Institute Professor and Director, Stem Cell Group
Bioprocessing Technology Institute, 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.
Professor and Chairman of the Department of Basic Medical Sciences
School of Medicine
Dr. Xin Lin currently is a Professor and the Chairman of the Department of Basic Medical Sciences in Tsinghua University Medical School. Dr. Xin Lin obtained his Ph.D. degree from University of Texas Health Science Center in Houston in 1995. Following a postdoctoral training in UCSF/Gladstone Institutes in San Francisco, Dr. Lin started as an Assistant Professor in the State University of New York at Buffalo in 2000. In 2004 he was recruited to the University of Texas MD Anderson Cancer Center as an Associate Professor. Subsequently, he was promoted to Professor and then Endowed Professor in the University of Texas MD Anderson Cancer Center before his returning to China. He has been studying the molecular mechanism of signal transduction controlling lymphocyte activation, and their impacts on inflammation and anti-microbial and anti-cancer responses. Currently, his lab is developing therapeutic approaches using TCR-T/CAR-T cell methods to target cancer and viral infection.
Dr. Luk is the CEO at Neurophth Therapeutics, Inc. Prior to joining Neurophth, he has served as Senior Vice President and Chief Medical Officer at Shanghai Henlius Biotech, Inc., and he has also held executive roles at various MNCs such as Spark Therapeutics, Inc., Biogen Idec-Hemophilia (acquired by Sanofi), Bayer Schering Pharma LLC., Avigen, Inc.(acquired by Genzyme Corporation) and Tularik, Inc. (acquired by Amgen, Inc.) since 1998. Until 2003, his early researches were primarily investigating gene regulation and expression with the emphasis on rare diseases, oncological diseases, biologics and regenerative medicines. He served on the Clinical Design Committee for rare disease at the U.S. Food and Drug Administration focusing on adaptive clinical trial design to shorten drug development timeline between 2006 and 2009. Under his leadership in strategic drug development, he has won regulatory marketing approvals of 16 products in neurology, ophthalmology, gene/cell therapy, hematology and cancer therapy as of today.
Dr. Luk has published more than 85 book chapters, scientific and medical articles in highly regarded peer-reviewed journals, including New England Journal of Medicine, Nature, Cell, and Science, and is an inventor on over 10 patent applications. Dr. Luk holds an MBA from the Harvard Business School. He is ACRP-certified in clinical research and also received his Ph.D. in Neuroscience from the University of California San Francisco Medical School as well as bachelor’s degree in Molecular and Cell Biology from the University of California Berkeley in the United States.
Chief Technical Operation Officer
Dr. Su Xiao currently serves as the Chief Technical Operation Officer of Neurophth and she has served as a co-founder and board member of Neurophth since 2019. She has ten years of experience in translational sciences, early and late stage gene therapy development and manufacturing of biologics. Her goal is to make gene therapy affordable and accessible and she has primarily worked for organizations both large and small, including gene therapy development at Pfizer and National Institutes of Health and GMP manufacturing at Vigene Biosciences. She received her B.S. in Chemical Engineering from Tsinghua University and Ph.D. in Chemical and Biomolecular Engineering from the Johns Hopkins University.
Chief Executive Officer
Dr. Ting He is the founder and CEO of Immunochina Pharmaceuticals. Dr. He received his B.S. in biology from Xiamen University and Ph.D. in cancer biology from Tsinghua University. With years of experience in basic research of cancer immunology, he is dedicated to develop innovative CAR-T therapy for treatment of cancer. He was awarded Beijing Nova program and Beijing Eagle Talents.
CEO of Biologics Development Business Unit
Dr. Min graduated from the University of California at Berkeley majoring in Molecular Biology in 1991 and held a Ph.D. in Molecular Biology from the University of California at Los Angeles in 1997. Dr. Min’s expertise includes biologics development from discovery to manufacturing as well as strategic planning and business development.
Dr. Min worked at Amgen in the U.S. as a principal scientist for over 10 years. He was in charge of biologics discovery and optimization, developing multiple protein therapeutics that are currently in clinical trials or on the market. After that, Dr. Min joined Samsung Advanced Institute of Technology. In that job, he worked as the Head of Antibody Engineering responsible for the development of a novel antibody-based therapeutic platform and as a leader for the oncology therapeutic development program. From 2010 to 2011, he carried out the responsibilities as Oncology Program Director in Biosimilar Group and Vice President of Strategic Business Development Group, focusing on antibody biosimilars development. From 2012 to 2017, he worked as Vice President of Process Team at Samsung Bioepis Co., Ltd. With responsibilities covering a full range of upstream and downstream process development, as well as tech transfer and GMP production. Just before joining GenScript, in 2018, Dr. Min worked at the Drug Substance Team of Samsung Bioepis Co, Ltd. as a senior Vice President, leading the process development of all biosimilars and new biologics in Samsung’s pipeline.
President and Chief Scientific Officer
Guangdong Xiangxue Life Sciences
Yi Li, Ph.D. University of Leicester, UK, the National Distinguished Expert, Leading Talent of Guangdong Province, President and CSO of Guangdong Xiangxue Life Sciences, LTD, Principal Investigator of Center for Infection & Immunity at Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, PI at the State Key Laboratory of Respiratory Diseases. He has been engaged in the development of antibody and T cell receptor drugs in the UK for a long time. Representative papers have been published in Nature Biotechnology, Nature Medicine, JBC, Molecular Cancer Therapy, etc. He pioneered the application of phage display technology to the directed evolution of T cell receptors. He developed the world first human high-affinity soluble TCR, which the affinity for recognizing pHLA was increased by more than one million times as a key breakthrough in the field of TCR. Under his leadership his team has successfully developed a number of high-affinity TCRs at Immunocore in the UK, which has eventually been used in FDA-approved immunotherapy clinical research products. In 2012, he returned to China and led the establishment of China's first high-affinity TCR-mediated T cell therapy platform. The TCR-T product TAEST16001 injection developed by the Xiangxue team has obtained the first TCR-T IND approved by CDE of the National Medical Products Administration.
Founder and Chief Executive Officer
Nanjing CART Medical Technology
CAR-T therapy specialist, technical core personel in Carl June group at UPENN. Dr. Wang has long engaged in CAR design-evaluation, he is the participant in the first CAR-T drug R&D. He takes the lead in solid tumor CAR design and achieved recognition. He accomplished two solid tumor CAR-T patents together with Dr. Carl June and Dr. Michael Milone.
After returning to China, he finished the early exploration of donor CAR-T infusion for ALL patient and got succuess. Now Dr. Wang's team has been authorized two patents for invention. 25 patents application has been accepted by SIPO(State Intellectual Property Office). Multiple IIT clinical trials with Dr. Wang's CAR-T products have been carried out both in hematologic malignancies and solid tumors treatment.
VP Business Development APAC
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.
Head of the Industrial Process Development Team
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.
Vice President, General Manager, Cell Drug Business Unit
Shanghai Cell Therapy Group
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.
Chief Medical Officer IASO Biotherapeutics
Dr. Wen (Maxwell) Wang currently is the Chief Medical Officer in IASO Biotherapeutics Co., Ltd. He obtained his M.D. degree in Wuerzburg University in Germany and Ph.D. degree from University of Aberdeen in UK and then did his postdoctoral training in at UConn Health Center in USA.
Dr. Wang has over 7 years of experience in Chinese Leading cell therapy companies including JW Therapeutics, Cellular Biomedicine Group (Nasdaq: CBMG) in clinical, preclinical, and translational development including CART cell and stem cell therapy. He held one of leading position in the 1st Chinese CD19-targeted CART cell and Mesenchymal Stem Cell INDs.
Before industry career, Dr. Wang worked as a Resident and Attending in Orthopedic Department in Shanghai TCM Hospital for 5 years.
Shenzhen Institute for Innovation and Translational Medicine
Dr. Mingjun Wang，Executive President of Shenzhen Institute for Innovation and Translational Medicine, received his MD from Anhui Medical University in China and his PhD degree in Cellular Immunology from the University of Copenhagen in Denmark in 2009, and finished his postdoctoral training in cancer immunology at Baylor College of Medicine in Houston of the United States. His research is focused on identification of cancer antigens and the development of T cell-based cancer immunotherapy using TIL, TCR-T cells or CAR-T cells for various types of malignancies. Dr. Mingjun Wang has published more than 30 peer-reviewed papers and three book chapters in the field of cancer immunology.
