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Inspired by the human element to advance cell therapy


Determined to deliver what's

Legend About
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Learn more about the people and values that drive us forward


Mission / Vision / Values/ Code
Mission / Vision / Values / Code
Leadership Team
Leadership Team
Partnerships
Partnerships
Careers
Careers

Mission, vision, values and code—the principles we live by



Close up image of scientist examining a sample

Our Mission - The pursuit of a cure

Dedicated to quality and driven by excellence, we are committed to improving the lives of patients worldwide. We are steadfast in our goal to develop innovative cellular therapies that bring us closer to a cure.

From the very beginning, we’ve been focused on science. We came together as a team of experts dedicated to quality, driven by excellence, and committed to experimentation. Though we faced many challenges, we remain fearless in our research and rigorous in our thinking, pushing ourselves to work harder.

At Legend Biotech, we have the opportunity to change the way treatments are developed across diseases and continents. Our goal is to reinvigorate treatment approaches in oncology and beyond.

The spark of hope is lit and we’re using that hope to ignite the future of cell therapy!

Image of a cell

Our Vision - Igniting the future of cell therapy

We welcome the opportunity to reinvigorate the treatment approaches in oncology and the future of cell therapy.

Today, our research is focused on continuous innovation in the field of cell therapy. We are also future-focused on emerging technologies that can help address some of the most chronic and life-threatening diseases.

Our goal is to reimagine healthcare and to deliver transformative treatments.

And at Legend Biotech, that’s what we’re doing every day.

Image of grandfather and granddaughter smiling

Our Values - Sharing our passion with the world

Our driving force at Legend Biotech is sharing our passion for developing cutting-edge cell therapies with our colleagues and the healthcare community. We do that through:

Patient First: We keep patients at the forefront of our work.

Integrity: We value honesty, ethical business conduct and transparency.

Innovation: We promote a creative culture to drive scientific breakthroughs and continuous improvement.

Accountability: We deliver on our commitments.

Passion: We approach our work with dedication and enthusiasm.

Collaboration: We embrace differences, communicate openly and build trust.

Core Value image hands

Our Code - Our commitment to do the right thing

At Legend, we are striving to make a difference in health care, to improve the lives of patients, and to build sustainable value for our stockholders. Achieving these goals depends largely on our commitment to conducting business ethically. For more information, please review our Code of Conduct.

Our Code: is a summary of ethical and compliance principles that guide the company’s operations and employees. For more information, please review our Code of Conduct.

Executive Discussion

Compliance Program - Our commitment to compliance

Legend Biotech maintains a comprehensive compliance program to foster compliance with the laws, industry guidelines and company standards. Legend Biotech’s Comprehensive Compliance Program has been developed in accordance with the California Health and Safety Code § 119400 and 119402, and represents a good faith understanding of the regulation.

Read about our Comprehensive Compliance Program.

For questions about our Compliance Program, please contact compliance@legendbiotech.com.

Our leadership team brings extensive experience in developing cell therapies

Global Leadership Team

Ying Huang
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Ying Huang, PhD

Chief Executive Officer, Legend Biotech.
Chief Financial Officer, Legend Biotech.

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Ying Huang

Ying Huang, PhD

Chief Executive Officer, Legend Biotech.
Chief Financial Officer, Legend Biotech.

Dr Huang has served as Chief Financial Officer since July, 2019. He brings over 9 years of experience in research and development at major multi-national pharmaceutical companies and 12 years of experience as a biotechnology analyst on Wall Street.

Most recently, Dr Huang was a Managing Director and Head of Biotech Equity Research at Bank of America Merrill Lynch where he led a team of analysts covering more than 30 biotechnology companies including Amgen, Gilead, Celgene, Biogen and others that encompass a wide range of therapeutic areas. His knowledge and expertise have been recognized by the Institutional Investor survey as a top ranked biotechnology analyst on Wall Street. Dr Huang has been a biotech analyst since 2007 and previously worked at Wells Fargo (formerly Wachovia), Credit Suisse, Gleacher and Barclays before joining Bank of America Merrill Lynch. Besides providing investment research to investors, Dr. Huang and his team conducted due diligence for numerous successful initial public offerings (IPOs) and follow-on offerings in the biotechnology sector.

