董事介绍
注:董事持股数取自最新公司公告
| 姓名 | 性别 | 职位 | 年龄 | 薪酬 | 持股数(万股) | 截止日期 |
|---|---|---|---|---|---|---|
| Wayne P. Rothbaum | 男 | Director | 57 | 未披露 | 未持股 | 2025-08-06 |
| Iain Dukes | 男 | Chairman of the Board | 66 | 65.52万美元 | 未持股 | 2025-08-06 |
| Frederick G. Vogt | 男 | Interim Chief Executive Officer and President, General Counsel; Director | 51 | 未披露 | 未持股 | 2025-08-06 |
| Ryan D. Maynard | 男 | Director | 55 | 未披露 | 未持股 | 2025-08-06 |
| Michael Weiser | 男 | Director | 62 | 未披露 | 未持股 | 2025-08-06 |
| Athena Countouriotis | 女 | Director | 54 | 未披露 | 未持股 | 2025-08-06 |
| Wendy L. Yarno | 女 | Director | 70 | 未披露 | 未持股 | 2025-08-06 |
高管介绍
注:高管持股数取自最新公司公告
| 姓名 | 性别 | 职位 | 年龄 | 薪酬 | 持股数(万股) | 截止日期 |
|---|---|---|---|---|---|---|
| Corleen Roche | 女 | Chief Financial Officer and Principal Accounting Officer | 59 | 未披露 | 未持股 | 2025-08-06 |
| Frederick G. Vogt | 男 | Interim Chief Executive Officer and President, General Counsel; Director | 51 | 未披露 | 未持股 | 2025-08-06 |
| Daniel Gordon Kirby | 男 | Chief Commercial Officer | 53 | 未披露 | 未持股 | 2025-08-06 |
| Raj K. Puri | 男 | Chief Regulatory Officer | 69 | 未披露 | 未持股 | 2025-08-06 |
| Friedrich Graf Finckenstein | 男 | Chief Medical Officer | 58 | 未披露 | 未持股 | 2025-08-06 |
| Igor P. Bilinsky | 男 | Chief Operating Officer | 52 | 未披露 | 未持股 | 2025-08-06 |
董事简历
中英对照 |  中文 |  英文- Wayne P. Rothbaum
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Wayne P. Rothbaum, 2016年6月加入董事会。他是Quogue Capital的总裁,这是一家专注于投资和支持中小型生命科学公司的单一家族办公室私募股权基金。他的职业生涯始于战略咨询公司The Carson Group,在那里他管理其生命科学实践和精品投资银行Evolution Capital。继The Carson Group于2001年出售给Thomson Reuters之后,Rothbaum先生创立了Quogue Capital,通过该公司,他创立和/或投资了许多私人和公共生命科学公司。2012年,他共同创立并担任Acerta Pharma的执行主席,Acerta Pharma是一家私人生命科学公司,后来出售给AstraZeneca。Acerta的主要药物Calquence(acalabrutinib)于2017年被FDA批准用于套细胞淋巴瘤,并于2020年被批准用于慢性淋巴细胞白血病。2016年,他还共同创立了Kartos Therapeutics,此前安进(Amgen)的一种研究性MDM2抑制剂获得许可。最近,在2019年,他在获得默克公司(Merck KGaA)的一种新型靶向疗法许可后,与人共同创立了Telios Pharma,用于治疗选定的血癌和眼科疾病。此外,他在公司转型、重组和重组Iovance Biotherapeutics, Inc.方面担任领导角色。董事会,高级管理层和整体临床操作和战略。目前,他是Iovance Biotherapeutics, Inc.的董事会成员和最大股东。他于1990年毕业于Binghamton大学的Phi Beta Kappa,获得政治学和心理学双专业,并获得George Washington大学的国际经济学硕士学位。他被列为许多科学专利的发明人,并在许多医学期刊上发表,包括《新英格兰医学杂志》、《柳叶刀》和《临床肿瘤学杂志》。
Wayne P. Rothbaum,joined Board of Directors in June 2016. Mr. Rothbaum is president of Quogue Capital, a single-family office private equity fund focused on investing and supporting small to midcap life sciences companies. Mr. Rothbaum began his career at The Carson Group, a strategic consulting firm, where he managed its life sciences practice and boutique investment bank Evolution Capital. Following The Carson Group's sale to Thomson Reuters in 2001, Mr. Rothbaum founded Quogue Capital, through which he has founded and/or invested in numerous private and public life sciences companies. In 2012, Mr. Rothbaum co-founded and was the Executive Chairman of Acerta Pharma, a private life sciences company he later sold to AstraZeneca. Acerta's lead drug, Calquence (acalabrutinib) was approved by the FDA for mantle cell lymphoma in 2017 and chronic lymphocytic leukemia in 2020. In 2016, Mr. Rothbaum also co-founded Kartos Therapeutics following the in-license of an investigational MDM2 inhibitor from Amgen. More recently, in 2019, he co-founded Telios Pharma after licensing a novel targeted therapy from Merck KGaA to treat selected blood cancers and ophthalmology diseases. Additionally, Mr. Rothbaum has taken a leadership role in transforming the Company, restructuring and reorganizing Iovance Biotherapeutics, Inc. Board of Directors, senior management and overall clinical operations and strategy. Currently, Mr. Rothbaum is a board member and Iovance Biotherapeutics, Inc. largest shareholder. Mr. Rothbaum graduated Phi Beta Kappa from Binghamton University in 1990 with a dual major in political science and psychology and received his MA in international economics from The George Washington University. He is listed as an inventor on many scientific patents and is published in numerous medical journals, including The New England Journal of Medicine, The Lancet and the Journal of Clinical Oncology. - Wayne P. Rothbaum, 2016年6月加入董事会。他是Quogue Capital的总裁,这是一家专注于投资和支持中小型生命科学公司的单一家族办公室私募股权基金。他的职业生涯始于战略咨询公司The Carson Group,在那里他管理其生命科学实践和精品投资银行Evolution Capital。继The Carson Group于2001年出售给Thomson Reuters之后,Rothbaum先生创立了Quogue Capital,通过该公司,他创立和/或投资了许多私人和公共生命科学公司。2012年,他共同创立并担任Acerta Pharma的执行主席,Acerta Pharma是一家私人生命科学公司,后来出售给AstraZeneca。Acerta的主要药物Calquence(acalabrutinib)于2017年被FDA批准用于套细胞淋巴瘤,并于2020年被批准用于慢性淋巴细胞白血病。2016年,他还共同创立了Kartos Therapeutics,此前安进(Amgen)的一种研究性MDM2抑制剂获得许可。最近,在2019年,他在获得默克公司(Merck KGaA)的一种新型靶向疗法许可后,与人共同创立了Telios Pharma,用于治疗选定的血癌和眼科疾病。此外,他在公司转型、重组和重组Iovance Biotherapeutics, Inc.方面担任领导角色。董事会,高级管理层和整体临床操作和战略。目前,他是Iovance Biotherapeutics, Inc.的董事会成员和最大股东。他于1990年毕业于Binghamton大学的Phi Beta Kappa,获得政治学和心理学双专业,并获得George Washington大学的国际经济学硕士学位。他被列为许多科学专利的发明人,并在许多医学期刊上发表,包括《新英格兰医学杂志》、《柳叶刀》和《临床肿瘤学杂志》。
- Wayne P. Rothbaum,joined Board of Directors in June 2016. Mr. Rothbaum is president of Quogue Capital, a single-family office private equity fund focused on investing and supporting small to midcap life sciences companies. Mr. Rothbaum began his career at The Carson Group, a strategic consulting firm, where he managed its life sciences practice and boutique investment bank Evolution Capital. Following The Carson Group's sale to Thomson Reuters in 2001, Mr. Rothbaum founded Quogue Capital, through which he has founded and/or invested in numerous private and public life sciences companies. In 2012, Mr. Rothbaum co-founded and was the Executive Chairman of Acerta Pharma, a private life sciences company he later sold to AstraZeneca. Acerta's lead drug, Calquence (acalabrutinib) was approved by the FDA for mantle cell lymphoma in 2017 and chronic lymphocytic leukemia in 2020. In 2016, Mr. Rothbaum also co-founded Kartos Therapeutics following the in-license of an investigational MDM2 inhibitor from Amgen. More recently, in 2019, he co-founded Telios Pharma after licensing a novel targeted therapy from Merck KGaA to treat selected blood cancers and ophthalmology diseases. Additionally, Mr. Rothbaum has taken a leadership role in transforming the Company, restructuring and reorganizing Iovance Biotherapeutics, Inc. Board of Directors, senior management and overall clinical operations and strategy. Currently, Mr. Rothbaum is a board member and Iovance Biotherapeutics, Inc. largest shareholder. Mr. Rothbaum graduated Phi Beta Kappa from Binghamton University in 1990 with a dual major in political science and psychology and received his MA in international economics from The George Washington University. He is listed as an inventor on many scientific patents and is published in numerous medical journals, including The New England Journal of Medicine, The Lancet and the Journal of Clinical Oncology.