Chief Executive Officer
Nanjing KAEDI Biotech
Paul received his PhD from Shanghai Institutes for Biological Sciences, CAS, in 2007 and then initiated his postdoctoral researches from 2008 to 2013 in US. After that, he joined the Genscript as senior scientist and then director of Department.
Paul now is the CEO and founder of Nanjing KAEDI Biotechnology. Charging a combined strategy of internal synthetic biology technology platform new drug R&D and external partnering/technology transfer, KAEDI is dedicated to the advancement of innovative cell therapy and its industrialization in China to benefit solid tumor patients.
As a leader of Nanjing KAEDI Biotech Inc. Dr. Dai and Colleagues developed multiple next generation innovative CAR molecules for solid tumors therapy. Breakthrough progresses of CAR-T preclinical research published in Journal for ImmunoTherapy of Cancer and Cancer Immunology Research, total impact factor >18. POC clinical and IND registration are progressing smoothly.
Executive Vice President, Head of Technical Operations JW Therapeutics
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.
Chief Executive Officer Lion TCR Pte Ltd
Stephen Lim is currently the Chief Executive Officer of Lion TCR Pte Ltd, a biotech company with assets in TCR-T & Gene Editing technologies. Stephen has more than 20 years of experience managing business in China including setting up nationwide distribution network for new medical device in China. He currently sits on the board of BioCheetah Pte Ltd, a medical diagnostic company in bladder and prostate cancer diagnostics.
Wong Tee Wee
Director of Operations Lion TCR Pte Ltd
Dr. Tee Wee WONG is the Director of Operations at LionTCR, Singapore.
He received his Ph.D. in Pharmacology from the University of Sydney, Australia.
He has over 20 years of pharmaceutical industry experiences in the area of Manufacturing, Regulatory Affairs, Clinical Development, Quality Assurance and Quality Control with demonstrated history of working in pharmaceutical start-ups. His experiences included working as a Regulatory Consultant with the Health Sciences Authority, Singapore.
His start up experiences included a biotechnology company manufacturing novel drug delivery systems for the eye, and the manufacturing of plasma derived products. He was responsible for garnering the GMP Certification for these companies, and garnering product registration of their products. At LionTCR, he is responsible for commissioning and qualifying the newly constructed GMP facility, ensure the facility comply with cGMP guidelines, and the manufacturing of clinical research material for use in clinical trials.
Dr. Xu was graduated from the Department of Medicine, Southern Medical University (formerly First Military Medical University) in 1985 and obtained a master's degree from Beijing Medical University, a Ph.D. degree in Medical School of the University of Bern in Switzerland, and a postdoctoral fellow at Columbia University and the University of Pennsylvania.
Dr. Xu is the former Senior Scientist, Project Manager for CAR-T projects at the University of Pennsylvania; and currently a Distinguished Professor of Translational Hepatology Institute at Capital Medical University in Beijing, and the Executive Director of the Sino-US Joint Translational Hepatology Research Center at this institute.
Dr. Xu now serves as the member of expert group for "cell and gene therapy products regulatory policy" for cFDA. Also, Dr. Xu is the Founder, Chairman and Chief Scientist of Bioceltech Therapeutics Co., Ltd.
In 1991, as a pioneer, Dr. Xu initiated the study on the Retrovirus-introduced Suicide Gene Therapy on Gastric Cancer using HSV-TK / GCV System at the 3rd Hospital of Beijing Medical University, which was reported first in an international gastric cancer congress.
In 1993-1994, Dr. Xu carried out clinical trial of multi-functional immune stem cells on advanced cancer patients, which made Dr. Xu one of the easiest domestic scientists in cancer immune cell therapy;
In 1996, Dr. Xu was invited to conduct the research of CAR-T cell therapy on gastric cancer in Japan, which led Dr. Xu one of the earliest CAR-T research scientists in the world.
In 2005, with rich experience in CAR-T and gene therapy, Dr. Xu was invited as a Senior Scientist and Research Project Manager by Professor Carl June at the Abramson Cancer Center at the University of Pennsylvania. Dr. Xu was responsible for the construction of the applicable CAR-T structure and cell system, and the improvement, quality control and management of a highly efficient lentiviral vector production process.
As one of the earliest project managers for UPenn's CAR-T cell therapy program, Dr. Xu designed and constructed a number of CAR-T vectors, among which the second generation of CAR-T-CD19 and CAR-T-Mesothelin have been screened out and approved by the FDA for clinical trials for advanced tumors. Exciting clinical results have been achieved, including the cured Emily Whitehead, a leukemia child in the United States.
The achievement was elected as one of the top 10 technological breakthroughs in the world by Science magazine in 2013, and patient Emily was interviewed by US President Barack Obama.
The CAR-T-CD19 declared by Novartis was received FDA approval (product name: Kymriah) on August 30, 2017, becoming the world's first CAR-T live cell drug.
The high-titer and high transfection rate of lentivirus production application system established by Dr. Xu has been used by many famous laboratories in the United States, making a special contribution to the successful clinical application of this project.
In August 2016, the allogeneic CAR-T therapy approach with HLA haploidentical donor T cell, jointly developed from the cooperation between Dr. Xu's team and the team led by Dr. Xiaojun Huang, Director of Research Institute of Hematology, Peking University People's Hospital, successfully cured a 3-year-old Chinese child with recurrent and refractory leukemia. This success story has opened up a new area for allogeneic CAR-T applications. Currently, the patient has been done with one-time treatment for over 16 months, without tumor recurrence investigated at both of morphology and molecular biology level, making the project a leading position globally. This allo-CAR-T therapy was called “Beijing Approach” by colleagues in the field.
CEO 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.
Chief Executive Officer
UniCAR-Therapy Bio-Medicine Technology
Yu Lei, M.D. / Ph.D., is currently a “Zijiang” Distinguish Professor, Director of the Institute of the Biomedical Engineering and Technology (iBET), East China Normal University, China. He is also a member of Shanghai Pharmaceutical Committee, and member of China Clinical-Research Society of Cell Therapy Specialized Committee; At same time, Dr. Yu was also appointed an Adjunct Professor, Department of Chemical Pharmaceutical and Pharmaceutical and Department of Biological Engineering, University of Utah, US. Dr. Yu is an interdisciplinary experiences in medicine, clinical practice, basic medical research, translational medicine, pharmaceutical research, as well as a successful entrepreneur.
Wei (William) Cao
Founder, Chairman and CEO Gracell Biotechnologies
Dr. Wei (William) Cao is the founder, chairman and CEO of Gracell Biotechnologies Co., Ltd. Together with an industry veteran team, Dr. Cao has created Gracell to capture special opportunity of cell therapy for global market. Through external partnership and in-house R&D effort, Gracell has been rapidly progressing with novel CAR-T programs to address the industry’s key issues and also the research and development of stem cell therapies.
Dr. Cao has over 30 years of professional experience in scientific research, products development and startups. He was the co-founder and CEO of a Nasdaq listed cellular therapy company. Prior to his venture, Dr Cao served as Technical Manager for Bayer Diagnostics Asia Pacific region, and China General Manager of Affymetrix, a world leader in genetic analysis industry.
Dr. Cao earned a Bachelor’s degree in Medicine from Fudan University Medical College, China and a PhD degree in Pharmacology from Medical College of Virginia, USA. He has extensive research experience in immune-pharmacology field at Harvard Medical School and Stanford University Medical Center. He is invited as the director of International Chinese Stem Cell Foundation (ICSCF), and served as Venture Partner of 6 Dimensions Capital. Dr. Cao received prestigious White Magnolia Award from Shanghai City.
Dr. Cao is also an inventor of more than 70 patents in the field of stem cell and CAR-T technologies.