Prior to his Wall Street career, Dr Huang was a Principal Scientist at Schering-Plough (now Merck & Co.) in the Department of Chemical Research focusing on small molecule drug discovery in the therapeutic areas of cardiovascular and central nervous system. He is the co-author of multiple patents and peer reviewed publications. Dr Huang received his Doctor of Philosophy in Bio-organic Chemistry from Columbia University, New York, USA. He also studied in the Special Class for the Gifted Young at the University of Science and Technology of China and Columbia Business School.

Frank Fan
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Frank Fan, MD, PhD

Co-Founder & Chief Scientific Officer

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Frank Fan

Frank Fan, MD, PhD

Co-Founder & Chief Scientific Officer

Dr Fan is a co-founder of Legend Biotech and its Chief Scientific Officer since 2014. Dr Fan has been published in numerous peer-reviewed academic journals, including a major revision in the clinical guidelines of pediatric organ transplantation published in Nature Medicine. Dr Fan was also awarded a “New Key Opinion Leader” award by The International Society of Transplantation.

Dr Fan earned his Doctor of Medicine degree at Xi’an Jiaotong University, China, and completed his surgical residency at the Jiaotong University Kidney Transplant Center, China. Dr Fan later obtained his Doctor of Philosophy in applied immunology at Hiroshima University, Japan, and completed postdoctoral training in the field of human B-cell tolerance at the Hospital for Sick Children at the University of Toronto, Canada.

Meeta Chatterjee
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Meeta Chatterjee, PhD

Senior Vice President, Global Business Development

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Meeta Chatterjee

Meeta Chatterjee, PhD

Senior Vice President, Global Business Development

Dr Meeta Chatterjee has served as the Senior Vice President of Global Business Development since March, 2019. She was previously Head of Strategy, Transactions, and Operations within the Business Development and Licensing (BD&L) group at Merck Research Labs. Dr Chatterjee oversaw discovery and late-stage transactions worldwide, as well as early-stage transactions in key geographies. She also was responsible for Merck’s BD&L governance, oversight, and control as well as out-licensing efforts.

Dr Chatterjee has over 30 years of broad strategic and operational experience in pharmaceutical research and development, mergers and acquisition evaluation, in-licensing, and externalization activities. Over the course of her extensive career, she has led/contributed to >150 transactions/collaborations with a cumulative financial value of ~$1 billion USD. She has led research efforts in the areas of hypertension, atherosclerosis, and obesity, and was an integral contributor to the discovery of ZETIA and ZONTIVITY.

Dr Chatterjee received her undergraduate education at St. Xavier’s University in Ahmedabad, India, and Rutgers University (B.A., Hons Physics), New Jersey, USA. She received her Doctor of Philosophy in Physiology from Rutgers University and completed a postdoctoral fellowship in the Department of Physiology at the University of Virginia, School of Medicine, Virginia, USA. Dr Chatterjee is also active in industry and licensing focused organizations.

Tracy Luo
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Tracy Luo, MD

Vice President, Clinical Development

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Tracy Luo

Tracy Luo, MD

Vice President, Clinical Development

Dr Tracy Luo has served as Vice President of Clinical Development, Greater China, since May, 2018. Dr Luo has a comprehensive understanding of the Chinese regulatory environment and dynamics and has more than 15 years of experience advancing clinical development programs in the oncology and hematology therapeutic areas. Previously, Dr Luo led multiple global oncology and hematology products through the clinical development stage at AstraZeneca, Amgen, and Sanofi. Her efforts led to numerous successful regulatory filings and commercial launches, including IRESSA, FASLODEX, BLINCYTO, KYPROLIS, and ELOXATIN. Previously, Dr Luo spent more than 6 years as a pharmacology research scientist at Fudan University Shanghai Medical School, China.

Dr Luo earned her Doctor of Medicine degree from Qingdao Medical College, China, and a Master of Science degree in pharmacology at Fudan University, China.