- Iain Dukes
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Iain Dukes于2016年8月4日加入我们的董事会,并于2016年8月16日被任命为董事长。Dukes博士目前是OrbiMed Advisors LLC的风险合伙人。他此前曾担任Merck Research Laboratories的高级副总裁兼业务开发和许可主管(直到2016年5月)。他于2013年8月加入Merck公司。加入Merck之前,Dukes从2010年8月到2013年8月担任Amgen外部研发副总裁。Dukes从2007年到2010年担任Essentialis Therapeutics(一家临床阶段生物技术公司,专注于开发治疗罕见代谢疾病的突破性药物)总裁、首席执行官和董事会成员。Dukes从2000年到2007年担任GlaxoSmithKline科学和技术许可Vice President,在此之前,从1990年到1999年,他在Glaxo Wellcome担任多个职位,包括代谢和泌尿生殖道疾病勘探开发主管和离子通道药物发现集团主管。Dukes博士拥有牛津大学(University of Oxford)法学硕士和哲学博士学位,利兹大学(University of Leeds)心血管研究理学硕士学位和巴斯大学(University of Bath)药理学理学学士学位。
Iain Dukes has served as Traws Pharma, Inc. Chief Executive Officer since October 1, 2025, prior to which he served as Traws Pharma, Inc. Interim Chief Executive Officer commencing as of April 1, 2025. Dr. Dukes is a Venture Partner at OrbiMed Advisors LLC, a global investment firm, which he joined in Augt 2016. He has also served in a consulting role as Chief Executive Officer and as Chairman of Lomond Therapeutics Holdings, Inc. ("Lomond") since November 1, 2024 (prior to which, commencing in January 2020, he served as Chairman of Lomond Therapeutics, Inc., which became a wholly owned subsidiary of Lomond through a merger on November 1, 2024), as the Executive Chairman of Angiex Inc. since February 2020, the Chief Executive Officer and Chairman of Eilean Therapeutics LLC since July 2022 and as Chairman of vario private companies forming the Loch Group of companies. In September 2017, Dr. Dukes co founded Kartos Therapeutics, Inc., and he currently serves as its President and as a member of its board of directors. Dr. Dukes also co founded Telios Pharmaceuticals, Inc., where he serves as President. From February 2019 to December 2024, Dr. Dukes served as the Chief Executive Officer of Viriom Inc. In June 2018, Dr. Dukes co founded These Pharmaceuticals, Inc., where he served as Chairman and director until its acquisition by Concentra Biosciences, LLC in April 2024. Dr. Dukes previoly served as Senior Vice President and Head of Biness Development and Licensing for Merck Research Laboratories. Prior to joining Merck, Dr. Dukes served as Vice President of External Research and Development at Amgen, Inc. He has also served as President and Chief Executive Officer, as ll as a member of the Board of Directors, of Essentialis Therapeutics, a clinical stage biotechnology company foced on the development of breakthrough medicines for the treatment of rare metabolic diseases. Previoly, Dr. Dukes served as Vice President of Scientific and Technology Licensing at GlaxoSmithKline, and he held vario positions at Glaxo llcome, including Head of Exploratory Development for Metabolic and Urogenital Diseases and Head of Ion channel drug Discovery Group. From October 2017 to July 2020, Dr. Dukes was a board member and Chairman of KaNDy Therapeutics, which was acquired by Bayer AG in September 2020. From January 2020 to June 2020, Dr. Dukes served as supervisory board member of Themis BioScience GmbH, until it was acquired by Merck & Co. Dr. Dukes is currently the chairman of the board of directors of Iovance Biotherapeutics, Inc. (Nasdaq: IOVA) and also serves on the board of directors of Ikena Oncology (Nasdaq: IKNA), NeRRe Therapeutics, ENYO Therapeutics, Feldan Therapeutics and Rathlin Therapeutics Ltd. He holds an M.A. in Jurisprudence. and D.Phil. from the University of Oxford, an M.Sc. in Cardiovascular Studies from the University of Leeds, and a B.Sc. in Pharmacology from the University of Bath. - Iain Dukes于2016年8月4日加入我们的董事会,并于2016年8月16日被任命为董事长。Dukes博士目前是OrbiMed Advisors LLC的风险合伙人。他此前曾担任Merck Research Laboratories的高级副总裁兼业务开发和许可主管(直到2016年5月)。他于2013年8月加入Merck公司。加入Merck之前,Dukes从2010年8月到2013年8月担任Amgen外部研发副总裁。Dukes从2007年到2010年担任Essentialis Therapeutics(一家临床阶段生物技术公司,专注于开发治疗罕见代谢疾病的突破性药物)总裁、首席执行官和董事会成员。Dukes从2000年到2007年担任GlaxoSmithKline科学和技术许可Vice President,在此之前,从1990年到1999年,他在Glaxo Wellcome担任多个职位,包括代谢和泌尿生殖道疾病勘探开发主管和离子通道药物发现集团主管。Dukes博士拥有牛津大学(University of Oxford)法学硕士和哲学博士学位,利兹大学(University of Leeds)心血管研究理学硕士学位和巴斯大学(University of Bath)药理学理学学士学位。
- Iain Dukes has served as Traws Pharma, Inc. Chief Executive Officer since October 1, 2025, prior to which he served as Traws Pharma, Inc. Interim Chief Executive Officer commencing as of April 1, 2025. Dr. Dukes is a Venture Partner at OrbiMed Advisors LLC, a global investment firm, which he joined in Augt 2016. He has also served in a consulting role as Chief Executive Officer and as Chairman of Lomond Therapeutics Holdings, Inc. ("Lomond") since November 1, 2024 (prior to which, commencing in January 2020, he served as Chairman of Lomond Therapeutics, Inc., which became a wholly owned subsidiary of Lomond through a merger on November 1, 2024), as the Executive Chairman of Angiex Inc. since February 2020, the Chief Executive Officer and Chairman of Eilean Therapeutics LLC since July 2022 and as Chairman of vario private companies forming the Loch Group of companies. In September 2017, Dr. Dukes co founded Kartos Therapeutics, Inc., and he currently serves as its President and as a member of its board of directors. Dr. Dukes also co founded Telios Pharmaceuticals, Inc., where he serves as President. From February 2019 to December 2024, Dr. Dukes served as the Chief Executive Officer of Viriom Inc. In June 2018, Dr. Dukes co founded These Pharmaceuticals, Inc., where he served as Chairman and director until its acquisition by Concentra Biosciences, LLC in April 2024. Dr. Dukes previoly served as Senior Vice President and Head of Biness Development and Licensing for Merck Research Laboratories. Prior to joining Merck, Dr. Dukes served as Vice President of External Research and Development at Amgen, Inc. He has also served as President and Chief Executive Officer, as ll as a member of the Board of Directors, of Essentialis Therapeutics, a clinical stage biotechnology company foced on the development of breakthrough medicines for the treatment of rare metabolic diseases. Previoly, Dr. Dukes served as Vice President of Scientific and Technology Licensing at GlaxoSmithKline, and he held vario positions at Glaxo llcome, including Head of Exploratory Development for Metabolic and Urogenital Diseases and Head of Ion channel drug Discovery Group. From October 2017 to July 2020, Dr. Dukes was a board member and Chairman of KaNDy Therapeutics, which was acquired by Bayer AG in September 2020. From January 2020 to June 2020, Dr. Dukes served as supervisory board member of Themis BioScience GmbH, until it was acquired by Merck & Co. Dr. Dukes is currently the chairman of the board of directors of Iovance Biotherapeutics, Inc. (Nasdaq: IOVA) and also serves on the board of directors of Ikena Oncology (Nasdaq: IKNA), NeRRe Therapeutics, ENYO Therapeutics, Feldan Therapeutics and Rathlin Therapeutics Ltd. He holds an M.A. in Jurisprudence. and D.Phil. from the University of Oxford, an M.Sc. in Cardiovascular Studies from the University of Leeds, and a B.Sc. in Pharmacology from the University of Bath.
