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
Antoine Papiernik Director 54 7.80万 未持股 2020-03-31
Dinko Valerio Chairman and Director 64 8.80万 未持股 2020-03-31
Bart Filius Director 50 未披露 未持股 2020-03-31
Theresa Heggie Director 60 未披露 未持股 2020-03-31
James Shannon Director 64 5.60万 未持股 2020-03-31
Alison Lawton Director 59 10.50万 未持股 2020-03-31

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
Daniel de Boer Chief Executive Officer 37 82.70万 未持股 2020-03-31
Gerard Platenburg Chief Innovation Officer 56 1.20万 未持股 2020-03-31
David Rodman Executive Vice President of Research & Development 65 未披露 未持股 2020-03-31
Smital Shah Chief Business & Financial Officer 44 未披露 未持股 2020-03-31

董事简历

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Antoine Papiernik

Antoine Papiernik,2014年1月起,他担任我公司监事会成员。他是Sofinnova Partners的管理合伙人,于1997年加入该公司。他曾担任许多上市公司的最初投资人和活跃的董事会成员,包括Actelion, Addex, Auris Medical, Orexo, NovusPharma(被CTI, Movetis收购,又被Shire收购), Mainstay, Pixium和 Stentys, 上述公司分别在苏黎世证交所(Zurich Stock Exchange)、纳斯达克全球市场(NASDAQ Global Market)、斯德哥尔摩证交所(Stockholm Stock Exchange)、Milan Nuovo Mercato、比利时证交所(Belgium Stock Exchange)、都柏林证交所(Dublin Stock Exchange)和泛欧证交所(EuroNext Paris)上市,还包括Cotherix (在纳斯达克首次公开募股,后被Actelion收购), CoreValve (被Medtronic收购), Fovea (被 Sanofi Aventis收购)和Ethical Oncology Science (EOS, 被Clovis Oncology收购)。 他还投资并担任私人公司MD Start, ReCor, Shockwave Medical和Reflexion Medical的董事会成员。他在宾夕法尼亚大学沃顿商学院(Wharton School of Business, University of Pennsylvania)获得工商管理硕士学位。


Antoine Papiernik has served on our supervisory board since January 2014. Mr. Papiernik is managing partner at Sofinnova Partners, which he joined in 1997 and was appointed chairman in 2017. Mr. Papiernik has been an initial investor and active board member in public companies like Actelion, Addex, Auris Medical, Shockwave Medical Inc., Orexo, NovusPharma then sold to CTI, Movetis (then sold to Shire), Mainstay Medical, Pixium Vision and Stentys, which went public respectively on the Zurich Stock Exchange, the NASDAQ Global Market, the Stockholm Stock Exchange, the Milan Nuovo Mercato, the Belgium Stock Exchange, the Dublin Stock Exchange and EuroNext Paris, in Cotherix (initially NASDAQ listed, then sold to Actelion), Core Valve (sold to Medtronic), Fovea (sold to Sanofi Aventis) Ethical Oncology Science (EOS, sold to ClovisOncology) and Recor Medical (sold to Otsuka). Mr. Papiernik is also a board member of private companies MedDay Pharmaceuticals, MD Start II, Reflexion Medical, Tissium (previously named Gecko Biomedical), SafeHeal, Highlife, Rgenix and Ablacare. Mr. Papiernik has an MBA degree from the Wharton School of Business, University of Pennsylvania.
Antoine Papiernik,2014年1月起,他担任我公司监事会成员。他是Sofinnova Partners的管理合伙人,于1997年加入该公司。他曾担任许多上市公司的最初投资人和活跃的董事会成员,包括Actelion, Addex, Auris Medical, Orexo, NovusPharma(被CTI, Movetis收购,又被Shire收购), Mainstay, Pixium和 Stentys, 上述公司分别在苏黎世证交所(Zurich Stock Exchange)、纳斯达克全球市场(NASDAQ Global Market)、斯德哥尔摩证交所(Stockholm Stock Exchange)、Milan Nuovo Mercato、比利时证交所(Belgium Stock Exchange)、都柏林证交所(Dublin Stock Exchange)和泛欧证交所(EuroNext Paris)上市,还包括Cotherix (在纳斯达克首次公开募股,后被Actelion收购), CoreValve (被Medtronic收购), Fovea (被 Sanofi Aventis收购)和Ethical Oncology Science (EOS, 被Clovis Oncology收购)。 他还投资并担任私人公司MD Start, ReCor, Shockwave Medical和Reflexion Medical的董事会成员。他在宾夕法尼亚大学沃顿商学院(Wharton School of Business, University of Pennsylvania)获得工商管理硕士学位。
Antoine Papiernik has served on our supervisory board since January 2014. Mr. Papiernik is managing partner at Sofinnova Partners, which he joined in 1997 and was appointed chairman in 2017. Mr. Papiernik has been an initial investor and active board member in public companies like Actelion, Addex, Auris Medical, Shockwave Medical Inc., Orexo, NovusPharma then sold to CTI, Movetis (then sold to Shire), Mainstay Medical, Pixium Vision and Stentys, which went public respectively on the Zurich Stock Exchange, the NASDAQ Global Market, the Stockholm Stock Exchange, the Milan Nuovo Mercato, the Belgium Stock Exchange, the Dublin Stock Exchange and EuroNext Paris, in Cotherix (initially NASDAQ listed, then sold to Actelion), Core Valve (sold to Medtronic), Fovea (sold to Sanofi Aventis) Ethical Oncology Science (EOS, sold to ClovisOncology) and Recor Medical (sold to Otsuka). Mr. Papiernik is also a board member of private companies MedDay Pharmaceuticals, MD Start II, Reflexion Medical, Tissium (previously named Gecko Biomedical), SafeHeal, Highlife, Rgenix and Ablacare. Mr. Papiernik has an MBA degree from the Wharton School of Business, University of Pennsylvania.
Dinko Valerio