Dr. Lyu Lulu obtained her Ph.D. in clinical medicine (internal medicine, hematology) in 2006. Prior to 2007, she mainly undertook the clinical and scientific research on hematopoietic and mesenchymal stem cells. In 2001, Dr. Lyu participated in the first umbilical cord blood transplantation in China for the treatment of childhood leukemia. She pioneered and established the domestic technology of isolating mesenchymal stem cells from the umbilical cord in 2004. In the following year, she continued her research on hematopoietic cell transplantation and mesenchymal stem cells at Westchester Medical Center of New York Medical College. Dr. Lyu published various papers in domestic and international journals. After joining a multinational pharmaceutical company in 2007, Dr. Lyu was engaged in the research and development of innovative drugs and the strategic planning for new products in the fields of hematology and oncology for more than a decade. With key appointments being held in multinational companies including Novartis, Genzyme, Roche, AstraZeneca, and Merck, she has garnered a wealth of experience in R&D and product life-cycle management in the areas of targeted drugs, immunotherapy, and cell therapy. In addition, she has played a vital role in the R&D, registration, and market expansion of ground-breaking products for treating cancers such as Gleevec®, Herceptin®, Tagrisso®, and Keytruda®. In June 2018, Dr. Lyu left the international pharmaceutical corporate world to become a trailblazer focusing on the development of innovative drugs domestically. As the current CEO of Juventas Cell Therapy Ltd., she is committed to promoting the clinical research of cell therapy and to pushing forward the industrialization thereof, thus creating world-leading products based on cell therapy.
Founder and CEO
Dr. Cheng Liu is the founder and CEO of Eureka Therapeutics. Prior to founding Eureka, Dr. Liu was a Principal Scientist in antibody drug discovery at Chiron (now Novartis), where he championed anti-CSF1 antibody program for treatment of bone metastasis to human clinical trials. He is the inventor of multiple issued US patents in drug discovery. In 2007, he was awarded Special US Congressional Recognition for his contributions to improving human health. Dr. Liu received his B.S. in Cell Biology and Genetics from Beijing University and a PhD in Molecular Cell Biology from the University of California, Berkeley.
Co-Founder and Chief Executive Officer
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”.
Tony (Bizuo) Liu
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.
President and Chief Executive Officer
Henry Ji, Ph.D., co-founded and has served as a director of Sorrento since January 2006, and as its Chief Executive Officer and President since September 2012. Dr. Ji served as Sorrento’s Chief Scientific Officer from November 2008 to September 2012 and as its Interim Chief Executive Officer from April 2011 to September 2012.
Dr. Ji served as VP of Sales and Business Development at CombiMatrix, and was responsible for strategic technology alliances. From 1999 to 2001, Dr. Ji served as Director of Business Development, and in 2001 as VP of Business Development at Stratagene (later acquired by Agilent Technologies), a biotechnology company. In 1997, Dr. Ji co-founded Stratagene Genomics, a wholly-owned subsidiary of Stratagene Corporation, and served as its President and Chief Executive Officer and Director from its founding until 1999.
Dr. Ji obtained his Ph.D. in Animal Physiology from the University of Minnesota and a B.S. in Biochemistry from Fudan University. He held many executive positions in biotechnology and life sciences companies during his career.
Founder & Chief Scientific Officer
Hebei Senlang Biotech
Jianqiang Li is currently the Founder and Chief Science Officer of Hebei Senlang Biotech, a company focuses on the development and clinical translation of next generation cell therapy technology. Dr. Li obtained his PhD degree from University of Wuerzburg in Germany. He did his postdoctoral training at City of Hope and Fred Hutchinson CRC. His expertise covered the following fields: Gene modified adoptive T cell therapy; In vitro expansion and gene editing of Hematopoietic stem cells; Transplant Immunology.
Founder and Chairman
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.
Chief Scientific Officer
The Pregene Biopharma Company
As the Chief Scientific Officer in Shenzhen PREGENE Biopharma Company, Ltd, Dr. Zhang Jishuai graduated from Zhengzhou University, receiving a B.S. degree in clinical medicine. Then, he got his M.S. degree in molecular immunology in the Fourth Military Medical University, and Ph.D. in genetics in Beijing Institute of Biotechnology. After that, he obtained the postdoctoral training in the Hormel Institute in the University of Minnesota.
As an expert on tumor biology, Dr. Zhang once did detailed study on tumor gene function (including tumor initiation, differentiation and metastasis), about which he published over 20 papers. In 2016, he founded the PREGENE Company and acted as the Chief Scientific Officer, from which he began the research and development of CART drug. Having built a platform of “Nanobody discovery, CART research and drug development”, PREGENE is now mainly focused on CART therapy for hematologic tumors.
Chief Strategy Officer
SCG Cell Therapy Pte Ltd
Christy Ma is the Chief Strategy Officer at SCG Cell Therapy Pte Ltd, a Singapore based biotechnology company focusing on the development of immunotherapy to prevent and cure viral-related diseases.
Christy specialties in oncology and immunotherapy drug development. Before joining SCG, she served in various positions in Clinical Operations and Pharmacovigilance, with participation in the development of Talzenna® (talazoparib), Cabiralizumab in combination with Opdivo® (nivolumab), Herceptin® (trastuzumab) and Avastin® (bevacizumab). She successfully managed Phase I – III global clinical trials.
Christy received her B.S. degree in Chemical Biology from University of California, Berkeley and holds her M.S. in Medical Product Development Management from San Jose State University.
Deputy Director, Clinical Diagnostic Dept.
Director, Flow Cytometry Lab
Lu Daopei Medical Group
Hui Wang, MD, is the Deputy Director of the Clinical Diagnostic Department(vice chairman grade), and Director of Flow Cytometry Lab at the Ludaopei Medical Group, as well as Director, CEO, and CMO of Synarc Research Laboratory (Beijing) Ltd.
Dr. Wang graduated from the Peking University Health Science Center.
She completed internal medical residency at the Beijing Shijitan Hospital, followed by a fellowship in Hematology Institute at the People’s hospital. She then joined the faculty at Ludaopei Medical Group in 2008. She primary area of clinical research is the clinical diagnosis of flow cytometry. Having been worked in flow cytometry field for 18 years, She has signed more than 300,000 diagnostic reports of immunophenotyping and MRD detection, of which more than 40% coming from other hospitals around China.
She has taken part in writing 10 professional books, given nearly 600 professional oral presentations in 29 provinces of China(including Taiwan). She has hundreds of students from over 100 well-known hospitals, distributed in 26 provinces of China (including Taiwan).
The chairman of flow cytometry branch of professional committee on laboratory medicine, Chinese association of integrated traditional and western medicine
The vice chairman of blood & body fluid branch of Beijing Medical Laboratory Society
The standing committee member of hematology branch of Chinese non-public Medical Association
The standing committee member of Chinese flow cytometry Union
The member and special expert of lymphoma branch of Chinese Anti-cancer Association, flow cytometry branch of Chinese society of hematology and immunology, cell analysis special committee of Chinese society of bioengineering, and other societies.
President and Chief Executive Officer
Asclepius Technology Company Group ( ATCG Corp )
Huashun Li MD & PhD is the founder of ATCG Corp.based in Suzhou,Dr. Huashun Li graduated from the Second Military Medical University in Shanghai, China in 1986. He got his master degree from the PLA General Hospital in Beijing in 1989. He was a visiting scholar in Johns Hopkins University School of Medicine, Baltimore, Maryland, USA from 1991 to 1994. He did the PhD dissertation in the laboratory of Dr. Yi Rao in the Department of Anatomy & Neurobiology from 1994 to 1999, and received his PhD from Washington University School of Medicine in St. Louis, Missouri, USA in 1999. He was a postdoctoral fellow in the laboratories of Drs. Yuh Nung Jan and Lily Jan in the Department of Physiology, Howard Hughes Medical Institute at the University of California San Francisco from 1999 to 2005.
He has been an assistant professor in Developmental Neurobiology Program in the Institute of Molecular Medicine and Genetics at the Medical College of Georgia, Augusta, Georgia, USA since 2005. He was recruited to become a founding director of West China Developmental & Stem Cell Institute at Sichuan University in 2007, and has become the founding director of SARITE Center for Stem Cell Engineering Translational Medicine in Shanghai East Hospital Tongji University School of Medicine.