- Frederick G. Vogt
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Frederick G. Vogt,于2021年6月10日成为临时首席执行官兼总裁,并于2017年7月1日成为Iovance Biotherapeutics, Inc.总法律顾问。原于2016年9月加入公司,25年医药、生物制药行业从业经验。在与公司合作的八年多时间里,Vogt博士领导了Iovance细胞治疗中心(“iCTC”)的建设、Proleukin的收购以及Amtagvi的批准和上市,以及其他重大成就。在加入Iovance之前,Vogt博士在Morgan,Lewis & Bockius LLP国际事务所从事法律业务,专注于生命科学领域的知识产权和商业法,并在专利战略、交易和诉讼事务方面代表客户。此前,他在葛兰素史克的13年里担任过许多科学、管理和法律方面的角色,责任越来越大,在那里他主要专注于肿瘤学和心血管药物开发。在GSK期间,Vogt博士为Hycamtin、Votrient、Tafinlar和Mekinist的开发和批准做出了贡献。Vogt博士拥有Ursinus学院的化学学士学位、宾夕法尼亚州立大学的化学博士学位和天普大学的法学博士学位。他撰写或合著了70多篇研究论文和书籍章节,是药物开发和生命科学领域众多专利申请的共同发明人。他获准在宾夕法尼亚州执业,并在美国专利商标局、美国宾夕法尼亚州东区地方法院和美国联邦巡回上诉法院任职。
Frederick G. Vogt,became Interim Chief Executive Officer and President on June 10, 2021, and became Iovance Biotherapeutics, Inc. General Counsel on July 1, 2017. He originally joined the Company in September 2016, and has 25 years of experience in the pharmaceutical and biopharmaceutical industries. Over more than eight years with the Company, Dr. Vogt has led construction of the Iovance Cell Therapy Center (the "iCTC"), acquisition of Proleukin, and approval and launch of Amtagvi, among other major accomplishments. Prior to joining Iovance, Dr. Vogt practiced law at the international firm of Morgan, Lewis & Bockius LLP, focusing on intellectual property and business law in the life sciences and representing clients in patent strategy, transactional, and litigation matters.Previously he served in numerous scientific, management, and legal roles of increasing responsibility over a period of 13 years at GlaxoSmithKline, where he focused primarily on oncology and cardiovascular drug development. While at GSK, Dr. Vogt made contributions to the development and approval of Hycamtin, Votrient, Tafinlar, and Mekinist. Dr. Vogt holds a B.S. in Chemistry from Ursinus College, a Ph.D. in Chemistry from the Pennsylvania State University, and a J.D. from Temple University. He has authored or co-authored more than 70 research papers and book chapters and is a co-inventor of numerous patent applications in the drug development and life sciences fields. He is admitted to practice in Pennsylvania and before the U.S. Patent and Trademark Office, the U.S. District Court for the Eastern District of Pennsylvania, and the U.S. Court of Appeals for the Federal Circuit. - Frederick G. Vogt,于2021年6月10日成为临时首席执行官兼总裁,并于2017年7月1日成为Iovance Biotherapeutics, Inc.总法律顾问。原于2016年9月加入公司,25年医药、生物制药行业从业经验。在与公司合作的八年多时间里,Vogt博士领导了Iovance细胞治疗中心(“iCTC”)的建设、Proleukin的收购以及Amtagvi的批准和上市,以及其他重大成就。在加入Iovance之前,Vogt博士在Morgan,Lewis & Bockius LLP国际事务所从事法律业务,专注于生命科学领域的知识产权和商业法,并在专利战略、交易和诉讼事务方面代表客户。此前,他在葛兰素史克的13年里担任过许多科学、管理和法律方面的角色,责任越来越大,在那里他主要专注于肿瘤学和心血管药物开发。在GSK期间,Vogt博士为Hycamtin、Votrient、Tafinlar和Mekinist的开发和批准做出了贡献。Vogt博士拥有Ursinus学院的化学学士学位、宾夕法尼亚州立大学的化学博士学位和天普大学的法学博士学位。他撰写或合著了70多篇研究论文和书籍章节,是药物开发和生命科学领域众多专利申请的共同发明人。他获准在宾夕法尼亚州执业,并在美国专利商标局、美国宾夕法尼亚州东区地方法院和美国联邦巡回上诉法院任职。
- Frederick G. Vogt,became Interim Chief Executive Officer and President on June 10, 2021, and became Iovance Biotherapeutics, Inc. General Counsel on July 1, 2017. He originally joined the Company in September 2016, and has 25 years of experience in the pharmaceutical and biopharmaceutical industries. Over more than eight years with the Company, Dr. Vogt has led construction of the Iovance Cell Therapy Center (the "iCTC"), acquisition of Proleukin, and approval and launch of Amtagvi, among other major accomplishments. Prior to joining Iovance, Dr. Vogt practiced law at the international firm of Morgan, Lewis & Bockius LLP, focusing on intellectual property and business law in the life sciences and representing clients in patent strategy, transactional, and litigation matters.Previously he served in numerous scientific, management, and legal roles of increasing responsibility over a period of 13 years at GlaxoSmithKline, where he focused primarily on oncology and cardiovascular drug development. While at GSK, Dr. Vogt made contributions to the development and approval of Hycamtin, Votrient, Tafinlar, and Mekinist. Dr. Vogt holds a B.S. in Chemistry from Ursinus College, a Ph.D. in Chemistry from the Pennsylvania State University, and a J.D. from Temple University. He has authored or co-authored more than 70 research papers and book chapters and is a co-inventor of numerous patent applications in the drug development and life sciences fields. He is admitted to practice in Pennsylvania and before the U.S. Patent and Trademark Office, the U.S. District Court for the Eastern District of Pennsylvania, and the U.S. Court of Appeals for the Federal Circuit.
- Ryan D. Maynard
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Ryan D. Maynard,2010年3月起,担任本公司的执行副总裁、首席财务官。他于2001年9月加入Rigel,担任企业财务总监;2001年10月,被任命为助理秘书。2006年6月,他成为财务副总裁、代理首席财务官;2007年1月,成为副总裁、首席财务官。加入Rigel之前,1999年11月至2001年4月,他担任Personify的企业财务总监、财务与会计总监,这是一个电子商务软件公司。1998年7月至1999年10月,他担任General Magic的财务总监;1994年7月至1998年6月,他在Siliconix担任过多个职务,最后的是高级财务经理。之前,他曾任职于Ernst & Young,期间成为注册会计师。他获得了Santa Clara University的商业会计学士学位。
Ryan D. Maynard,joined Board of Directors in February 2015. Mr. Maynard served as Chief Financial Officer of Cara Therapeutics, Inc., a publicly traded commercial-stage biopharmaceutical company, through April 2025. Previously he served as the Chief Financial Officer of LetsGetChecked, from October 2019 to early 2022. Mr. Maynard was the Chief Financial Officer of Blade Therapeutics, Inc., a privately held biotechnology company, from February 2018 to June 2019. Until December 2017, he was the Executive Vice President and Chief Financial Officer of Rigel Pharmaceuticals, Inc., a public commercial-stage drug development company. He joined Rigel in September 2001 as Corporate Controller and was appointed as an Assistant Secretary in October 2001. In June 2006 he became Rigel's Vice President of Finance and Acting Chief Financial Officer and became its Vice President and Chief Financial Officer in January 2007. Prior to joining Rigel, Mr. Maynard was Corporate Controller and Director of Finance and Accounting for Personify, Inc., an e-commerce software company, from November 1999 to April 2001. From July 1998 to October 1999, he served as Controller of General Magic, Inc. and from July 1994 to June 1998 he held various positions at Siliconix, Inc., most recently as Senior Finance Manager. He previously worked at Ernst & Young LLP. Mr. Maynard holds a B.S. in Commerce - Accounting from Santa Clara University. - Ryan D. Maynard,2010年3月起,担任本公司的执行副总裁、首席财务官。他于2001年9月加入Rigel,担任企业财务总监;2001年10月,被任命为助理秘书。2006年6月,他成为财务副总裁、代理首席财务官;2007年1月,成为副总裁、首席财务官。加入Rigel之前,1999年11月至2001年4月,他担任Personify的企业财务总监、财务与会计总监,这是一个电子商务软件公司。1998年7月至1999年10月,他担任General Magic的财务总监;1994年7月至1998年6月,他在Siliconix担任过多个职务,最后的是高级财务经理。之前,他曾任职于Ernst & Young,期间成为注册会计师。他获得了Santa Clara University的商业会计学士学位。
- Ryan D. Maynard,joined Board of Directors in February 2015. Mr. Maynard served as Chief Financial Officer of Cara Therapeutics, Inc., a publicly traded commercial-stage biopharmaceutical company, through April 2025. Previously he served as the Chief Financial Officer of LetsGetChecked, from October 2019 to early 2022. Mr. Maynard was the Chief Financial Officer of Blade Therapeutics, Inc., a privately held biotechnology company, from February 2018 to June 2019. Until December 2017, he was the Executive Vice President and Chief Financial Officer of Rigel Pharmaceuticals, Inc., a public commercial-stage drug development company. He joined Rigel in September 2001 as Corporate Controller and was appointed as an Assistant Secretary in October 2001. In June 2006 he became Rigel's Vice President of Finance and Acting Chief Financial Officer and became its Vice President and Chief Financial Officer in January 2007. Prior to joining Rigel, Mr. Maynard was Corporate Controller and Director of Finance and Accounting for Personify, Inc., an e-commerce software company, from November 1999 to April 2001. From July 1998 to October 1999, he served as Controller of General Magic, Inc. and from July 1994 to June 1998 he held various positions at Siliconix, Inc., most recently as Senior Finance Manager. He previously worked at Ernst & Young LLP. Mr. Maynard holds a B.S. in Commerce - Accounting from Santa Clara University.