Dinko Valerio,他是我公司创始人之一,目前是监事会主席。2014年1月起,他担任我公司监事会成员。他是一名科学家和有丰富经验的生物技术企业家,在上市和私人公司均有担任首席执行官和董事会成员经验。他是荷兰生物技术公司Crucell N.V。的创始人和前首席执行官、生命科学风险投资公司Aescap Venture的创始人和普通合伙人。1999年,他成为Galapagos Genomics N.V。的创始人之一, 该公司从Crucell N.V。剥离,开发药物的新颖作用方式。他是莱顿大学(University of Leiden)的造血系统基因治疗领域教授。1982年,他在阿姆斯特丹大学(University of Amsterdam)获得生物学硕士学位,1986年,在莱顿大学(University of Leiden)以优异成绩完成分子基因学博士学位。1985年,他担任旧金山Genentech Inc.的客座科学专家;1986至1987年,成为圣地亚哥Salk Institute的博士后成员。他是100多篇同行评议学术期刊的作者以及11个专利发明者。


Dinko Valerio is one of our founders and currently serves as the chairman of our Supervisory Board. Mr. Valerio has served on our supervisory board since January 2014. Mr. Valerio is a scientist and an experienced biotech entrepreneur with experience in both public and private companies as CEO and board member. Mr. Valerio is founder and former CEO of Crucell N.V., a Dutch biotech company, and founder and former general partner of Aescap Venture, a life sciences venture capital firm. In 1999 Mr. Valerio was one of the founders of Galapagos Genomics N.V., a spinout from Crucell N.V. which develops novel mode of action medicines. In 2017 Mr. Valerio became a board member of Amylon Therapeutics B.V., an 80 owned affiliate of ProQR Therapeutics N.V. Adding to his corporate experience, Mr. Valerio was appointed professor in the field of gene therapy of the hematopoietic system at the University of Leiden in 1992. He received his Master of Science degree in Biology from the University of Amsterdam in 1982 and completed his Ph.D. in Molecular Genetics with Honors at the University of Leiden in 1986. Mr. Valerio also was a visiting scientific specialist at Genentech Inc., San Francisco in 1985 and a postdoctoral fellow at the Salk Institute, San Diego from 1986 to 1987. He is an author on more than 100 articles in peer-reviewed journals and an inventor on 11 patent-families.
Dinko Valerio,他是我公司创始人之一,目前是监事会主席。2014年1月起,他担任我公司监事会成员。他是一名科学家和有丰富经验的生物技术企业家,在上市和私人公司均有担任首席执行官和董事会成员经验。他是荷兰生物技术公司Crucell N.V。的创始人和前首席执行官、生命科学风险投资公司Aescap Venture的创始人和普通合伙人。1999年,他成为Galapagos Genomics N.V。的创始人之一, 该公司从Crucell N.V。剥离,开发药物的新颖作用方式。他是莱顿大学(University of Leiden)的造血系统基因治疗领域教授。1982年,他在阿姆斯特丹大学(University of Amsterdam)获得生物学硕士学位,1986年,在莱顿大学(University of Leiden)以优异成绩完成分子基因学博士学位。1985年,他担任旧金山Genentech Inc.的客座科学专家;1986至1987年,成为圣地亚哥Salk Institute的博士后成员。他是100多篇同行评议学术期刊的作者以及11个专利发明者。