Steve Gavel
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Steve Gavel

Vice President, Commercial Development

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Steve Gavel

Steve Gavel

Vice President, Commercial Development

Mr Steve Gavel has served as Vice President of Commercial Development since July, 2018. He brings over 28 years of commercial experience in biotech start-ups, leading pharmaceutical and medical device organizations.

Most recently, Mr Gavel worked at Celgene Corporation, where he led US CAR-T commercial development activities for their bb2121 program. In this role, he led commercial launch strategy and execution planning in the United States. Prior to Celgene, Mr Gavel led VELCADE marketing strategy and execution at Takeda Oncology, where he served as Senior Marketing Director.

Prior to Takeda Oncology, Mr Gavel held multiple sales, marketing and market access leadership positions in companies such as Syntex, Immunex, Johnson & Johnson, and IMS Health.

Mr Gavel earned his Bachelor of Science degree in finance and business administration from Millersville University in Millersville, Pennsylvania, USA.

Chong Yang
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Chong Yang

Vice President, Commercial Development

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Chong Yang

Chong Yang

Vice President, Commercial Development

Mr Chong Yang has served as Vice President of Commercial Development, Greater China since July, 2018. Formerly, Mr Yang held various sales and marketing leadership roles with increasing responsibilities in multinational pharmaceutical companies including Roche Oncology, Bayer Oncology, and Novartis Oncology. He brings more than 17 years of commercial experience and has extensive expertise in promoting and launching products including GLIVEC, NEXAVAR, AVASTIN, and RITUXAN in the China market.

Mr Yang earned his Master of Medicine degree from Nanjing University, China, and served as a Surgical Resident at Zhongda Hospital at Southeast University, China.

Liz Gosen
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Liz Gosen

Senior Vice President, Global Technical Operations

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Liz Gosen

Liz Gosen

Senior Vice President, Global Technical Operations

Ms Liz Gosen has served as Senior Vice President, Global Technical Operations since May, 2019. Prior to joining Legend Biotech, she was Vice President of Biologics Operations at Eli Lilly where she was responsible for the manufacturing, warehouse, and supply chain organizations for a 2-suite multi-product commercial and clinical monoclonal antibody (mAb) manufacturing facility.

During her 25-year career she has developed a broad experience in biotechnology manufacturing operations through assignments in the following areas: multiple large-scale manufacturing facility capital design/builds and start-ups, process engineering support and management, facility and utilities management, site process technology transfers, and successful process validation as well as operations, logistics, and validation management.

Ms Gosen has international commercial scale manufacturing experience as a Business Unit Leader of an Eli Lilly large-scale mAb facility in Ireland. She was responsible for the organizational build and development of the operations organization from the commissioning and qualification support phase through to FDA approval and commercial operations. Ms Gosen has extensive global regulatory inspection experience and has been directly involved in the worldwide regulatory submission, pre-approval inspection, and launch of five biologics products.

Ms Gosen holds a Bachelor of Science Degree in Materials Science & Engineering with a minor in Biology from Lehigh University, Pennsylvania, USA, and an MBA of Finance from Seton Hall University, New Jersey, USA.

Simon Wu
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Shu (Simon) Wu

Vice President, Operations- Research & Development Institute II

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Simon Wu

Shu (Simon) Wu

Vice President, Operations- Research & Development Institute II

Mr Shu (Simon) Wu has served as Vice President of Operations, Research & Development Institute II, since October, 2017. Formerly, Mr Wu was the Vice President of Operations for the Discovery Biology Business Unit at GenScript Inc., leading antibody therapeutics discovery and operations activities. Mr Wu is the co-inventor of 15 patents in the field of immunotherapy and has more than 10 years of therapeutic antibody discovery and development, organizational capability building, and management experience. He has contributed to the development of successful novel discovery platforms and has led many antibody and chimeric antigen receptor T-cell (CAR-T) candidates into clinical development.

Mr Wu received his Master of Science degree in molecular biology from the Chinese Academy of Science, China, and a Bachelor of Arts degree in microbiology from Nanjing Agriculture University, China.

