes for enabling pipeline programs quickly advancing to early clinical testing using robust enough 1st generation process and transiting to late stage clinical & commercial manufacturing using more controlled 2nd generation automated & closed process. From 2000 to 2010 she held a senior technical role at VIRxSYS, where she conducted pioneering adaptive T cell therapy development work using lentiviral vector modified autologous CD4 T cells for HIV infection together with Dr. Carl June’s lab at the University of Pennsylvania. Through that work,  they were 1st to bring lentiviral vector modified autologous adoptive T cell therapy into the clinic, and 1st to demonstrate feasibility of large scale GMP manufacturing of lentiviral vector and ex vivo expansion of gene-modified T cells in WAVE bioreactor. That work also accumulated a large set of patient safety data for lentiviral vector modified adaptive T cell therapy and laid down the groundwork for lentivector modified autologous CART therapy to be first tested in the clinic by Dr. Carl June’s lab. Dr. Ni earned a M.D. in internal medicine from the Kunming Medical College, P.R. China and received her Ph.D. in virology from the Kyoto University, Japan. She then conducted post-doctoral training in gene delivery at the NIH, USA before embarking on her gene & cell therapy product development career in both small biotech and big pharma.
主題演講:Cell Therapy Bioprocessing and Allogeneic Manufacturing Solutions for Cell Therapy Products
 
Harry Lam 博士
執行副總裁, 技術運營主管, 上海藥明巨諾生物科技有限公司 
[ Executive Vice President of Technical Operations ]
Dr. Harry Lam is currently Executive Vice President, Head of Technical Operations at JW Therapeutics. Previously, he was VP, Head of Biologics Manufacturing at Sanofi; VP, Manufacturing and Technical Operations, Progenitor Cell Therapy (PCT), A Subsidiary of Hitachi Chemical Advanced Therapeutics Solutions; and VP, Manufacturing and Process Development, at Shire Regenerative Medicine.
Prior to Shire, Dr. Lam spent 17 years at Genentech, where he held a variety of positions with increasing responsibilities, including Director of Manufacturing & Technology, Genentech Singapore Pte Ltd; Senior Director, Global Head of Biologics Drug Substance Manufacturing Science & Technology; and Roche Global Head of Contract Manufacturing Operations, Commercial Drug Substance. Prior to joining Genentech, Dr. Lam spent 11 years at Pfizer in the Bioprocess R&D department.
Harry received his B.S. in Chemical Engineering from the University of Birmingham, UK and his Ph.D. in Chemical Engineering from Rensselaer Polytechnic Institute, NY.
主題演講:Cell Therapy Manufacturing Commercialization -- Strategy and Challenges
--  Unique Manufacturing Challenges for Autologous Cell Therapy
--  IND to Commercial: A Paradigm Shift
--  Development By Design
--  Quality By Design
--  Cell Therapy COGs Optimization
--  IND to Commercial: Scale-out Challenge
--  Cell Therapy Technology Road Map Vision
--  Current Weakness in the Technology Landscape
--  Final Thoughts
 
王立群 博士
首席執行官, 復星凱特生物科技有限公司
 [ Chief Executive Officer, Fosun Kite Biotechnology ]
Richard received degrees of B.S of Cell Biology from the University of Science & Technology of China, Ph.D. of Molecular Biology from the University of Maryland, Baltimore and MBA from Xavier University, Cincinnati in the US. He obtained his post-doctoral training at the National Institutes of Health, Baltimore, USA.
Richard now is the CEO of Fosun Kite Biotechnology. Taking a combined approach of internal R&D and external partnering/technology transfer, Fosun Kite is dedicated to the advancement of innovative cell therapy and its industrialization in China to benefit patients.
Richard is very experienced in biopharmaceutical industry. Having spent close to 20 years in R&D and management positions in both the US and China, he has taken senior roles and increasing leadership responsibilities in Procter & Gamble Pharmaceutical, Bristol-Myers Squibb in the US, AstraZeneca Innovation Center and GSK R&D Center in China. Prior to Fosun Kite, Richard was the Chief Operation Officer of Cellular Biomedicine Group (NASDAQ: CBMG), where he was in charge of the company’s immunotherapy pipeline including manufacturing, clinical development and registration, and the stem cell business unit.
主題演講:Revolution of CAR-T Cell Therapies – Regulatory and Commercialization Considerations for Yescarta in China
 