Dr. Jijun Yuan is co-founder and chief executive officer of Shanghai Genbase Biotechnology Co. Ltd, which was established in 2015 to focus on developing new therapeutic drugs, including cell therapies, gene therapies and therapeutic antibodies. Prior to that, Dr. Jijun Yuan spent six years at Shanghai Hengrui Pharmaceutical Co. as the associate director in charge of the biological division. He has been involved in more than 30 drug discovery programs, including oncology, diabetes and cardiovascular therapeutic drugs.
Dr. Jijun Yuan holds a PhD degree in molecular biology from Ohio State University and worked as postdoctoral researcher at University of California Los Angeles.
Chief of the Cellular Therapy and Transplant Section, Director of the Cancer Immunotherapy Program, Medical Director of The Cell and Gene Therapy Lab Children’s Hospital of Philadelphia (CHOP)
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.
Director, T Cell Engineering Laboratory, Center for Cellular Immunotherapies
University of Pennsylvania School of Medicine
Dr. Yangbing Zhao is an Associate Professor and the Director of the T Cell Engineering Laboratory (TCEL), Center for Cellular Immunotherapies at the University of Pennsylvania. He received an MD and PhD in Immunology from the Third Medical University in Chongqing, China. From 1996 – 2000, he was a visiting scientist at The Weizmann Institute of Science in Rehovot, Israel, where he studied tolerance induction through genetically engineered T cells allogeneic bone marrow transplantation. For the next two years he was a research associate at Duke University Medical Center, where he worked on RNA transfected dendritic cell vaccines against cancers. In 2003, he joined Dr. Steven Rosenberg’s group as a senior research fellow at the Surgery Branch of the National Cancer Institute, where his research work directly led to clinical trials of treating cancer patients with T cells against Mart1, NY-ESO-1, Her2/Neu, CD19 (Yescarta) and VEGFR. He joined the faculty of the Department of Pathology and Laboratory Medicine, University of Pennsylvania in 2009 as the Director of TCEL. his research work at the University of Pennsylvania led to clinical trials to treat cancer patients with TCRT or CART against NY-ESO-1, CD19 (kymriah), Mesothelin, cMet, GD2 and CD123, as well as first in human CRISPR/CAS9 application in the world. Dr. Zhao has more than 20 years’ experiences in T cell engineering with over 50 publications and filed over 90 patents in the CART field. Dr. Zhao is the scientific co-founder of Tmunity Therapeutics.
Assistant Director, Michael G.Harris Cell Therapy and Cell Engineering Facility
Associate Laboratory Member, Department of Molecular Pharmacology Memorial Sloan Kettering Cancer Center
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).
Yajin (Jenny) Ni
Senior Director, Process & Product Development, Technical Operations Allogene Therapeutics
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.
Wen Bo Wang
Senior Vice President, Technical Operations Fate Therapeutics
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.
Kerry L. Blanchard
Chief Executive Officer Everest Medicines
Dr. Blanchard’s career spans four decades in diverse leadership roles across North America and Asia. In February 2020 he was appointed as CEO of Everest Medicines after having served as Operating Partner at CBC Group, a healthcare private equity firm and one of the leading investors in Everest Medicines, since November 2019. Prior to CBC Group, he was Chief Science Officer at Innovent Biologics, where he oversaw the NDA preparation and submission for the company’s PD1 antibody, sintilimab, which was approved in late 2018 and launched in China in 2019 and led the partnership efforts with Incyte to develop three small molecule oncology assets for Greater China. Previously, Dr. Blanchard was the Senior Vice President of Lilly China Drug Development and External Innovation, where he built and led the development and medical affairs teams, who designed and implemented clinical plans for assets across all therapeutic areas. He also built and executed the company’s external partnership drug development portfolio model in China. He positioned Lilly to capitalize on the positive changes in the Chinese regulatory environment to expand the China innovation ecosystem. He built multiple successful partnerships that delivered new medicines to the China market including Innovent Biologics (sintilimab) and Chi-Med (fruquintinib). At Eli Lilly and Company he also initiated the project and led the team who delivered abemaciclib, the best in class cdk4/6 inhibitor, to the clinic.
His interests include discovering and developing medicines and the application of translational research principles to drug discovery. He was a co-founder and a member of the Board of Directors of the Asian Cancer Research Group, a not-for-profit company focused on the generation and dissemination of genetic and clinical data on cancers of importance in Asia. Dr. Blanchard received a BS degree in chemistry in 1977, a PhD in Biochemistry in 1982, and an MD in 1985 from Indiana University. He completed a residency in Internal Medicine and fellowships in Hematology and Medical Oncology at the Brigham and Women’s Hospital, the Dana Farber Cancer Institute, and Harvard Medical School in 1990. Dr. Blanchard was a Damon Runyon Fellow and a Fellow of the American Cancer Society. Prior to coming to Eli Lilly and Company in 2000, he was a tenured Professor of Medicine and Biochemistry & Molecular Biology at Louisiana State University Health Sciences Center in Shreveport, LA. He has had multiple global roles in Lilly Research Laboratories including Senior Clinical Research Physician in Program Phase Oncology, Chief Scientific Officer Cancer Discovery, Executive Director of Cancer Discovery & Lilly Systems Biology-Singapore, Chief Operating Officer/Vice-President of Discovery Research and Vice-President of Integrative Biology, and Vice-President of Tailored Therapeutics. He was a member of the board for Lilly China and Zymeworks INC and is a member of the board for The Confucius Institute in Indianapolis; he is also a member of the scientific advisory board for CBmed GmbH in Graz, Austria.
Dr. Qiu is the CEO of Qilu Regor Therapeutics, an innovative drug discovery company he founded together with a team of accomplished scientists and executives from top global pharma companies. Located in Shanghai, Boston and San Diego, Regor leverages world-class expertise in Computer Accelerated Rational Discovery (CARD) and efficient R&D ecosystems to accelerate the delivery of novel therapeutic agents with high unmet medical needs for patients in China and around the world.
Before returning to China in 2018, Dr. Qiu was Executive Director & Head of Structural & Molecular Sciences at Pfizer. He built and led a team of ~60 scientists with industry-leading expertise in structure-based drug design, computational sciences, and integrated molecular mode of action approaches. Prior to joining Pfizer in 2001, he was a member of GSK Global Target Evaluation Meeting and Novel Targets Committee. In 25 years in industry, he has contributed to 30 clinical candidates across diseases areas (inflammation & immunology, neurosciences, oncology, cardiovascular & metabolic, infectious & rare diseases) and therapeutic modalities (small molecule, ADC, biologics & vaccine). He discovered PCSK9 molecular mode of action that led to the industry-wide shift from seeking protease inhibitors to antibody therapies. He built the first cutting-edge cryo-EM lab in industry & New England, and delivered multiple clinical candidates using fragment-screening. He also served as President of New Drug Research for Qilu, one of the biggest pharmaceutical companies in China.
Dr. Qiu graduated from Peking University, obtained PhD at Michigan State, and completed executive trainings at Harvard Business School. He was an NIH Fellow and HHMI Research Associate at University of Washington in Seattle. He has trained 15 postdocs, served on expert review panels for National Institute of Health and other US funding agencies, and has been a member of Faculty of 1000 since 2004. He has >6000 citations (h-index 39) from over 60 publications, including in top journals such as Nature and Science.
Sr. Vice President and Head of Lilly China Drug Development & Medical Affairs Center (LCDDMAC) Eli Lilly
Education & Academic Career:
• Postdoctoral Research Follow,
Massachusetts General Hospital, Harvard Medical School
• M.D. ,Ph.D.
Shanghai Medical School, Fudan University
• June,2017 to present
Sr. Vice President, LCDDMAC, Eli Lilly China
• Sep, 2010 to June, 2017
Vice President in LCDDMAC, Eli Lilly China,
• Apr 2007 to Sep 2010
Oncology Medical Director of GlaxoSmithKline China/HK
• Sep. 2001 to Mar. 2007
Oncology Chief Clinical Research Physician, Eli Lilly China
Vice President and Head of MSD China R&D MSD Research Laboratories
Zhengqing Li is the Vice President and Head of MSD China R&D. In this position, he is responsible for the operation and strategic direction of MSD R&D Center in Beijing. As the China R&D head, Zhengqing leads a development team whose primary mission is to bring innovative medicines and vaccines effectively and efficiently to meet unmet medical needs of Chinese patients. In addition, Zhengqing plays the leadership role in building MSD global capabilities in China, and in establishing external collaborations with research institutes, professional societies and industry partners. Under his leadership over the past 8 years, the MSD China R&D Center has been growing dramatically with more than 1000 scientists with expertise across Clinical Research, Regulatory Affairs, Clinical Trial Operations, Pharmacovigilance, Project Management, Biostatistics, Epidemiology, and Data Management, etc.