Alan Kick
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Alan Kick

Vice President, Global Quality

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Alan Kick

Alan Kick

Vice President, Global Quality

Mr Alan Kick has served as Vice President of Global Quality since August, 2018. Prior to joining Legend Biotech, Mr Kick was Executive Director of Quality Operations at Celgene Corporation, responsible for the Global External Quality, Cell Therapy Quality, and Global Quality Supply Chain organizations. He previously held positions of increasing responsibility at Dendreon, Wyeth, Johnson & Johnson, and Hoffmann-La Roche. Mr Kick has nearly 30 years of experience in the pharmaceutical industry, including solid oral dosage, semi-solids, biologics, vaccines, sterile lyophilized products, cellular therapies, active pharmaceutical ingredient (API), commercialization, development, and laboratory management.

Mr Kick received a Bachelor of Science degree in biology from The College of New Jersey in Ewing, New Jersey, USA, and a Master of Science degree in business management from New Jersey Institute of Technology in Newark, New Jersey, USA.

Yuhong Qiu
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Yuhong Qiu, PhD

Vice President, Global Regulatory Affairs

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Yuhong Qiu

Yuhong Qiu, PhD

Vice President, Global Regulatory Affairs

Dr Yuhong Qiu has served as Vice President of Global Regulatory Affairs since May, 2018. Previously, Dr Qiu served as Executive Director of Regulatory Affairs at Novartis Oncology, where she worked for 12 years with increasing responsibilities. She has broad regulatory expertise spanning across both small and large molecule (biologics) development. Dr Qiu has led numerous successful global regulatory filings from first-to-human studies to marketing authorization applications. Before joining Novartis Oncology, Dr Qiu worked for 8 years at Johnson & Johnson, where she led a team of scientists in drug discovery and gained rich experience in drug candidate selection and characterization and preparation of nonclinical documents for first-in-human studies.

Dr Qiu received her Doctor of Philosophy degree and completed her postdoctoral training from the Baylor College of Medicine in Houston, Texas, USA. She received her Bachelor of Science degree in biochemistry from Wuhan University, China. Dr Qiu has authored or co-authored more than 30 publications in peer-reviewed journals.

Lida Pacaud
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Lida Pacaud, MD

Vice President, Clinical Development

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Lida Pacaud

Lida Pacaud, MD

Vice President, Clinical Development

Dr. Lida Pacaud joined Legend Biotech as the Vice President of Clinical Development in January, 2021. Most recently, Lida served as the Global Clinical Program Head and Executive Medical Director in Cell & Gene unit at Novartis. Prior to that, Lida worked at Roche and Wyeth. She has been the Medical Lead on several Phase I, II & III trials, including 3 major regulatory submissions to the FDA, EMA and other worldwide health authorities for KYMRIAH®, AFINITOR® and AVASTIN®. Lida has covered programs in breast cancer, brain tumors, sarcomas, Gastrointestinal and lung neuroendocrine tumors, diffuse large B-cell lymphoma, follicular lymphoma, and acute lymphoblastic leukemia. In her role in Cell & Gene unit in Novartis, Lida led clinical development and filling of KYMRIAH, first approved CART therapy worldwide that was also awarded the esteemed Prix Galien USA Award for Best Biotechnology Product in 2018. On this program, Lida led US breakthrough therapy designation and EU PRIME designation for DLBCL, as well as Regenerative Medicine Advanced Therapy (RMAT) designation for follicular lymphoma, and she oversaw large global cross-functional clinical teams up to 100 individuals. Lida has also experience in BD&L activities as clinical evaluator of external cell therapy opportunities.

Dr. Lida Pacaud holds a Doctor of Medicine degree and certification in Pediatrics from Tbilisi State Medical University and has trained in Pediatric Oncology and hematology in France.