- Michael Weiser
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Michael Weiser自2005年9月收购ZIOPHARM,Inc.起担任董事之一,此前自ZIOPHARM,Inc.于2003年9月成立以来担任董事。Weiser博士目前是Actin Biomed的创始人兼联席董事长,这是一家总部位于纽约的医疗保健投资公司,致力于推动新疗法的发现和开发,以满足未满足的医疗需求。此外,Weiser博士还获得了学术和专业卓越奖,并在医学和科学期刊上广泛发表。Weiser博士是美国国家医学荣誉学会、Alpha Omega Alpha、美国临床肿瘤学会、美国血液学会和视觉与眼科研究协会的成员。Weiser博士目前担任生物制药公司Emisphere Technologies,Inc.的董事会成员,以及多家私营公司的董事会成员。Weiser博士此前曾担任切尔西医疗国际、Hana Biosciences,Inc.、Manhattan Pharmaceuticals,Inc.和Vioquest Pharmaceuticals,Inc.的董事。Weiser博士在康奈尔大学医学院完成分子神经生物学博士学位,并在纽约大学医学院获得医学博士学位。他在纽约大学医学中心的妇产科进行了研究生医学培训。Weiser博士还在纽约大学医学院的生理学和神经科学系完成了博士后奖学金,并获得了佛蒙特大学的心理学学士学位。
Michael Weiser has been one of directors since September 2005 acquisition of ZIOPHARM, Inc. and previously served as a director of ZIOPHARM, Inc. since its inception in September 2003. Dr. Weiser is currently founder and co-chairman of Actin Biomed, a New York-based healthcare investment firm advancing the discovery and development of novel treatments for unmet medical needs. In addition, Dr. Weiser has received awards for both academic and professional excellence and is published extensively in both medical and scientific journals. Dr. Weiser is a member of The National Medical Honor Society, Alpha Omega Alpha, American Society of Clinical Oncology, American Society of Hematology and Association for Research in Vision and Ophthalmology. Dr. Weiser currently serves on the board of directors of Emisphere Technologies, Inc., a biopharmaceutical company, as well as on the board of directors of several privately held companies. Dr. Weiser previously served as a director of Chelsea Therapeutics International, Hana Biosciences, Inc., Manhattan Pharmaceuticals, Inc. and Vioquest Pharmaceuticals, Inc. Dr. Weiser completed his Ph.D. in Molecular Neurobiology at Cornell University Medical College and received his M.D. from New York University School of Medicine. He performed his post-graduate medical training in the Department of Obstetrics and Gynecology at New York University Medical Center. Dr. Weiser also completed a Postdoctoral Fellowship in the Department of Physiology and Neuroscience at New York University School of Medicine and received his B.A. in psychology from University of Vermont. - Michael Weiser自2005年9月收购ZIOPHARM,Inc.起担任董事之一,此前自ZIOPHARM,Inc.于2003年9月成立以来担任董事。Weiser博士目前是Actin Biomed的创始人兼联席董事长,这是一家总部位于纽约的医疗保健投资公司,致力于推动新疗法的发现和开发,以满足未满足的医疗需求。此外,Weiser博士还获得了学术和专业卓越奖,并在医学和科学期刊上广泛发表。Weiser博士是美国国家医学荣誉学会、Alpha Omega Alpha、美国临床肿瘤学会、美国血液学会和视觉与眼科研究协会的成员。Weiser博士目前担任生物制药公司Emisphere Technologies,Inc.的董事会成员,以及多家私营公司的董事会成员。Weiser博士此前曾担任切尔西医疗国际、Hana Biosciences,Inc.、Manhattan Pharmaceuticals,Inc.和Vioquest Pharmaceuticals,Inc.的董事。Weiser博士在康奈尔大学医学院完成分子神经生物学博士学位,并在纽约大学医学院获得医学博士学位。他在纽约大学医学中心的妇产科进行了研究生医学培训。Weiser博士还在纽约大学医学院的生理学和神经科学系完成了博士后奖学金,并获得了佛蒙特大学的心理学学士学位。
- Michael Weiser has been one of directors since September 2005 acquisition of ZIOPHARM, Inc. and previously served as a director of ZIOPHARM, Inc. since its inception in September 2003. Dr. Weiser is currently founder and co-chairman of Actin Biomed, a New York-based healthcare investment firm advancing the discovery and development of novel treatments for unmet medical needs. In addition, Dr. Weiser has received awards for both academic and professional excellence and is published extensively in both medical and scientific journals. Dr. Weiser is a member of The National Medical Honor Society, Alpha Omega Alpha, American Society of Clinical Oncology, American Society of Hematology and Association for Research in Vision and Ophthalmology. Dr. Weiser currently serves on the board of directors of Emisphere Technologies, Inc., a biopharmaceutical company, as well as on the board of directors of several privately held companies. Dr. Weiser previously served as a director of Chelsea Therapeutics International, Hana Biosciences, Inc., Manhattan Pharmaceuticals, Inc. and Vioquest Pharmaceuticals, Inc. Dr. Weiser completed his Ph.D. in Molecular Neurobiology at Cornell University Medical College and received his M.D. from New York University School of Medicine. He performed his post-graduate medical training in the Department of Obstetrics and Gynecology at New York University Medical Center. Dr. Weiser also completed a Postdoctoral Fellowship in the Department of Physiology and Neuroscience at New York University School of Medicine and received his B.A. in psychology from University of Vermont.
- Athena Countouriotis
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Athena Countouriotis自2018年10月起担任Turning Point医疗公司的首席执行官和董事会成员,并于2018年5月至2018年9月期间担任Turning Point医疗的首席医疗官。Countouriotis博士于2017年6月至2018年5月担任Adverum生物科技公司高级副总裁兼首席医疗官,在此之前于2015年1月至2017年5月担任奥洛兹美医疗公司高级副总裁兼首席医疗官。Countouriotis博士还从2012年2月起担任Ambit Biosciences Corporation的首席医疗官,直到2014年11月Ambit被Daiichi Sankyo公司收购。在她职业生涯的早期,Countouriotis博士曾领导辉瑞公司和百时美施贵宝公司内的多个肿瘤治疗临床开发组织。Countouriotis博士目前在Iovance Biotherapeutics,Inc.和Trovagene,Inc.的董事会任职,这两家公司都是上市的肿瘤治疗公司。Countouriotis博士获得了加州大学洛杉矶分校的学士学位和塔夫茨大学医学院的医学博士学位。她在加州大学洛杉矶分校接受了最初的儿科培训,并在Fred Hutchinson癌症研究中心接受了儿科血液学/肿瘤学项目的额外培训。
Athena Countouriotis has served as Chief Executive Officer and a member of the board of directors of Turning Point Therapeutics Inc. since October 2018 and from May 2018 to September 2018 she served as Chief Medical Officer of Turning Point Therapeutics. Dr. Countouriotis served as Senior Vice President and Chief Medical Officer for Adverum Biotechnologies, Inc. from June 2017 to May 2018 and before that served as Senior Vice President, Chief Medical Officer of Halozyme Therapeutics, Inc. from January 2015 to May 2017. Dr. Countouriotis also served as Chief Medical Officer of Ambit Biosciences Corporation from February 2012 until Ambit's acquisition by Daiichi Sankyo Company in November 2014. Earlier in her career, Dr. Countouriotis led various clinical development organizations within Pfizer Inc. and Bristol-Myers Squibb Company for oncology therapeutics. Dr. Countouriotis currently serves on the boards of directors of Iovance Biotherapeutics, Inc. and Trovagene, Inc., both public oncology therapeutics companies. Dr. Countouriotis earned a B.S. from the University of California, Los Angeles, and an M.D. from Tufts University School of Medicine. She received her initial training in pediatrics at the University of California, Los Angeles, and additional training at the Fred Hutchinson Cancer Research Center in the Pediatric Hematology/Oncology Program. - Athena Countouriotis自2018年10月起担任Turning Point医疗公司的首席执行官和董事会成员,并于2018年5月至2018年9月期间担任Turning Point医疗的首席医疗官。Countouriotis博士于2017年6月至2018年5月担任Adverum生物科技公司高级副总裁兼首席医疗官,在此之前于2015年1月至2017年5月担任奥洛兹美医疗公司高级副总裁兼首席医疗官。Countouriotis博士还从2012年2月起担任Ambit Biosciences Corporation的首席医疗官,直到2014年11月Ambit被Daiichi Sankyo公司收购。在她职业生涯的早期,Countouriotis博士曾领导辉瑞公司和百时美施贵宝公司内的多个肿瘤治疗临床开发组织。Countouriotis博士目前在Iovance Biotherapeutics,Inc.和Trovagene,Inc.的董事会任职,这两家公司都是上市的肿瘤治疗公司。Countouriotis博士获得了加州大学洛杉矶分校的学士学位和塔夫茨大学医学院的医学博士学位。她在加州大学洛杉矶分校接受了最初的儿科培训,并在Fred Hutchinson癌症研究中心接受了儿科血液学/肿瘤学项目的额外培训。
- Athena Countouriotis has served as Chief Executive Officer and a member of the board of directors of Turning Point Therapeutics Inc. since October 2018 and from May 2018 to September 2018 she served as Chief Medical Officer of Turning Point Therapeutics. Dr. Countouriotis served as Senior Vice President and Chief Medical Officer for Adverum Biotechnologies, Inc. from June 2017 to May 2018 and before that served as Senior Vice President, Chief Medical Officer of Halozyme Therapeutics, Inc. from January 2015 to May 2017. Dr. Countouriotis also served as Chief Medical Officer of Ambit Biosciences Corporation from February 2012 until Ambit's acquisition by Daiichi Sankyo Company in November 2014. Earlier in her career, Dr. Countouriotis led various clinical development organizations within Pfizer Inc. and Bristol-Myers Squibb Company for oncology therapeutics. Dr. Countouriotis currently serves on the boards of directors of Iovance Biotherapeutics, Inc. and Trovagene, Inc., both public oncology therapeutics companies. Dr. Countouriotis earned a B.S. from the University of California, Los Angeles, and an M.D. from Tufts University School of Medicine. She received her initial training in pediatrics at the University of California, Los Angeles, and additional training at the Fred Hutchinson Cancer Research Center in the Pediatric Hematology/Oncology Program.