Prior to joining MSD, Zhengqing took a number of leadership roles with Bristol-Myers Squibb (BMS) including the Head of Clinical Research, China R&D and Executive Director and Head of Oncology & Neuroscience, Global Biometric Sciences. Prior to joining BMS, Zhengqing also worked with Pfizer and Procter & Gamble Pharmaceutics with increasing responsibility in drug development.
Zhengqing has authored and co-authored more than 40 scientific and clinical trial methodology papers and abstracts. He has played leadership role in the development and approval of nearly 20 drugs in China and United States. Which including famous HPV vaccine GARDASIL and GARDASIL 9, chronic HCV drug ZEPATIER and key product of immunotherapy KEYTRUDA, etc.
Zhengqing was born and grew up in China. He received his undergraduate education at University of Science and Technology of China and his PhD degree from University of Wisconsin-Madison with major in Biostatistics. Upon completion of his PhD, Zhengqing took a faculty position in the School of Public Health at State University of New York.
Chief Medical Officer Elpiscience Biopharma
Dr. Chin’s career spans over 20 years of experience in medical oncology and clinical development in the pharmaceutical industry. In January 2020 he was appointed as CMO at Elpiscience Biopharma.
Prior to joining Elpiscience, Dr. Chin was a Senior Medical Director of immuno-oncology, Global Clinical Development at AstraZeneca. There, Dr. Chin provided leadership and expertise to enable new investment decisions in oncology therapeutic development, which involved the successful development of clinical strategy, determining the direction of regulatory interaction and coordination/execution of new clinical trials. Prior to his career at AstraZeneca, Dr. Chin was a Global GI Oncology Lead at Eli Lilly. He was involved in the transfer of cetuximab (Erbitux) full rights in North America from BMS to Lilly, led regulatory submission for Erbitux label updates, and fulfilled Erbitux post-marketing commitment.
Dr. Chin started his career as a medical oncologist and served as an assistant professor in the Division of Hematology/Oncology at the Medical University of South Carolina in Charleston. He was a clinical investigator with a special interest in cancer therapeutic development and correlative studies. Over his career, Dr. Chin has served as PI or Co-I in over 20 active clinical trials. He is currently a member of the executive committee for the Chinese American Hematology and Oncology Network, a non-profit organization focused on fostering exchange of medical information between United States and China in the fields of hematology and oncology.
Head of Clinical Developments
James Jin, MD & Ph.D. He is the Head of Clinical Development in Novartis China since Aug 2019. He got Bachelor of Clinical Medicine in Shanghai Medical University, and then Master& Ph.D of Urology, Huashan Hospital, Shanghai Medical School, Fudan University in 2003. He has about 7-year clinical practice experience in hospital before joining industry. He has more than 16-year working experience and taking leadership role in MNC Medical Dept. He joined Wyeth Pharm in 2003 as Medical Manager and then Boehringer Ingelheim Pharm as Head of Clinical Development & Medical Affairs in 2008. He joined Eli Lilly as Medical Director of Clinical Development & Medical Affairs in Bio-Medicine in 2012. He has experience in multi-therapeutic areas, such as immunology, CNS, anti-infection, urology, respiratory, CV, diabetes, ophthalmology and oncology et al.
President and Chief Scientist Genor BioPharma
Visiting Professor Peking University
Previously, Dr. Zhou was Scientific Director at Amgen, Thousand Oaks, USA. His over 20-years experience of process development, multiple project management capacity in cGMP and non-GMP reproducible purification/production of protein/antibody therapeutics from FIH to CPD with depth knowledge of CHO clone selection, cell culture optimization, real time analytical assays, formulation and product specification for drug substances and drug products made Dr. Zhou many times as Project Process Team Leader/Project Team Leader/Cross Functional Core Investigation Teams Leaders at Amgen in the past.
Dr. Zhou has proven bio-industrial leadership in scientific innovation and technology evaluation, and is well known for implementation of membrane chromatography in mAb large-scale processing. Dr. Zhou has excellent reputation and an extended external network in the Process Development and or Process science peer community due to his extensive speaking and publication record including research articles, patents and book chapters in the Process Development and Process science field. Dr. Zhou has proven records for design space for process robustness and viral clearance in mAb production. Dr. Zhou was awarded as 2007 Amgen’s “Excellence n Science and Engineering” for his major achievement and leadership on photo-oxidation on monoclonal antibody yellowing, and selected by Amgen as a visiting professor teaching the GMP Master’s Degree Program at PKU, People’s Republic of CHINA since 2007.
Maggie Gu (Juanhong) is Vice President – R&D Shanghai Innovation Hub at Ipsen, a leading biopharmaceutical group dedicated to improving lives through innovative medicines in oncology, neuroscience and rare diseases.
Maggie has over 20 years of experience in clinical development, Medical affairs and Clinical Research operations in pharmaceutical indursry. Prior to Ipsen, she was Vice Present – Clinical research and operatnions in Junshi Bioscience, where she led and contributed to regulatory approval of the first China-developed PD-1 anti-body.
She started her career in the pharmaceutical industry as a Clinical Research Associate in Daiichi in 1997, and worked through the roles as Clinical Research Project Manager in MSD, Medical affairs manager in Fujisawa, Head of Clinical Operations and Therapeutic Area Medical Science Director at GlaxoSmithKline, as well as the Senior Director-Clinical Development in Clinical Operations at AstraZeneca.
She has successfully led development and registration activities of a series of innovative products in Oncology, Dermatology, Respiratory and other areas in China, including Tuoyi, Tagrisso, Botox, Avodart, Protopic etc. Prior to joining the pharmaceutical industry, Maggie worked in the Pediatric Research Institute,
Children’s Hospital affiliated to Shanghai Medical University. She holds a Master‘s degree in Pediatric Medicine from The Shanghai Medical University.
Xiang Yang Zhu
Chief Executive Officer Huaota Biopharm and Huabo Biopharm
Dr. Zhuis an expertin antibody drug discovery and process developmentwith more than 18 yearsof industrial experience. Hehas extensive experience in antibody drug discovery, process development, and manufacture facility construction. Dr. Zhu is the CEO for both Huaota Biopharm and Huabo Biopharm (members of Huahai Pharm), leads its global biotherapeutic research.Prior to join Huahai, he worked at Boehringer Ingelheim for more than 8 years in different function areas at multiple locations (Ridgefield, USA; Biberach, Germany; and Shanghai, China). He led andengaged inover 20 global BI biological research projects including current clinic Phase I-III projects and market products; Dr. Zhu obtained his PhDin microbiology and immunology fromtheUniversity of Illinois at Chicagoand has authored more than 20 publications in peer-reviewed journals.
President, CMO and Board Director Adlai Nortye Biopharma
Dr. RuiRong Yuan is the President, Chief Medical Officer (CMO) and Board Director of Adlai Nortye Biopharma. She previously served as CMO & President of global clinical development at BeiGene; CMO and Vice President of Eisai Global Oncology, Head of multiple therapeutic areas at Daiichi Sankyo and senior global clinical leader at Novartis Oncology. Dr. Yuan has decades of successful drug development experience and played a critical leadership role in the development, regulatory approval and commercialization of multiple compounds, including anti-cancer drug Afinitor, Zelboraf, Lenvatinib, Halaven and anti-PD-1 and other IO molecule combination regimens. She has been a frequently invited speaker at national and international oncology meetings and has established strong collaborations with internationally recognized key opinion leaders to promote new drug development in oncology.
Dr. Yuan is an US-board certified medical oncologist and attending physician at VA Medical Center of New Jersey Medical School. She has had extensive academic clinical practice and research experience as a physician-scientist at top cancer centers in China, Switzerland and the US. She has published many peer-reviewed original research articles and holds multiple patents related to either cancer treatment or autoimmune disease therapy.