張宇 博士
聯合創始人 兼 首席執行官, 頤昂生物
[ Co-Founder and Chief Executive Officer, Aeon Therapeutics ]
Dr. Zhang Yu is the president and CEO of Aeon Therapeutics Inc., a joint-venture biotech company established by Eureka Therapeutics Inc. and Vcanbio Cell&Gene Engineering Co.,Ltd. Prior to found Aeon, Dr. Zhang acted as assistant president and senior strategic planning expert in Vcanbio. Dr. Zhang received his B.S. in Bioengineering and M.S. in Biomedical Engineering from Beihang University, and Ph.D. in Stem Cell and Regenerative Medicine from Heinrich-Heine-Universität Düsseldorf in Germany. Before the industrial career, he worked in Rhine Forum, University of Applied Sciences Bonn-Rhein-Sieg, and was a visiting scholar in German Aerospace Center and University of Palermo. He is a member of German Society of Stem Cell, Chinese Society of Cell Biology, and reviewer of several journals, e.g. Current Stem Cell Research&Therapy. Dr. Zhang was the winner of “131 talent plan”and “Tianjin Green Card Plan”.
主題演講:The Aeon experience of translating and developing a FIC&FIH CAR-T product in China
-- The Regulatory of Cell & Gene product in China: Poc or IND
-- Key CMC strategy: manual & automatic system in PoC and IND
-- the Aeon experience in fast translating FIC&FIH product in China
 
劉必佐 先生
首席執行官 兼 首席財務官, 西比曼生物科技集團
[ Chief Executive Officer & Chief Financial Officer, Cellular Biomedicine Group ]
Mr. Liu formerly served as the Corporate Vice President at Alibaba Group responsible for Alibaba’s overseas investments. Since joining Alibaba in 2009, Tony held various positions including Corporate Vice President at B2B corporate investment, corporate finance, and General Manager for the B2C global e-commerce platform. He was also Chief Financial Officer for HiChina, a subsidiary of Alibaba, a leading internet infrastructure service provider.
Prior to joining Alibaba, Tony spent 19 years at Microsoft Corporation where he served in a variety of finance leadership roles. He was the General Manager of Corporate Strategy looking after Microsoft’s China investment strategy and corporate strategic planning process. Tony was a key leader in the Microsoft corporate finance department during the 1990s as the Corporate Accounting Director. He was well recognized within Microsoft for driving an efficient worldwide finance consolidation, reporting, internal management accounting policy process, and showcased Microsoft’s best practices to many Fortune 500 companies in the U.S.
Mr. Liu obtained his Washington State CPA certificate in 1992. He had been serving as an Independent Director and Chairman of the Audit Committee for CBMG since March 2013 and was appointed as Chief Financial Officer in January 2014. He was appointed as Chief Executive Officer of the Company in February 2016.
主題演講:CBMG Commercialization Strategies for Cell and Gene Therapies; Particularly in China
-- What China can bring to advancing the manufacture process in novel therapy modalities
-- Manufacturing capabilities: addressing the “ Achilles heel “ of cell therapy
-- The importance of strategic collaborations to improve manufacturing
 