Lori Macomber
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Lori Macomber

Vice President, Finance

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Lori Macomber

Lori Macomber

Vice President, Finance

Lori Macomber has served as Vice President of Finance since March, 2021. Prior to joining Legend Biotech, she held various financial positions within the life science industry, including experience in external and internal auditing, financial planning and analysis and controllership at Pharmacia, Eli Lilly, and AMETEK as well as privately held consulting company Kromite. Ms. Macomber holds a Bachelor of Science in Accounting from Pennsylvania State University and is a Certified Public Accountant.

Dong Geng
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Dong Geng, PhD

Vice President, Early-stage Drug Development

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Dong Geng

Dong Geng, PhD

Vice President, Early-stage Drug Development

Dr. Dong Geng joined Legend Biotech in 2018. Since then, Dr. Geng has taken increasing responsibilities primarily in Legend’s R&D portfolio development. She is responsible for non-clinical safety, pre-clinical and clinical pharmacology and translational sciences. Dr. Geng brought more than 22 years of biopharma industry experience to Legend. Prior to joining Legend, Dr. Geng had worked in leading biotech and pharmaceutical companies including Johnson and Johnson, BMS, Regeneron, Eli Lilly, and Merck. She has extensive experience in translational development of biologics especially immune-oncology therapies. During her career she has contributed and led numerous IND submissions and at least 7 successful BLA filings.

Dong received her Ph.D. in Biochemistry from Boston College.

Board of Directors

Sally Wang
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Sally Wang, MS

Board Chairwoman, Legend Biotech
President, GenScript Inc.

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Sally Wang

Sally Wang, MS

Board Chairwoman, Legend Biotech
President, GenScript Inc.

Ms Wang is the President of GenScript Inc. and a board Chairwoman for Legend Biotech Corporation, responsible for the companies’ strategies and overall operational management. Prior to joining the organization, she worked as an Environmental Monitoring Engineer at Shenzhen Futian Environment Protection Surveillance Station for nearly a decade.

Ms Wang holds several advanced degrees, including a Master of Science degree from Wuhan University, China, in August 1993; a Master’s degree in Computer Sciences from Bridgeport University in Bridgeport, Connecticut, USA; and an Executive Master of Business Administration degree from the China Europe International Business School, China.

Zhu Li
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Zhu Li, PhD

Board Member, Legend Biotech

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Zhu Li

Zhu Li, PhD

Board Member, Legend Biotech

Dr. Zhu served as the vice president of strategy of Genscript Biotech Corporation (“GenScript”) from March 2010 to February 2017, served as the chief strategy officer of GenScript from February 2017 to July 2019, and has served as a consultant for GenScript since July 2019. Upon his appointment as executive director of GenScript on November 22, 2020, he resumed his role as the chief strategy officer of GenScript. Before joining GenScript, Dr. Zhu worked at California-based Clontech Laboratories, Inc. as a director of molecular biology from January 1990 to March 2000. Dr. Zhu founded Genetastix Corporation, Inc., a biotech company focused on yeast-based antibody discovery, and served as president and chief executive officer from May 2000 to December 2005. Dr. Zhu then worked at biotech companies in China, serving as vice president of research at Cathay Biotech, Inc. from July 2006 to December 2008, and as vice president of HUYA Biomedical Technology (Shanghai) Co., Limited from January 2009 to December 2009. Dr. Zhu obtained a Bachelor of Science of Biology degree from the East China Normal University in February 1982 and a Doctor of Philosophy in molecular biology and immunology from Stanford University in July 1989.

Corsee Sanders
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Corazon (Corsee) Dating Sanders, PhD

Board Member, Legend Biotech
Board Member, Molecular Templates
Board Member, AbGenomics

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Corsee Sanders

Corazon (Corsee) Dating Sanders, PhD

Board Member, Legend Biotech
Board Member, Molecular Templates
Board Member, AbGenomics

Dr. Sanders has served on the board of directors at Legend Biotech since May 2020. Dr. Sanders has also been a member of the board of directors at Molecular Templates, Inc. since December 2019 and at AbGenomics since March 2020.