- Wendy L. Yarno
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Wendy L. Yarno,她从2013年起担任Inovio Pharmaceuticals, Inc.董事。她目前是薪酬委员会(Compensation Committee)主席及提名与公司管理委员会(Nominating and Corporate Governance Committee)成员。她在Merck & Co., Inc.商业与人力资源职位工作了26年,位至首席营销官,于2008年退休。那时,她领导一个全球性组织,主管各方对多达20个治疗领域的医药品商业化的支持。在此之前,她担任过心血管新陈代谢美国业务总经理,负责Merck最大的治疗领域的损益以及人力资源高级副总裁。从Merck退休后,从2012年9月至2011年9月,她在生物科技研究公司HemoShear LLC担任兼职首席营销官,HemoShear LLC是人类细胞替代系统领导开发者,用以探索评估新药物成分。从2011年9月起,她一直是生命科学产业的一名独立顾问。从2002年起,她担任财富500强医疗设备公司St. Jude Medical, Inc.的董事,从2013年10月起,担任Aratana Therapeutics的董事,Aratana Therapeutics是研发宠物药物的生物制药公司。她还在许多私有保健公司担任过董事和咨询董事会成员。她从波特兰州立大学(Portland State University)获得商业管理学士学位,并从天普大学(Temple University)获得工商管理学硕士学位。
Wendy L. Yarno,retired in 2008 from Merck & Company, Inc. following a 26-year career in commercial and human resource positions of increasing seniority, most recently as Chief Marketing Officer before she retired. Ms. Yarno also spent part of her career at Johnson & Johnson, Inc. in commercial positions. Ms. Yarno currently serves on the boards of directors of the publicly traded companies Ideaya Biosciences, Inc. and Tarsus Pharmaceuticals. Within the last five years, Ms. Yarno served on the board of directors of Global Blood Therapeutics, Inc., MyoKardia, Inc., Alder Biopharmaceuticals, Inc. and Aratana Therapeutics, Inc. Ms. Yarno holds a B.S. in Business Administration from Portland State University and an M.B.A. from Temple University. - Wendy L. Yarno,她从2013年起担任Inovio Pharmaceuticals, Inc.董事。她目前是薪酬委员会(Compensation Committee)主席及提名与公司管理委员会(Nominating and Corporate Governance Committee)成员。她在Merck & Co., Inc.商业与人力资源职位工作了26年,位至首席营销官,于2008年退休。那时,她领导一个全球性组织,主管各方对多达20个治疗领域的医药品商业化的支持。在此之前,她担任过心血管新陈代谢美国业务总经理,负责Merck最大的治疗领域的损益以及人力资源高级副总裁。从Merck退休后,从2012年9月至2011年9月,她在生物科技研究公司HemoShear LLC担任兼职首席营销官,HemoShear LLC是人类细胞替代系统领导开发者,用以探索评估新药物成分。从2011年9月起,她一直是生命科学产业的一名独立顾问。从2002年起,她担任财富500强医疗设备公司St. Jude Medical, Inc.的董事,从2013年10月起,担任Aratana Therapeutics的董事,Aratana Therapeutics是研发宠物药物的生物制药公司。她还在许多私有保健公司担任过董事和咨询董事会成员。她从波特兰州立大学(Portland State University)获得商业管理学士学位,并从天普大学(Temple University)获得工商管理学硕士学位。
- Wendy L. Yarno,retired in 2008 from Merck & Company, Inc. following a 26-year career in commercial and human resource positions of increasing seniority, most recently as Chief Marketing Officer before she retired. Ms. Yarno also spent part of her career at Johnson & Johnson, Inc. in commercial positions. Ms. Yarno currently serves on the boards of directors of the publicly traded companies Ideaya Biosciences, Inc. and Tarsus Pharmaceuticals. Within the last five years, Ms. Yarno served on the board of directors of Global Blood Therapeutics, Inc., MyoKardia, Inc., Alder Biopharmaceuticals, Inc. and Aratana Therapeutics, Inc. Ms. Yarno holds a B.S. in Business Administration from Portland State University and an M.B.A. from Temple University.
高管简历
中英对照 |  中文 |  英文- Corleen Roche
Corleen Roche,自2024年1月起担任CG Oncology,Inc. 首席财务官兼秘书。此前,罗氏女士于2021年4月至2024年1月期间担任生物技术上市公司Immunome, Inc.的首席财务官。在加入Immunome之前,罗氏女士于2019年至2021年4月期间担任渤健 Inc.的美国首席财务官,并于2015年至2019年期间担任诺华旗下部门Sandoz的首席财务官美国生物制药公司。罗氏女士的职业生涯始于普华永道,曾在其他公司担任首席财务官,包括IoGenetics,Inc.和惠氏制药的全球疫苗业务部门。罗氏女士拥有维拉诺瓦大学会计学学士学位。
Corleen Roche,has served as Cg Oncology, Inc. Chief Financial Officer and Secretary since January 2024. Previously, Ms. Roche served as the Chief Financial Officer of Immunome, Inc., a publicly-traded biotechnology company, from April 2021 to January 2024. Prior to Immunome, Ms. Roche served as the Chief Financial Officer, U.S. of Biogen Inc. from 2019 until April 2021, and served as the Chief Financial Officer U.S. Biopharma for Sandoz, a division of Novartis, from 2015 to 2019. Ms. Roche began her career at PricewaterhouseCoopers and has served as Chief Financial Officer at other companies including IoGenetics, Inc. and the Global Vaccines business unit at Wyeth Pharmaceuticals. Ms. Roche holds a B.A. in Accountancy from Villanova University.- Corleen Roche,自2024年1月起担任CG Oncology,Inc. 首席财务官兼秘书。此前,罗氏女士于2021年4月至2024年1月期间担任生物技术上市公司Immunome, Inc.的首席财务官。在加入Immunome之前,罗氏女士于2019年至2021年4月期间担任渤健 Inc.的美国首席财务官,并于2015年至2019年期间担任诺华旗下部门Sandoz的首席财务官美国生物制药公司。罗氏女士的职业生涯始于普华永道,曾在其他公司担任首席财务官,包括IoGenetics,Inc.和惠氏制药的全球疫苗业务部门。罗氏女士拥有维拉诺瓦大学会计学学士学位。
- Corleen Roche,has served as Cg Oncology, Inc. Chief Financial Officer and Secretary since January 2024. Previously, Ms. Roche served as the Chief Financial Officer of Immunome, Inc., a publicly-traded biotechnology company, from April 2021 to January 2024. Prior to Immunome, Ms. Roche served as the Chief Financial Officer, U.S. of Biogen Inc. from 2019 until April 2021, and served as the Chief Financial Officer U.S. Biopharma for Sandoz, a division of Novartis, from 2015 to 2019. Ms. Roche began her career at PricewaterhouseCoopers and has served as Chief Financial Officer at other companies including IoGenetics, Inc. and the Global Vaccines business unit at Wyeth Pharmaceuticals. Ms. Roche holds a B.A. in Accountancy from Villanova University.