Dr. Yuan also remains actively involved in promoting cancer research collaborations between the hematology and oncology communities in the west and east worlds. She is one of the founding members of Chinese American Hematologist and Oncologist Network (CAHON) and served previously as its president and Board chair. She has been an executive member of the Chinese Society of Clinical Oncology (CSCO) since 2004 and served on the ASCO-International Affairs committee from July 2006 to June 2009. She also serves as editor for multiple Journals of hematology and Oncology. Dr. Yuan is the guest professor at Shandong University hospital and HeNan University Hospital, and vice chair of CSCO-COE (committee of overseas experts) to promote global cancer research collaboration and improve cancer care.
Chief Executive Officer and Chief Scientific Officer Denovo BioPharma
Dr. Wen Luo has over 20 years of experience in biomedical research and industry including more than 15 years of experience in applying genomic technology in drug discovery and development. Prior to founding Denovo Biopharma, Dr. Luo managed the genomic group and provided bioinformatic support to a broad range of research projects across a number of therapeutic areas including oncology, hematology, inflammation and metabolic diseases at Ligand Pharmaceuticals. He was also responsible for developing clinical biomarkers for drugs in various stages of clinical trials. Before joining Ligand, he was a senior scientist for bioinformatics at Incyte Genomics, where he managed one of the largest proteomic databases, LifePro. He was also involved in discovering novel human genes and splice variants, and was the co-inventor of patents covering hundreds of novel genes derived from these findings. Prior to Incyte Genomics, he was a research scientist at Sugen, which had been acquired by Pharmacia, where he worked on drug target identification and validation for a number of novel kinases discovered at Sugen. Dr. Luo was a Howard Hughes Medical Institute post-doc fellow at the University of California, San Francisco, and received his Ph.D. in Molecular Biology and Biochemistry from Indiana University School of Medicine. Dr. Luo received pre-med training at Peking University and medical training at Peking Union Medical College.
Chief Scientific Officer
Hequn Yin is currently CSO of Fosun Pharma. Prior to joining Fosun, Hequn was a VP of Pfizer Oncology R&D in California, USA. Before Pfizer, he spent nearly 20 years with Novartis in New Jersey, USA where he held positions of increasing responsibility from a Sr scientist to an Executive Director. Hequn also worked at Hoffmann-La Roche in New Jersey during 1997-98.
Hequn received a B.S. in chemistry from Peking (Beijing) University in 1985 and a M.S. from the Chinese Academy of Sciences in 1988. He earned a PhD degree in pharmacology from the University of Rochester, USA in 1995. Subsequently he conducted post-doctoral research in molecular biology & biochemistry at UC San Francisco, USA between 1995 and 1997. He also attend the eMBA program at Fairleigh Dickinson University in New Jersey.
SVP, Head of Business Development Zai Lab
Jonathan Wang is our head of business development since 2014. Prior to joining Zai Lab, Mr. Wang was an investment professional at OrbiMed, where he was responsible for China healthcare investment and portfolio management. From 2005 to 2011, Mr. Wang worked as a consultant at the Boston Consulting Group in China, where he specialized in pharmaceutical and healthcare engagements, assisting multinational and local companies with their China strategy. Previously, Mr. Wang also gained financial transactional experience at Goldman Sachs Investment Banking. Mr. Wang received a master of business administration in healthcare management from Wharton Business School.
Senior Director & Asia Emerging Science Lead (Shanghai), Asia Discovery Labs, Emerging Science & Innovation (ES&I)
Pfizer Worldwide Research & Development
Dr. Feng Bian is a Senior Director and Asia Emerging Science Lead in Pfizer Asia Discovery Labs (ADL) of Pfizer’s Worldwide Research and Development. She is responsible for cultivating strong and in-depth scientific relationships with Asia Academic and Life Science Communities with a primary focus on southern China regions to access emerging sciences, promising compounds, and breakthrough technologies.
Prior to ADL, Dr. Bian was a senior investigator in China Novartis Institutes for Biomedical Research and group head of liver pharmacology since 2014 in Shanghai. At Novartis, she was a project leader and managed liver disease pharmacology platform to deliver data packages for drug discovery projects. Before Novartis, she was a key scientist participated in setting up JnJ China research labs in 2012, and Associate Director of Biology to manage CROs and academic collaborations as well as internal R&D programs. Dr. Bian began her R&D career in Parke-Davis/Warner-Lambert in US as an in vivo pharmacologist in the Neuroscience Division, and later became a principle scientist in Pfizer’s Neurodegeneration and Psychotherapeutics Unit, contributing to programs like Lyrica®, discovery programs for Alzheimer’s disease, bipolar depression and dermal fibrosis. Dr. Bian has 20 years of expertise in small molecule and biologics drug discovery and her work has enabled NMEs to reach first in human. Dr. Bian received her Doctorate degree in Biochemistry from The Ohio State University and her Bachelor of Science degree from Nankai University at Tianjin, China.
Qun (Max) Dang
Corporate Vice President, President, CEO
CSPC, CSPC Shanghai Research Institute, InnovStone Therapeutics
Max received his BS from Jilin University with honors and earned a CGP national scholarship sponsored by the Chinese government; he obtained his Ph.D. in organic chemistry from Purdue University in 1992, joined Gensia (later became Metabasis) as a medicinal chemist and worked until 2009 with his last position as director of medicinal chemistry. Max then joined Merck as a Senior Investigator in the External Basic Research department, and then from 2011 to 2013, he was Director of External Medicinal Chemistry, Asia Lead, based in Shanghai facilitating Merck-CRO operations;
2013-2016, he was a Principle Scientist in the exploratory chemistry department at the Kenilworth site. In 2016 he joined Eli Lilly as Asia Head, BD and External Innovation for diabetes and CV research and worked until March 2018 before joining Qilu Pharmaceutical as VP, Global Head of BD and External Innovation with responsibilities for all BD and external collaborations globally including in-license, out-license and setting strategies for drug discovery and external collaborations. In June 2019, Max joined CSPC as corporate VP, President of CSPC Shanghai Research Institute, CEO of InnovStone Therapeutics, responsible for small molecule new drug discovery efforts. Max has extensive experiences in business development globally
and more than 25-years of experiences as a manager of drug discovery programs spanning from early (Target Selection and Validation, Lead Identification) to late (Lead Optimization and candidate selection) stages; led programs that advanced multiple compounds into human clinic trials (two completed Phase 2b POC studies); experiences in therapeutic areas including diabetes, dyslipidemia, hepatitis B and C, liver cancer, liver fibrosis,
anemia, viral and bacterial infections; extensive knowledge of Structure-based Drug Design, Medicinal Chemistry, Drug Delivery, Prodrugs, Liver targeting Strategies, Combinatorial, Heterocyclic and Nucleoside Chemistry; more than five years of managing drug discovery programs executed at various CROs. His research activities have led to 91 publications and 60 patents.
Head of External Innovation APAC, Biopharma, Global Research and Development, External Innovation Merck Serono (Beijing) Pharmaceutical R&D
Dr. Chen Chen (Michael) currently works as Head of External Innovation APAC for Merck KGaA. Michael leads collaborations with academic institutions and local pharmaceutical companies in China and APAC areas with alignment of Merck R&D focus and requirement. He encompasses scouting and evaluation of external opportunities including assets from discovery to clinical PoC stages, new drug target/biomarker findings, and novel discovery technologies, through open innovation, licensing, co-development, investment and other collaboration models. He is also responsible for Merck global BD activities in China/APAC regions including various internalization and externalization opportunities.
Michael received his bachelor’s degree in cell and molecular biology from University of Essex, a master’s degree in cancer immunotherapy from University of Nottingham and a PhD in Biochemistry from Imperial College London. Before joining Merck, he has been leading research projects at Spirogen Ltd./MedImmune in UK, and business development/investment activities at WuXi AppTec and ChemPartner.
Weiyi Zhang is currently the director, external innovation China and head of Research Beyond Borders China at Boehringer Ingelheim. She is responsible for setting up collaborations in China for research functions at BI. Weiyi gained her bachelor degree in Biology at Xiamen University in 2001. She joined international Max-Planck research school in chemical biology in 2003 and studied function of olfactory G-protein coupled receptor in non-olfactory tissues. She obtained her Ph.D in cell biology from Ruhr-University Bochum in 2007. Since 2008, Weiyi started postdoc training in functional study of orphan GPCRs in central neural system at both National Institute of Biological Sciences and the University of Hong Kong.