Dr. Sanders previously served as the Strategic Advisor to the Office of the Celgene Chief Medical Officer from March 2018 to November 2019. Her responsibilities included ensuring effective integration of Juno’s Development Organization into the Celgene Organization, specifically the unique chimeric antigen receptor T-cell (CAR-T) aspects, advising the label-enabling CAR-T legacy Juno program (JCAR017), and advising the Chief Medical Officer and his leadership team on evolving the clinical development organization.

Prior to her role as Strategic Advisor, Dr. Sanders was a Member of the Juno Therapeutics Executive Committee as Executive Vice President of Development Operations, with responsibilities for strategic operations, quantitative sciences, biosample and clinical operations from January 2017 to March 2018.

Dr. Sanders was a Member of the Genentech/Roche Late Stage Portfolio Committee from 2009 to 2017, and Global Head of the Genentech/Roche Late Stage Clinical Operations from 2012 to 2017, with responsibility for leading employees in planning and conducting global development and local clinical trials in over 70 countries.

Dr. Sanders has directly contributed and/or provided oversight in developing multiple pharmaceutical products, including a CAR-T cell therapy for Non-Hodgkin lymphoma.

Dr. Sanders holds a Bachelor of Science and a Master of Science in statistics, graduating Magna Cum Laude from the University of the Philippines, Philippines. She also received a Master of Arts and a Doctor in Philosophy in statistics from the Wharton Doctoral Program at the University of Pennsylvania, USA.

Darren Ji
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Darren Ji, MD, PhD and MBA

Board Member, Legend Biotech,
Chairman and CEO, Elpiscience Biopharmaceuticals

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Darren Ji

Darren Ji, MD, PhD and MBA

Board Member, Legend Biotech,
Chairman and CEO, Elpiscience Biopharmaceuticals

Dr. Ji has served on the board of directors at Legend Biotech since May 2020. Dr. Ji is Chairman and CEO of Elpiscience Biopharmaceuticals, a clinical stage immunotherapy company that he co-founded. He is also a Venture Partner of Lilly Asia Ventures (LAV). Prior to that Dr. Ji was Global Head and Vice President of Roche for Business Development in Asia and Emerging Markets. In this role, Dr. Ji was responsible for driving the strategy and execution of business development activities in a large territory encompassing over 100 countries. During his tenure, Dr. Ji championed and oversaw the closing of a number of key transactions between Roche and partners worldwide. He managed a global team and established a strong business network in key countries including: China, Japan, Korea, Australia/New Zealand, Russia and Brazil.

A repeat entrepreneur himself, Dr. Ji started his career at the Procter & Gamble Pharmaceuticals with increasing responsibilities in drug R&D and business development. He co-founded and managed as CEO of PharmaLegacy Laboratories in Shanghai in 2008, which became a premium CRO providing high-quality drug discovery services to a large global clientele until today. Dr. Ji has been a highly respected leader and a sought-after speaker in global business forums. He was also an avid community builder exemplified by completing one of the longest services as a board member of the BayHelix Group, a community of business leaders of Chinese heritage in the life sciences.

Dr. Ji received his Doctor of Medicine from China Medical University, China; a Doctor of Philosophy degree from University of Sheffield, UK; and a Master of Business Administration degree from the University of Chicago, USA.

Philip Yau
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Philip Yau

Board Member, Legend Biotech

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Philip Yau

Philip Yau

Board Member, Legend Biotech

Mr. Yau has served on the board of directors at Legend Biotech since May 2020. He has over 23 years of experience in accounting, finance, mergers and acquisitions, investments, corporate finance, audit, corporate governance, and risk management. Mr. Yau served as the non-executive vice chairman of AMTD Group where he advised on strategy development and corporate finance. Prior to that, Mr. Yau worked at Ernst & Young Greater China Practice as a partner and risk advisory China South market leader, serving clients in Greater China, where he advised on finance, management, risk management, and business issues.

Mr. Yau is a certified public accountant in the United States, a fellow member of the Hong Kong Institute of Certified Public Accountants in China, and a certified internal auditor with the Institute of Internal Auditors.