楊林 博士
首席執行官, 博生吉醫藥科技(蘇州)有限公司
 [ Chief Executive Officer, PersonGen BioTherapeutics (Suzhou) ]
Dr. Lin Yang is currently a Distinguished Professor at the Cyrus Tang Hematology Center of Soochow University, China, and an adjunct professor of Department of Lymphoma and Myeloma at the MD Anderson Cancer Center, USA. Dr. Yang is the founder/chairman/chief scientific officer of PersonGen BioTherapeutics (Suzhou) Co., Ltd., and Chairman/CEO of PersonGen-Anke Cellular Therapeutics Co., Ltd. Dr. Yang received many awards, including Innovation and Entrepreneurship Talent of Jiangsu Province, Six Peak Talent of Jiangsu Province, Gusu Innovation and Entrepreneur Leading Talent, Pioneer of Suzhou Industrial Park Technology, Nanjing “321” Technology Leaders, Second Prize of China Innovation and Entrepreneurship Competition, and many other honorary titles and awards. He has published more than 70 research articles in recognized peer reviewed journals, such as Cancer Cell, Cancer Research, Oncogene, JBC, and Cancer Science, etc., which were all funded by international, national and provincial foundations.
As a principle investigator, Dr. Yang plays a major role in the immunotherapy of CAR-T cells and CAR-NK cells of China, and has obtained impressive achievements in the industrialization and clinical trials of CAR-T cell therapy. Among them, several clinical trials are the first-in human projects performed globally, including CAR-T cell therapy for T-cell acute lymphoblastic leukemia, and 4th generation CAR-T cell therapy for solid tumors. Led by Dr. Yang, PersonGen-Anke’s CD19-CAR-T product has been submitted to Chinese FDA and is being under the evaluation process which is expected an approval from CFDA within next few months.
主題演講:Automated Manufacturing of Chimeric Antigen Receptor T Cells
Abstract: The chimeric antigen receptor gene-modified T cells (CAR-T cells) technology has been proven clinically successful since 2010, especially targeting CD19 molecules in the treatment of refractory, relapsed B cell-derived malignancies in which the clinical efficacy has never been achieved by traditional tumor therapy strategies, and become the most attractive area in cancer immunotherapy. However, CAR-T cell technology has been experiencing huge challenges, including the expensive preparation and quality control costs for CAR-T cells and lacking clinically verified automated and closed technology. In another word, current mainstream technology hugely relies on highly skillful personnel that increases risk of contamination and production failure, and brings uncertainty for its industrialization. In this presentation, Dr. Yang will analyze the development trend based on his team’s effort in this area, and summarize how applying automated platform to CAR-T cell manufacturing will prompt CAR-T cell technology industrialization and lead to clinical success.
 
 
Yajin ( Jenny ) Ni 博士
高級總監, 工藝和產品開發, 技術運營, Allogene Therapeutics 
俞磊 博士
首席執行官, 上海優卡迪生物醫藥科技張宇 博士
聯合創始人兼首席執行官, 頤昂生物 
Stephen Lim 博士
首席執行官, 來恩生物醫藥
何霆 博士
首席執行官, 北京藝妙神州醫藥科技有限公司
Li Zhou 博士
細胞療法和抗體研究 副總裁, 綠葉制藥波士頓研發中心
小組討論: Establishing a Robust, Scalable, Automated, Functionally-closed Manufacturing Process to Support a Pipeline of Emerging CAR-T Cell Immunotherapy
-- Overcome the viral vector supply bottleneck for the clinical development timeline
-- Overcome the equipment capacity limitation for implementing a robust automated & closed processing
-- How to manufacturing a large batch of allogeneic CAR T drug product with homogeneity and a robust post thaw recovery
-- Overcome the starting cell source limitation & variation, how to secure an unlimited, identical, clean cells (free of human viruse infection) for allogeneic CAR T product manufacturing;
 
 
Stephan Grupp教授
腫瘤科細胞治療和移植科主任, 干細胞實驗室的醫學主任, 主治醫師和腫瘤學研究員, 兒科教授, 費城兒童醫院 (CHOP), 賓夕法尼亞大學佩雷爾曼醫學院; 科學顧問委員會成員, 西比曼生物科技集團
趙陽賓 教授
細胞免疫療法中心, T細胞工程實驗室 主任, 美國賓夕法尼亞大學醫學院
Yoji Sato教授
細胞治療產品部主任兼首席科學家, 日本國立健康科學研究中心 NIHS 
Travis Young 教授
生物制品部副總裁, 美國California Institute for Biomedical Research ( Calibr ), 美國The Scripps Research Institute ( TSRI )
Sergio Fracchia 博士
全球 RegCMC 總監, Kymriah 全球生產和質量控制負責人, 細胞和基因療法, 瑞士諾華
John Rossi 博士
轉換科學總監, 凱特制藥, 吉利德科學子公司
劉誠 博士
創始人兼首席執行官, 優瑞科生物技術公司
圓桌討論: Global CAR-T Pioneers Fireside Chat: Revolution and Strengthening Academia-Industry Collaboration for Development Next Generation CAR T-Cell Therapies
 