- Frederick G. Vogt
Frederick G. Vogt,于2021年6月10日成为临时首席执行官兼总裁,并于2017年7月1日成为Iovance Biotherapeutics, Inc.总法律顾问。原于2016年9月加入公司,25年医药、生物制药行业从业经验。在与公司合作的八年多时间里,Vogt博士领导了Iovance细胞治疗中心(“iCTC”)的建设、Proleukin的收购以及Amtagvi的批准和上市,以及其他重大成就。在加入Iovance之前,Vogt博士在Morgan,Lewis & Bockius LLP国际事务所从事法律业务,专注于生命科学领域的知识产权和商业法,并在专利战略、交易和诉讼事务方面代表客户。此前,他在葛兰素史克的13年里担任过许多科学、管理和法律方面的角色,责任越来越大,在那里他主要专注于肿瘤学和心血管药物开发。在GSK期间,Vogt博士为Hycamtin、Votrient、Tafinlar和Mekinist的开发和批准做出了贡献。Vogt博士拥有Ursinus学院的化学学士学位、宾夕法尼亚州立大学的化学博士学位和天普大学的法学博士学位。他撰写或合著了70多篇研究论文和书籍章节,是药物开发和生命科学领域众多专利申请的共同发明人。他获准在宾夕法尼亚州执业,并在美国专利商标局、美国宾夕法尼亚州东区地方法院和美国联邦巡回上诉法院任职。
Frederick G. Vogt,became Interim Chief Executive Officer and President on June 10, 2021, and became Iovance Biotherapeutics, Inc. General Counsel on July 1, 2017. He originally joined the Company in September 2016, and has 25 years of experience in the pharmaceutical and biopharmaceutical industries. Over more than eight years with the Company, Dr. Vogt has led construction of the Iovance Cell Therapy Center (the "iCTC"), acquisition of Proleukin, and approval and launch of Amtagvi, among other major accomplishments. Prior to joining Iovance, Dr. Vogt practiced law at the international firm of Morgan, Lewis & Bockius LLP, focusing on intellectual property and business law in the life sciences and representing clients in patent strategy, transactional, and litigation matters.Previously he served in numerous scientific, management, and legal roles of increasing responsibility over a period of 13 years at GlaxoSmithKline, where he focused primarily on oncology and cardiovascular drug development. While at GSK, Dr. Vogt made contributions to the development and approval of Hycamtin, Votrient, Tafinlar, and Mekinist. Dr. Vogt holds a B.S. in Chemistry from Ursinus College, a Ph.D. in Chemistry from the Pennsylvania State University, and a J.D. from Temple University. He has authored or co-authored more than 70 research papers and book chapters and is a co-inventor of numerous patent applications in the drug development and life sciences fields. He is admitted to practice in Pennsylvania and before the U.S. Patent and Trademark Office, the U.S. District Court for the Eastern District of Pennsylvania, and the U.S. Court of Appeals for the Federal Circuit.- Frederick G. Vogt,于2021年6月10日成为临时首席执行官兼总裁,并于2017年7月1日成为Iovance Biotherapeutics, Inc.总法律顾问。原于2016年9月加入公司,25年医药、生物制药行业从业经验。在与公司合作的八年多时间里,Vogt博士领导了Iovance细胞治疗中心(“iCTC”)的建设、Proleukin的收购以及Amtagvi的批准和上市,以及其他重大成就。在加入Iovance之前,Vogt博士在Morgan,Lewis & Bockius LLP国际事务所从事法律业务,专注于生命科学领域的知识产权和商业法,并在专利战略、交易和诉讼事务方面代表客户。此前,他在葛兰素史克的13年里担任过许多科学、管理和法律方面的角色,责任越来越大,在那里他主要专注于肿瘤学和心血管药物开发。在GSK期间,Vogt博士为Hycamtin、Votrient、Tafinlar和Mekinist的开发和批准做出了贡献。Vogt博士拥有Ursinus学院的化学学士学位、宾夕法尼亚州立大学的化学博士学位和天普大学的法学博士学位。他撰写或合著了70多篇研究论文和书籍章节,是药物开发和生命科学领域众多专利申请的共同发明人。他获准在宾夕法尼亚州执业,并在美国专利商标局、美国宾夕法尼亚州东区地方法院和美国联邦巡回上诉法院任职。
- Frederick G. Vogt,became Interim Chief Executive Officer and President on June 10, 2021, and became Iovance Biotherapeutics, Inc. General Counsel on July 1, 2017. He originally joined the Company in September 2016, and has 25 years of experience in the pharmaceutical and biopharmaceutical industries. Over more than eight years with the Company, Dr. Vogt has led construction of the Iovance Cell Therapy Center (the "iCTC"), acquisition of Proleukin, and approval and launch of Amtagvi, among other major accomplishments. Prior to joining Iovance, Dr. Vogt practiced law at the international firm of Morgan, Lewis & Bockius LLP, focusing on intellectual property and business law in the life sciences and representing clients in patent strategy, transactional, and litigation matters.Previously he served in numerous scientific, management, and legal roles of increasing responsibility over a period of 13 years at GlaxoSmithKline, where he focused primarily on oncology and cardiovascular drug development. While at GSK, Dr. Vogt made contributions to the development and approval of Hycamtin, Votrient, Tafinlar, and Mekinist. Dr. Vogt holds a B.S. in Chemistry from Ursinus College, a Ph.D. in Chemistry from the Pennsylvania State University, and a J.D. from Temple University. He has authored or co-authored more than 70 research papers and book chapters and is a co-inventor of numerous patent applications in the drug development and life sciences fields. He is admitted to practice in Pennsylvania and before the U.S. Patent and Trademark Office, the U.S. District Court for the Eastern District of Pennsylvania, and the U.S. Court of Appeals for the Federal Circuit.
- Daniel Gordon Kirby
Daniel Gordon 卡比海运,于2025年2月加入Iovance,担任Iovance Biotherapeutics, Inc.首席商务官,带来包括细胞疗法在内的商业运营方面的深厚经验。在加入Iovance之前,卡比海运先生作为Orca Bio的首席商务官,领导了一种新兴细胞治疗平台产品的全球商业战略和运营。2018年至2020年,他在Omeros Corporation担任首席商务官,负责监督美国和欧盟针对造血干细胞移植后并发症的narsoplimab的上市准备工作,以及其已上市产品Omidria的所有商业活动。此前,他曾在Celgene(现为百时美施贵宝)担任副总裁兼美国细胞和基因主管,领导CAR T产品的市场准入、报销和营销工作。他在收购Juno Therapeutics后加入Celgene,担任营销和市场准入副总裁。在其职业生涯的早期,卡比海运先生曾担任Medivation(现为辉瑞)的营销主管,并在安进的14年任期内担任过各种商业角色,责任越来越大。
Daniel Gordon Kirby,joined Iovance in February 2025 as Iovance Biotherapeutics, Inc. Chief Commercial Officer. Prior to joining Iovance, Mr. Kirby led global commercial strategy and operations for an emerging cell therapy platform of products as Chief Commercial Officer of Orca Bio. From 2018 to 2020, he served as Chief Commercial Officer at Omeros Corporation, overseeing U.S. and EU launch readiness for narsoplimab targeting complications post hematopoietic stem cell transplantation as well as all commercial activities for their marketed product, Omidria. Previously, he led market access, reimbursement and marketing efforts for CAR T products as Vice President and Head of US Cell and Gene at Celgene (now Bristol-Myers Squibb). He joined Celgene following the acquisition of Juno Therapeutics, where he was Vice President of Marketing and Market Access. Earlier in his career, Mr. Kirby was Head of Marketing for Medivation (now Pfizer) and held various commercial roles of increasing responsibility during a 14-year tenure at Amgen.- Daniel Gordon 卡比海运,于2025年2月加入Iovance,担任Iovance Biotherapeutics, Inc.首席商务官,带来包括细胞疗法在内的商业运营方面的深厚经验。在加入Iovance之前,卡比海运先生作为Orca Bio的首席商务官,领导了一种新兴细胞治疗平台产品的全球商业战略和运营。2018年至2020年,他在Omeros Corporation担任首席商务官,负责监督美国和欧盟针对造血干细胞移植后并发症的narsoplimab的上市准备工作,以及其已上市产品Omidria的所有商业活动。此前,他曾在Celgene(现为百时美施贵宝)担任副总裁兼美国细胞和基因主管,领导CAR T产品的市场准入、报销和营销工作。他在收购Juno Therapeutics后加入Celgene,担任营销和市场准入副总裁。在其职业生涯的早期,卡比海运先生曾担任Medivation(现为辉瑞)的营销主管,并在安进的14年任期内担任过各种商业角色,责任越来越大。
- Daniel Gordon Kirby,joined Iovance in February 2025 as Iovance Biotherapeutics, Inc. Chief Commercial Officer. Prior to joining Iovance, Mr. Kirby led global commercial strategy and operations for an emerging cell therapy platform of products as Chief Commercial Officer of Orca Bio. From 2018 to 2020, he served as Chief Commercial Officer at Omeros Corporation, overseeing U.S. and EU launch readiness for narsoplimab targeting complications post hematopoietic stem cell transplantation as well as all commercial activities for their marketed product, Omidria. Previously, he led market access, reimbursement and marketing efforts for CAR T products as Vice President and Head of US Cell and Gene at Celgene (now Bristol-Myers Squibb). He joined Celgene following the acquisition of Juno Therapeutics, where he was Vice President of Marketing and Market Access. Earlier in his career, Mr. Kirby was Head of Marketing for Medivation (now Pfizer) and held various commercial roles of increasing responsibility during a 14-year tenure at Amgen.