Before joining Boehringer Ingelheim, Weiyi has led a cell biology group at BioDuro-PPD in Beijing since 2009, focusing on cell-based assays and integrated early drug discovery programs for various pharmaceutical companies. Then she has led the monoclonal antibody research group at Bio-Rad Laboratory in Shanghai from 2012 to 2013. From 2013 to 2016, Weiyi was the associate director of Innovation Partnering at Innovation Center China of Global Drug Discovery at Bayer Healthcare.
BD & Licensing Manager
Roche Pharma Partnering
Dr. Dadong Li is currently a BD & Licensing Manager with Roche Pharma Partnering, based in Shanghai office. He is in charge of BD efforts in China across various therapeutic areas, from preclinical to late stage, and represent both Roche and Genentech. Prior to joining Roche, Dadong was a commercial officer with UK Department for International Trade at British Embassy in Beijing, where his responsibility is to facilitate UK China investment and trade in healthcare sector. Dadong also worked as a management consultant with PwC Management Consulting on strategy for healthcare companies and he has experience with Chinese Academy of Sciences as a junior scientist.
Dadong holds a Ph.D. in Chemistry from New York University, and a Bachelor degree in Materials Chemistry from Peking University.
Director, Search & Evaluation, JAPAC
Dr. Bin Li is currently Director, Search & Evaluation, JAPAC at AbbVie in Shanghai, responsible for search and evaluation of partnership opportunities in key therapeutic areas of immunology, oncology, neuroscience, and liver diseases. Prior to joining global S&E team in July 2015, he was site head of AbbVie China R&D Center in Shanghai which focuses on pre-clinical drug discovery in several therapeutic disease areas including chronic kidney diseases. Dr. Li joined Abbott R&D Center, Shanghai in September of 2008 to head the center and carry out drug discovery research in several key therapeutic areas, and continued to head the center following separation of pharmaceutical business and formation of AbbVie. Prior to Abbott, Dr. Li was Vice President, Service Biology at ChemPartner to build and lead the service biology division. Before returning to Shanghai, he spent 16 years in US pharmaceutical and biotech companies, including Roche, Pfizer, Anadys, and Xceptor, with various titles from Research Scientist to Director to lead and support drug discovery research as well as drug screening and lead discovery technologies such as ATLAS, an affinity-based high throughput screening platform for protein ligand identification. Dr. Li received his B.S. from Lanzhou University in China in 1982, M.S. from Iowa State University in 1986, and Ph.D. from Penn State University in 1990. Dr. Li has more than 25 years of drug discovery experience in various therapeutic disease areas.
Zhao-Kui (ZK) Wan
Fellow of the Royal Society of Chemistry, Founder & Chief Executive Officer
Dr. Wan is the founder and CEO of Lynk Pharmaceuticals, a VC supported biotech company focusing on oncology, auto-immune and inflammatory diseases. Dr. Wan earned his Ph.D. degree from Boston University, then conducted a postdoctoral research at Harvard University. Before starting Lynk Pharmaceuticals, Dr. Wan served as the Head of Chemistry at JNJ’s Asian Pacific Discovery Center with various cross-function responsibilities. He was one of the key leaders and played an instrumental role of building the Center from its earliest inception. Prior to JNJ, Dr. Wan had worked for Wyeth/later Pfizer for a dozen years and served as a group & project leader as well as a postdoc research advisor.
Dr. Wan has research experiences in multiple therapeutic areas and made significant contributions to the development a number preclinical candidates, clinical compounds and marketed products. Dr. Wan has more than 50 scientific publications in peer-reviewed journals and meeting abstracts; he also has close to 140 world and national patents. Dr. Wan won a number of awards and recognitions; he is an elected Fellow of the Royal Society of the Chemistry (2015), a winner of Young Industrial Investigators Award (ACS, 2008) and a steering committee member of Chemistry in Cancer Research of AACR (2017). Dr. Wan is a co-founder & a member of Board of Directors of Chinese BioMedical Association (CABA) and served as the President (2009- 2010). He is also a member of many prestigious professional organizations such as AACR, BayHelix and ACS.
Head Patents China
Novartis Pharmaceuticals ( China )
Head Patents China, Novartis Pharmaceuticals (China)
Kent Yang joined Novartis Pharma China as a Patent Attorney in 2012. He is now heading the China Patent Team, providing patent and other IP supports to all local business units and franchises of Novartis Pharma and Novartis Oncology in China. His team’s responsibilities range from patent matters such as patent prosecution, invalidation, infringement, and due diligences, to other IP areas such as technical trade secret disputes, regulatory data protection, name creation and trademarks, copyright, and etc.
Before joining Novartis, Kent was a patent attorney with the Shanghai-based patent firm Shanghai Patent and Trademark Law Office for 7 years.
Kent is a qualified patent agent in China, and holds a bachelor degree in Biology and a master degree in Tumor Pharmacology
VP Patent China
Roche Group Patents
Frank Zhu is VP Patent China, Roche Group Patents. In his current role, he is responsible for Roche’s IP affairs in China. He and his team provides IP support to all Roche’s affiliates in Greater China. Before joining patent department, Frank Zhu was project manager and portfolio manager at Roche Innovation Center Shanghai. Before joining Roche in 2004, he was an engineer at Shanghai R&D Center for Polymer Materials. He graduated from Donghua University in 2001 with a master’s degree in polymer materials. He is a member of Patent Leadership Team of the Roche Group.
Chief IP Officer
3S Pharmaceutical Group
Li Caihui is Patent Attorney\ Senior Engineer\Licensed Pharmacist
√ Sept. 1988-July 1992, Bachelor, Department of Pharmacy, Shenyang College of Pharmacy
√ Aug.-Oct. 1993, Synthesis of peptides Beijing Medical University
√ Feb. 2002, Training on IPRs AOTS training center( Tokyo Japan)
√ 30 cases of patent invalidation /administrative petition with MNC on antibody medicine in China
√ Invalidation on ZL20061008639.X is honored as one of 10 national cases on patents reexamination and invalidation in 2014
√ 2016 Shanghai Labor Medal
Vice President, Analytical Operation Huahai Pharmaceutical
Dr. Min Li received his PhD in Organic Chemistry from Johns Hopkins University in 1991. Following a postdoctoral research in medicinal chemistry, he had worked for several multinational pharmaceutical companies with increasing responsibilities, including Roche, Merck & Co., Inc. Schering-Plough, and Merck again. Over the years, he has led technical teams of senior-level scientists for various analytical and pharmaceutical manufacturing process investigations and troubleshooting, impurity peak identification, study of drug degradation chemistry, analytical development, and support for new drug filing. Since September 2014, he became Vice President for Analytical Operation at Huahai Pharmaceutical, a leading Chinese pharmaceutical company with operations in both China and US. He also established the Center of Excellence for Modern Analytical Technologies (CEMAT), a technical core group created for solving the most challenging technical problems from pharmaceutical R&D to scale-up and commercial production at the company.
Dr. Li is a leading expert in drug degradation chemistry and he published a single-authored book, “Organic Chemistry of Drug Degradation” (by Royal Society of Chemistry) in 2012; the Chinese translation of this book was published in September 2019. He is the first/communicating author of more than 50 publications in organic, medicinal, bioconjugate, and analytical chemistry (including mass spectrometry). He is currently a member of the expert committee (Chemical Medicines 5) at United States Pharmacopoeia (USP) and a board member of Sino-American Pharmaceutical Professional Association (SAPA).