Corporate Sponsors
 
 
Hermann Bohnenkamp 博士
VP Business Development APAC
Miltenyi Biotec
As Vice President of Business Development APAC at Miltenyi Biotec, Hermann is responsible for Miltenyi’s strategic collaborations with Biotech and Pharma in Cell and Gene Therapy (CGT) in Asia. Joining Miltenyi Biotec in 2009, he was instrumental in building Miltenyi’s cell and gene therapy business as Business Area Manager, including the release of key ancillary materials and the T Cell Transduction Prodigy platform. In 2016 he led Miltenyi’s Australian business as Managing Director. Before joining Miltenyi, Hermann was responsible for the project management for early drug and monoclonal antibody development at MediGene Immunotherapies, Munich. He holds a doctoral degree from the University of Bonn and the Helmholtz Research Center Juelich for studies on bioprocess development of DCs and ACT in solid tumor indications. He continued similar studies at King’s College London (Guy’s Hospital) with Cancer Research UK.
Silvio Weber 博士
Head of the Industrial Process Development Team
Miltenyi Biotec
As the Head of the Industrial Process Development Team at Miltenyi Biotec, Silvio is responsible to provide automated Cell and Gene Therapy procedures on the CliniMACS Prodigy for industrial customers. Silvio has more than 10 years of R&D experience in various fields of cell biology, including Immunology, Regenerative Medicine and Pharmacology. After joining Miltenyi, Silvio has been coordinating custom-tailored development of automated processes for T-cell mediated Immunotherapy, Stem Cell Engineering and other innovative Cell and Gene Therapy approaches using the Miltenyi Biotec CliniMACS Prodigy platform. Silvio holds a Diploma degree in Biochemistry from the University of Bielefeld and a Doctoral degree in Biochemistry from the University of Kiel.
主題演講:Towards commercialization – accomplish the challenges of cell and gene therapies
--  Review how manufacturing processes can affect quality attributes of living drug products
--  Considerations of a fully automated cell manufacturing process in the context of process transfer
--  Assess industry collaboration strategies
 
Pete Gagnon 博士
CSO, BIA Separations
Pete Gagnon is a widely respected global authority in the field of downstream processing. He is the author or more than 100 scientific publications and inventor on more than 100 awarded patents in the United States, Europe, and Asia. His expertise covers purification of monoclonal antibodies, virus particles, extra-cellular vesicles, plasmid DNA, and mRNA. He is currently Chief Scientific Officer at BIA Separations, a European manufacturer of specialized chromatography media for purification of gene therapy products.
主題演講:A Cornerstone Industrial Purification Platform for Exosomes
Abstract: Exosome-based therapies are already in advanced clinical trials as many new applications beckon. This highlights a need for a simple effective purification platform that maximizes probability for clinical success and hastens the path to market. This presentation will share detailed case studies with extensive analytical support, illustrating a broadly applicable platform approach for purifying exosomes from all cell culture sources. Removal of host cell DNA, host proteins, virus, and endotoxins will be discussed.
Exosomes are quickly evolving as next-generation candidates for regenerative therapy but manufacturing technology lags behind.
--  The antibody industry demonstrated the value of a platform approach to purification. A similar approach is needed for exosomes.
--  This presentation will describe a scalable platform that can be used as a cornerstone to purify exosomes from all cell cultures.
--  It particularly focuses on removal of chromatin since chromatin interferes with both purification efficiency and product quality.
--  New high throughput analytical methods combining multi-angle light scattering and immunofluorescence will also be presented.
 
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