- Raj K. Puri
Raj K. Puri,2022年3月加入Iovance,担任监管战略和转化医学执行副总裁。Puri博士于2024年11月22日晋升为首席监管官。他在评估和监管先进疗法方面拥有数十年的经验,包括细胞和基因疗法、癌症疫苗和细胞免疫疗法。普里博士此前在美国食品和药物管理局(FDA)工作了33年,其中包括在生物制剂评估和研究中心(CBER)组织和先进疗法办公室担任细胞和基因疗法(DCGT)部门主任超过19年。他还参与并监督了FDA政策和先进疗法指导文件的制定。Puri博士还是DCGT肿瘤疫苗和生物技术部门的负责人,并监督了13名主要研究人员的研究计划。作为首席研究员,在他的整个职业生涯中,普里博士领导了癌症研究和新型免疫疗法的发现。发表研究评论文章300余篇,参与科学、政府、行业和专业学会的演讲活动220余场。普里博士的发现获得了无数专利,他的许多专利被许可用于进一步的开发。在FDA期间,Puri博士与不同的公司建立了七项合作研发协议(CRADA),以开发他在癌症治疗方面的发现。曾获得FDA优异奖、FDA CBER科学成就奖、FDA专员特别引用和SITC合作者奖等众多奖项。Puri博士在美国国家癌症研究所(NCI)外科分支机构接受培训,在那里他曾在Steven Rosenberg博士的实验室工作,研究癌症的过继免疫治疗方法。普里博士还在明尼苏达州罗切斯特的梅奥诊所接受了培训。他获得了华雷斯大学医学院生物科学研究所的医学博士学位和印度勒克瑙中央药物研究所的医学科学博士学位。
Raj K. Puri,joined Iovance in March 2022 as Executive Vice President, Regulatory Strategy and Translational Medicine. Dr. Puri was promoted to Chief Regulatory Officer on November 22, 2024. He has decades of experience with the evaluation and regulation of advanced therapies, including cell and gene therapy, cancer vaccines and cellular immunotherapy. Dr. Puri previously spent 33 years working at the US Food and Drug Administration (FDA), including more than 19 years as the Director of the Division of Cellular and Gene Therapies (DCGT) in the Office of Tissues and Advanced Therapies at the Center for Biologics Evaluation and Research (CBER). He also participated and supervised development of FDA policies and guidance documents for advanced therapies. Dr. Puri was also a Chief of the Tumor Vaccines and Biotechnology Branch within DCGT and oversaw research programs of 13 principal investigators. As a Principal Investigator and throughout his career, Dr. Puri led cancer research and discovery of novel immunotherapies. He has published more than 300 research and review articles and participated in more than 220 speaking engagements at scientific, government, industry and professional societies. Dr. Puri has been granted numerous patents on his discoveries and many of his patents are licensed for further developments. While at FDA, Dr. Puri established seven Cooperative Research and Development Agreements (CRADAs) with different companies to develop his discoveries for cancer therapy. He has received numerous awards including the FDA Award of Merit, FDA CBER's Scientific Achievement Award, FDA Commissioner's Special Citations and the SITC Collaborator Award. Dr. Puri trained at the Surgery Branch of the National Cancer Institute (NCI), where he worked in the laboratory of Dr. Steven Rosenberg on adoptive immunotherapy approaches for cancer. Dr. Puri was also trained at the Mayo Clinic in Rochester, MN. He received an M.D. from the University of Juarez Medical School Institute of Biosciences and a Ph.D. in Medical Sciences from the Central Drug Research Institute, Lucknow, India.- Raj K. Puri,2022年3月加入Iovance,担任监管战略和转化医学执行副总裁。Puri博士于2024年11月22日晋升为首席监管官。他在评估和监管先进疗法方面拥有数十年的经验,包括细胞和基因疗法、癌症疫苗和细胞免疫疗法。普里博士此前在美国食品和药物管理局(FDA)工作了33年,其中包括在生物制剂评估和研究中心(CBER)组织和先进疗法办公室担任细胞和基因疗法(DCGT)部门主任超过19年。他还参与并监督了FDA政策和先进疗法指导文件的制定。Puri博士还是DCGT肿瘤疫苗和生物技术部门的负责人,并监督了13名主要研究人员的研究计划。作为首席研究员,在他的整个职业生涯中,普里博士领导了癌症研究和新型免疫疗法的发现。发表研究评论文章300余篇,参与科学、政府、行业和专业学会的演讲活动220余场。普里博士的发现获得了无数专利,他的许多专利被许可用于进一步的开发。在FDA期间,Puri博士与不同的公司建立了七项合作研发协议(CRADA),以开发他在癌症治疗方面的发现。曾获得FDA优异奖、FDA CBER科学成就奖、FDA专员特别引用和SITC合作者奖等众多奖项。Puri博士在美国国家癌症研究所(NCI)外科分支机构接受培训,在那里他曾在Steven Rosenberg博士的实验室工作,研究癌症的过继免疫治疗方法。普里博士还在明尼苏达州罗切斯特的梅奥诊所接受了培训。他获得了华雷斯大学医学院生物科学研究所的医学博士学位和印度勒克瑙中央药物研究所的医学科学博士学位。
- Raj K. Puri,joined Iovance in March 2022 as Executive Vice President, Regulatory Strategy and Translational Medicine. Dr. Puri was promoted to Chief Regulatory Officer on November 22, 2024. He has decades of experience with the evaluation and regulation of advanced therapies, including cell and gene therapy, cancer vaccines and cellular immunotherapy. Dr. Puri previously spent 33 years working at the US Food and Drug Administration (FDA), including more than 19 years as the Director of the Division of Cellular and Gene Therapies (DCGT) in the Office of Tissues and Advanced Therapies at the Center for Biologics Evaluation and Research (CBER). He also participated and supervised development of FDA policies and guidance documents for advanced therapies. Dr. Puri was also a Chief of the Tumor Vaccines and Biotechnology Branch within DCGT and oversaw research programs of 13 principal investigators. As a Principal Investigator and throughout his career, Dr. Puri led cancer research and discovery of novel immunotherapies. He has published more than 300 research and review articles and participated in more than 220 speaking engagements at scientific, government, industry and professional societies. Dr. Puri has been granted numerous patents on his discoveries and many of his patents are licensed for further developments. While at FDA, Dr. Puri established seven Cooperative Research and Development Agreements (CRADAs) with different companies to develop his discoveries for cancer therapy. He has received numerous awards including the FDA Award of Merit, FDA CBER's Scientific Achievement Award, FDA Commissioner's Special Citations and the SITC Collaborator Award. Dr. Puri trained at the Surgery Branch of the National Cancer Institute (NCI), where he worked in the laboratory of Dr. Steven Rosenberg on adoptive immunotherapy approaches for cancer. Dr. Puri was also trained at the Mayo Clinic in Rochester, MN. He received an M.D. from the University of Juarez Medical School Institute of Biosciences and a Ph.D. in Medical Sciences from the Central Drug Research Institute, Lucknow, India.