President & COO, Co-Founder Ascentage Pharma
Dr. Guo has been working in the healthcare industry since 1991, including ABC Laboratories, Pfizer, Ascenta Therapeutics, and Ascentage Pharma. At Pfizer (1995-2005) with various technical and management roles, Dr. Guo participated in many NCE drug R&D projects, several of which have successfully reached commercial stages. At Ascenta (2005-2009), Dr. Guo was the founding Vice President of Pharmaceutical Sciences & Manufacturing, and also General Manager of Ascenta (Shanghai) R&D Center which engaged in NCE drug R&D in China from 2005. Dr. Guo played an important role in Ascenta’s >$600M global out-licensing deals (i.e., with Sanofi-Aventis in 2010 and with Debio in 2011). Dr. Guo co-founded Ascentage Pharma in 2009, a globally positioned China innovative NCE drug R&D company, and currently serves as President & COO. The company has quickly built up a pipeline of 8 clinical-stage NCE projects along with several IND-enabling and discovery stage projects, covering oncology and anti-aging / anti-viral therapeutic areas through its apoptosis/PPI platform. During 2002-2005, Dr. Guo served as an Overseas Advisor for Beijing Zhongguangcun Biotech Park in China. He has been an adjunct professor, a faculty and graduate student adviser for the IPEM program at Peking University during 2007-2018. Dr. Guo served as an Independent Board Director at Porton Corporation (Chongqing, China) during 2012-2016, overseeing its successful IPO at Shengzhen Exchange, China, in 2014. As a co-founder and the founding Chairman, Dr. Guo has served on Board of Directors of SABPA (www.sabpa.org). Dr. Guo received his Ph.D. degree in Organic Chemistry at the University of California at San Diego; M.Sc. in Medicinal Chemistry at Institute of Materia Medica, Chinese Academy of Sciences; and B.S. in Chemistry at Peking Normal University.
Dr. Deepak Hegde completed his Doctorate in Biopharmaceutics and Pharmacokinetics from University of Mumbai in 1996. He also completed his Masters in Financial Management (M.F.M) from University of Mumbai in 2000.
He is currently working with EOC Pharma as Senior Vice President-CMC. Responsible for development and manufacturing of new speciality anti cancer products for China. Prior to joining EOC, he was with GSK Shanghai, R & D China as Director, Global External Development & Supply, AsiaPacific, responsible for developing drug products for GSK global portfolio and for introduction of new products to China. Prior to this he worked with Wuxi AppTec as Vice President for Formulation Development. At WuXi Apptec, he was instrumental in setting up the Formulation Development Business as well as the formulation team, GMP facilities and systems which have since been approved by the EMA, USFDA and CFDA. While working with several multinational companies from US and Europe, he helped develop more than 150 NCE’s. He established several enabling technologies like Microdozing, Nanonization, Spray Drying, and Holt Melt Extrusion (HME) etc. at WuXi AppTec which helped customers expedite the First in Man (FIM) studies in US, Europe, Australia, Korea & China. Prior to joining WuXi AppTec in Shanghai, he has worked at several positions across Rhone Poulenc, Sandoz (A Novartis Group Company) and USV Ltd, a premier Indian Generic Company.
He has extensive experience in generic formulation development of solid and liquid oral and injectible formulations from a very early phase of development all the way to technical transfers to commercial manufacturing sites. At Sandoz, he worked on formulation development for the regulated markets like US and Europe and participated in technical transfers to commercial sites of Sandoz at Rolab in South Africa, and Novartis Bangladesh and Novartis Pakistan. Several generic products that he developed have since been registered and commercially launched in Europe, USA, South Africa and Asia.
He is a life member of the Indian Pharmaceutical Association. He has two US patents, five PCT and US patent applications and several National and International publications to his credit.
Dr Dhileep Krishnamurthy is a senior pharmaceutical industry leader and have been advising and consulting in pharmaceutical research, development and technology platform for academia, industry and government across the world and in particular India, China and USA. Currently he is a CSO of NHU, China and working closely with government and Industry to enhance China and India collaboration in pharma industry.
For past 25 years, Dr Krishnamurthy has worked in various multinational organization including BMS, Boehringer-Ingelheim, Dr Reddys, Piramal and NHU with increasing responsibility from Scientist to VP, Global Head R&D and CSO in USA, Germany, India and China. His strengths include, (a) building, mentoring, strengthening innovator and generic business using the 4 pilar model. (b) Cost reduction in API manufacturing using R&D, technologies, manufacturing excellence including US FDA approved plants, (c) Efficient R&D development for DMF filing using competitive advantaged routes by GCbD and QbD.
He has obtained PhD in Chemistry from University of Utah, Salt Lake City and M.Sc from IIT, Bombay. He has more than 100 publications, patents and invited presentations to his credit. He has co-invented commercial process new drug Entacavir and Empagliflozin when he was working in BMS and BI. Recently, he has been named as Fellow of Royal Society of Chemistry and member of National 1000 talent program from PR of China. He also won the highest award for a foriegner “West lake friendship award” from Zhejiang Province, China. He served as one of the panel judges in “Presidential Green Chemistry Challenge Award” EPA, US Government and currently he is an editorial advisory board member in Green Chemistry a RSC Journal based in UK
Senior Vice President, CMC Shenogen Pharma Group
After Obtained his Ph.D. from Purdue University, Dr. Chen joined Department of Process R&D in Gilead Sciences Inc., and was responsible for process optimization, tech transfer and commercial manufacturing. He participated in many Gilead’s blockbuster projects, such as Viread, Emtriva, Hepsera, Truvada and Atripla. The combined sales of these products in 2012 exceeded 35 billion dollars.
Starting from 2009, Dr. Chen held several executive positions for some pharmaceutical companies, including Process Director in WuXi AppTec Co., Ltd., Vice President of API division in Huahai Pharmaceutical Co., Ltd., Executive Vice President in Tibet Rhodiola Pharmaceutical Holding Co., President in Zhongke Biopharma Co., Ltd. Dr. Chen has 22 years pharmaceutical experiences in USA and China. His specialty is in areas of CMC and drug substance manufacturing. He has managed a wide range of projects, including API manufacturing, GMP appliances, formulation development, facility construction and supply chain management.
Vice President, Discovery and Early development Antengene
Vice President and CMC Head Dizal Pharmaceutical
Shih-Ying joined Dizal at January 2019 as the CMC head for API and drug products development, Clinical manufacturing, and supply chain management. Before coming back to Shanghai, he has worked in Pharmaceutical Development in Bristol-Myers Squibb at New Brunswick New Jersey for 13 years. During the tenure in BMS, he has worked on more than 40 different new chemical entities including Brivanib and Cabozentinib in the oncology area, contributed more than 5 NDA dossiers preparation, especially as the author of the Module 3 QbD sections for Onglyza, which was approved as the first QbD-based NDA filings. Other approved NDAs that he has participated including Sprycel, Kombiglyza, Reyataz, and Daclatasvir. After coming back to Shanghai to join Hutchison MediPharma as the Executive Director of Formulation at 2015, he has contributed to Fruquintinib NDA approval in CFDA. He has also served as the CMC project lead to collaborate with AstraZeneca for the joint global development of Savolitib. In Hutchison he successfully finished two bio-equivalency studies to facilitate formulation changes during pivotal trials.
Senior Vice President, CMC Hua Medicine
Dr. Jin She is SVP of CMC at Hua Medicine (Shanghai) Ltd. Dr. She has over 15 years’ of experience in the biotechnology and pharmaceutical industry. Prior to Hua Medicine, he worked at MSD R&D Center (China) as Director of Process Chemistry, and Roche R&D Center (China) as Head of Process Research & Synthesis. Before returning back to China from the US, he worked at Inspire Pharmaceuticals Inc. as Sr. Research Scientist and team leader of Process Research. Dr. She has also been an Industrial Advisor for Engineering Master Program at East China Science & Technology University for the last 8 years. Dr. She Received his Ph.D. in organic chemistry from the University of North Carolina at Chapel Hill. He obtained his BS and MS degrees in chemistry from Beijing University.
Vice President, Head of CMC Laekna Therapeutics
Dr. Feng is currently Vice President and head of CMC of Laekna Therapeutics. He oversees CMC development and manufacturing for all Laekna’s pipeline products. Dr. Feng has more than sixteen years’ experience in new drug research and development including preclinical development, early phase and late phase product development, clinical manufacturing and process validation towards commercialization. He has led the technical transfer, clinical manufacturing, and process validation of various products, including successful approval and commercial launch of Niraparib in China. Prior to Laekna, Dr. Feng has held various management roles in Zai Lab, WuXi Apptec, and Schering Plough in US. Dr. Feng received his PhD from Purdue University.