Mr. Yau graduated from the Lundquist College of Business of University of Oregon in the United States with a Bachelor of Arts degree in Accounting in 1997. Mr. Yau obtained his Executive Master of Business Administration degree from a joint school program by the Kellogg School of Management, Northwestern University and the Hong Kong University of Science and Technology China in 2019.

Patrick Casey
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Patrick Casey, Phd

Board Member, Legend Biotech

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Patrick Casey

Patrick Casey, Phd

Board Member, Legend Biotech

Patrick Casey, PhD, is the Senior Vice Dean of Research at the Duke-NUS Medical School and a James B. Duke Professor of Pharmacology and Cancer Biology at Duke University. Dr. Casey joined Duke University Medical Center as an Assistant Professor of Molecular Cancer Biology and Biochemistry in 1990. In 2005, Dr. Casey relocated to Singapore to spearhead the development of the Signature Research Programmes at Duke-NUS, where he currently oversees the administration and strategic planning of these programmes, and mentoring of faculty and trainees. He was also the founding Director of the Duke Center for Chemical Biology—an organization of Duke scientists dedicated to research and training in the application of fundamental chemical principles to the study of biology and the basis of disease and therapies. A recognized authority in the fields of lipid modifications of proteins and in G protein signaling, Dr. Casey has received several awards for his work, including the Established Investigator Award from the American Heart Association in 1992 and the Amgen Award from the American Society of Biochemistry and Molecular Biology in 2000. He was elected a Fellow of the American Association for the Advancement of Science in 2012. Dr. Casey serves on advisory panels for Agency for Science, Technology and Research (A*STAR), National Research Foundation (NRF) and National Medical Research Council (NMRC). Dr Casey received his PhD in Biochemistry from the Brandeis University in 1986 and did postdoctoral work at the University of Texas Southwestern Medical Center in Dallas.


Current partnerships

Collaboration with Janssen Biotech, Inc

Legend Biotech has entered into a worldwide collaboration and license agreement with Janssen Biotech, Inc., one of the Janssen Pharmaceutical Companies of Johnson & Johnson, to develop, manufacture, and commercialize ciltacabtagene autoleucel (also known as cilta-cel, LCAR-B38M, JNJ-68284528, JNJ-4528)a,b. Under the terms of the agreement, Legend and Janssen are co-developing and will co-commercialize ciltacabtagene autoleucel in select countries. Manufacturing of ciltacabtagene autoleucel for commercial distribution worldwide will be done in partnership with Janssen.

  1. The safety and efficacy of the agents and/or uses under investigation have not been established. There is no guarantee that the agents will receive health authority approval or become commercially available in any country for the uses being investigated.

  2. Ciltacabtagene autoleucel (cilta-cel) refers to both LCAR-B38M CAR-T cells and JNJ-4528. LCAR-B38M CAR-T cell identifies the investigational product being studied in China and JNJ-4528 identifies the investigational product being studied outside of China, both of which are representative of the same CAR-T cell therapy.

Collaboration with Beth Israel Deaconess Medical Center-Harvard Medical School

Legend Biotech has established a research collaboration with Beth Israel Deaconess Medical Center (BIDMC), an academic medical center affiliated with Harvard Medical School, to investigate a chimeric antigen receptor T (CAR-T) cell therapy approach for Human Immunodeficiency Virus (HIV) infections.

Dan H. Barouch, MD, PhD, Director of the Center for Virology and Vaccine Research at BIDMC, a leading researcher in virology with extensive experience in preclinical and clinical studies, serves as the principal investigator for the collaboration.

Under the terms of the agreement, Legend Biotech will engineer and provide CAR-T cell candidates against specific targets that may affect HIV viral load suppression and disease control. Dr. Barouch and team will focus on preclinical studies, and a clinical proof-of-concept study as appropriate.


Careers

At Legend Biotech, we are transforming the world of oncology and medicine, and always looking for people who can help contribute to the strength of our team and to our shared values.

We are actively hiring across multiple functions and levels to strengthen our world-class team with our goal and commitment to improving patients’ lives through transformative science and medicine.

To view and apply for one of our current open positions, visit our

LinkedIn Careers page.

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