- Friedrich Graf Finckenstein
弗里德里希·格拉夫·芬肯斯坦,2019年7月加入公司担任Iovance Biotherapeutics, Inc.首席医疗官。Graf Finckenstein博士是一位医生兼科学家,在临床医学、实验室癌症研究以及生物制药行业的药物开发方面拥有数十年的经验。在加入Iovance之前,他是瑞士巴塞尔罗氏制药研究和早期开发公司肿瘤转化医学的全球主管,在那里他领导了肿瘤发现和转化领域的所有临床开发方面,包括临床试验的设计和进行、探索性开发研究和转化医学、生物标志物和个性化医疗保健战略。在此之前,Graf Finckenstein博士曾在百时美施贵宝公司担任多个临床领导职务,在那里他研究了从早期临床开发到后期的一系列产品,包括为Opdivo的批准做出的关键贡献在肺癌中。Graf Finckenstein博士拥有德国汉堡大学的医学学位。他拥有德国医学执照、儿科委员会认证,曾在路德维希研究所、圣地亚哥分院、洛杉矶儿童医院和汉堡大学进行基础癌症研究。
Friedrich Graf Finckenstein,joined the Company as Iovance Biotherapeutics, Inc. Chief Medical Officer in July 2019. Dr. Graf Finckenstein is a physician-scientist with decades of experience in clinical medicine, laboratory cancer research, and drug development in the biopharmaceutical industry. Prior to joining Iovance he was Global Head of Oncology Translational Medicine at Roche Pharma Research and Early Development in Basel, Switzerland, where he led all clinical development aspects in the Oncology Discovery and Translational Area, including the design and conduct of clinical trials, exploratory development studies and translational medicine, biomarker and personalized healthcare strategy. Prior to that, Dr. Graf Finckenstein held multiple clinical leadership roles at Bristol-Meyers Squibb Company, where he worked on an array of products from early clinical development to late stage, including key contributions to the approval of Opdivo in lung cancer. Dr. Graf Finckenstein has a medical degree from the University of Hamburg in Germany. He holds a German medical license, a pediatric board certification, and has conducted basic cancer research at the Ludwig Institute, San Diego Branch, the Children's Hospital Los Angeles and the University of Hamburg.- 弗里德里希·格拉夫·芬肯斯坦,2019年7月加入公司担任Iovance Biotherapeutics, Inc.首席医疗官。Graf Finckenstein博士是一位医生兼科学家,在临床医学、实验室癌症研究以及生物制药行业的药物开发方面拥有数十年的经验。在加入Iovance之前,他是瑞士巴塞尔罗氏制药研究和早期开发公司肿瘤转化医学的全球主管,在那里他领导了肿瘤发现和转化领域的所有临床开发方面,包括临床试验的设计和进行、探索性开发研究和转化医学、生物标志物和个性化医疗保健战略。在此之前,Graf Finckenstein博士曾在百时美施贵宝公司担任多个临床领导职务,在那里他研究了从早期临床开发到后期的一系列产品,包括为Opdivo的批准做出的关键贡献在肺癌中。Graf Finckenstein博士拥有德国汉堡大学的医学学位。他拥有德国医学执照、儿科委员会认证,曾在路德维希研究所、圣地亚哥分院、洛杉矶儿童医院和汉堡大学进行基础癌症研究。
- Friedrich Graf Finckenstein,joined the Company as Iovance Biotherapeutics, Inc. Chief Medical Officer in July 2019. Dr. Graf Finckenstein is a physician-scientist with decades of experience in clinical medicine, laboratory cancer research, and drug development in the biopharmaceutical industry. Prior to joining Iovance he was Global Head of Oncology Translational Medicine at Roche Pharma Research and Early Development in Basel, Switzerland, where he led all clinical development aspects in the Oncology Discovery and Translational Area, including the design and conduct of clinical trials, exploratory development studies and translational medicine, biomarker and personalized healthcare strategy. Prior to that, Dr. Graf Finckenstein held multiple clinical leadership roles at Bristol-Meyers Squibb Company, where he worked on an array of products from early clinical development to late stage, including key contributions to the approval of Opdivo in lung cancer. Dr. Graf Finckenstein has a medical degree from the University of Hamburg in Germany. He holds a German medical license, a pediatric board certification, and has conducted basic cancer research at the Ludwig Institute, San Diego Branch, the Children's Hospital Los Angeles and the University of Hamburg.
- Igor P. Bilinsky
Igor P. Bilinsky,自2017年1月30日起担任高级副总裁、首席运营官。Bilinsky博士此前于2016年2月至2017年1月担任Ignyta公司高级副总裁、研究运营和免疫肿瘤学总经理,在此之前自2015年9月起担任Ignyta免疫肿瘤学总经理和特别运营高级副总裁。在加入Ignyta之前,Bilinsky博士是Vical Incorporated企业发展高级副总裁,自2010年起担任该职位。Bilinsky博士在2007年加入Halozyme担任企业发展和特殊运营执行董事后,曾于2008年至2010年在奥洛兹美医疗担任业务发展和特殊运营副总裁。2005年至2007年,比林斯基博士担任Androclus Therapeutics的首席执行官,Androclus Therapeutics是一家私营生物技术公司,为自身免疫和炎症性疾病开发新型疗法。他于2004年加入Androclus,担任首席运营官。从1999年到2004年,Bilinsky博士担任管理顾问、项目负责人以及最终在波士顿咨询公司的医疗保健实践中担任负责人等职责越来越重的职位,在那里他就业务战略、运营业绩和并购为生物技术、制药和生命科学行业的公司提供建议。在加入波士顿咨询集团之前,比林斯基博士曾在Symyx Technologies和麻省理工学院“麻省理工学院”林肯实验室担任研究职务。比林斯基博士在莫斯科物理技术学院获得物理学学士学位,在麻省理工学院获得物理学博士学位。
Igor P. Bilinsky has served as Senior Vice President, Chief Operating Officer, since January 30 2017. Dr. Bilinsky previously served as Senior Vice President, Research Operations and General Manager, Immuno-Oncology of Ignyta, Inc. from February 2016 to January 2017 and before that served as Ignyta's General Manager, Immuno-Oncology and Senior Vice President, Special Operations since September 2015. Prior to joining Ignyta, Dr. Bilinsky was Senior Vice President, Corporate Development at Vical Incorporated, a position he held since 2010. Dr. Bilinsky was previously Vice President, Business Development and Special Operations at Halozyme Therapeutics from 2008 to 2010 after joining Halozyme in 2007 as Executive Director, Corporate Development and Special Operations. From 2005 to 2007 Dr. Bilinsky was Chief Executive Officer of Androclus Therapeutics, a privately-held biotechnology company developing novel therapeutics for autoimmune and inflammatory diseases. He joined Androclus in 2004 as Chief Operating Officer. From 1999 to 2004 Dr. Bilinsky served in positions of increasing responsibility as a management consultant, project leader and ultimately as principal in the healthcare practice of the Boston Consulting Group, where he advised companies in the biotechnology, pharmaceutical and life science industries on business strategy, operational performance and mergers and acquisitions. Prior to joining the Boston Consulting Group, Dr. Bilinsky worked in research positions at Symyx Technologies and the Massachusetts Institute of Technology "MIT" Lincoln Laboratory. Dr. Bilinsky received his B.S. degree in physics from the Moscow Institute of Physics and Technology and his Ph.D. degree in physics from MIT.- Igor P. Bilinsky,自2017年1月30日起担任高级副总裁、首席运营官。Bilinsky博士此前于2016年2月至2017年1月担任Ignyta公司高级副总裁、研究运营和免疫肿瘤学总经理,在此之前自2015年9月起担任Ignyta免疫肿瘤学总经理和特别运营高级副总裁。在加入Ignyta之前,Bilinsky博士是Vical Incorporated企业发展高级副总裁,自2010年起担任该职位。Bilinsky博士在2007年加入Halozyme担任企业发展和特殊运营执行董事后,曾于2008年至2010年在奥洛兹美医疗担任业务发展和特殊运营副总裁。2005年至2007年,比林斯基博士担任Androclus Therapeutics的首席执行官,Androclus Therapeutics是一家私营生物技术公司,为自身免疫和炎症性疾病开发新型疗法。他于2004年加入Androclus,担任首席运营官。从1999年到2004年,Bilinsky博士担任管理顾问、项目负责人以及最终在波士顿咨询公司的医疗保健实践中担任负责人等职责越来越重的职位,在那里他就业务战略、运营业绩和并购为生物技术、制药和生命科学行业的公司提供建议。在加入波士顿咨询集团之前,比林斯基博士曾在Symyx Technologies和麻省理工学院“麻省理工学院”林肯实验室担任研究职务。比林斯基博士在莫斯科物理技术学院获得物理学学士学位,在麻省理工学院获得物理学博士学位。
- Igor P. Bilinsky has served as Senior Vice President, Chief Operating Officer, since January 30 2017. Dr. Bilinsky previously served as Senior Vice President, Research Operations and General Manager, Immuno-Oncology of Ignyta, Inc. from February 2016 to January 2017 and before that served as Ignyta's General Manager, Immuno-Oncology and Senior Vice President, Special Operations since September 2015. Prior to joining Ignyta, Dr. Bilinsky was Senior Vice President, Corporate Development at Vical Incorporated, a position he held since 2010. Dr. Bilinsky was previously Vice President, Business Development and Special Operations at Halozyme Therapeutics from 2008 to 2010 after joining Halozyme in 2007 as Executive Director, Corporate Development and Special Operations. From 2005 to 2007 Dr. Bilinsky was Chief Executive Officer of Androclus Therapeutics, a privately-held biotechnology company developing novel therapeutics for autoimmune and inflammatory diseases. He joined Androclus in 2004 as Chief Operating Officer. From 1999 to 2004 Dr. Bilinsky served in positions of increasing responsibility as a management consultant, project leader and ultimately as principal in the healthcare practice of the Boston Consulting Group, where he advised companies in the biotechnology, pharmaceutical and life science industries on business strategy, operational performance and mergers and acquisitions. Prior to joining the Boston Consulting Group, Dr. Bilinsky worked in research positions at Symyx Technologies and the Massachusetts Institute of Technology "MIT" Lincoln Laboratory. Dr. Bilinsky received his B.S. degree in physics from the Moscow Institute of Physics and Technology and his Ph.D. degree in physics from MIT.