Dinko Valerio is one of our founders and currently serves as the chairman of our Supervisory Board. Mr. Valerio has served on our supervisory board since January 2014. Mr. Valerio is a scientist and an experienced biotech entrepreneur with experience in both public and private companies as CEO and board member. Mr. Valerio is founder and former CEO of Crucell N.V., a Dutch biotech company, and founder and former general partner of Aescap Venture, a life sciences venture capital firm. In 1999 Mr. Valerio was one of the founders of Galapagos Genomics N.V., a spinout from Crucell N.V. which develops novel mode of action medicines. In 2017 Mr. Valerio became a board member of Amylon Therapeutics B.V., an 80 owned affiliate of ProQR Therapeutics N.V. Adding to his corporate experience, Mr. Valerio was appointed professor in the field of gene therapy of the hematopoietic system at the University of Leiden in 1992. He received his Master of Science degree in Biology from the University of Amsterdam in 1982 and completed his Ph.D. in Molecular Genetics with Honors at the University of Leiden in 1986. Mr. Valerio also was a visiting scientific specialist at Genentech Inc., San Francisco in 1985 and a postdoctoral fellow at the Salk Institute, San Diego from 1986 to 1987. He is an author on more than 100 articles in peer-reviewed journals and an inventor on 11 patent-families.
Bart Filius

Bart Filius,工商管理硕士,2014年12月以来,他担任我们首席财务官。在此之前,他曾在Sanofi S.A.任职超过13年,在过去三年,他担任其首席财务官。在Sanofi早期,他是 Sanofi荷兰国家经理和首席财务官。在此之前,他是兼并和收购副总裁。在此期间,他领导和完成各种特许经营权的剥离。加入Sanofi之前,他是一个战略顾问。他获得INSEAD的工商管理硕士学位和Nyenrode Business University的商业学士学位。


Bart Filius is Chief Operating Officer COO and Chief Financial Officer (CFO) at Galapagos NV. He joined Galapagos in 2014 as CFO and added the role of COO in 2017. Prior to joining Galapagos, Mr. Filius held a variety of executive positions at Sanofi, where he was Vice President, CFO Europe, Country manager for The Netherlands and Vice President for Mergers & Acquisitions. Prior to joining Sanofi, Mr. Filius was a strategy consultant at Arthur D. Little. Mr. Filius has an MBA degree from INSEAD and a bachelor's degree in business from Nyenrode University.
Bart Filius,工商管理硕士,2014年12月以来,他担任我们首席财务官。在此之前,他曾在Sanofi S.A.任职超过13年,在过去三年,他担任其首席财务官。在Sanofi早期,他是 Sanofi荷兰国家经理和首席财务官。在此之前,他是兼并和收购副总裁。在此期间,他领导和完成各种特许经营权的剥离。加入Sanofi之前,他是一个战略顾问。他获得INSEAD的工商管理硕士学位和Nyenrode Business University的商业学士学位。
Bart Filius is Chief Operating Officer COO and Chief Financial Officer (CFO) at Galapagos NV. He joined Galapagos in 2014 as CFO and added the role of COO in 2017. Prior to joining Galapagos, Mr. Filius held a variety of executive positions at Sanofi, where he was Vice President, CFO Europe, Country manager for The Netherlands and Vice President for Mergers & Acquisitions. Prior to joining Sanofi, Mr. Filius was a strategy consultant at Arthur D. Little. Mr. Filius has an MBA degree from INSEAD and a bachelor's degree in business from Nyenrode University.
Theresa Heggie

Theresa Heggie自2020年6月1日起担任公司首席执行官和董事会成员。此前,她曾于2017年5月至2020年5月担任Alnylam Pharmaceuticals墓地高级副总裁,负责人。在Alnylam之前,Heggie女士曾在Bupa Group任职至2016年,并在Shire plc任职,包括罕见病业务全球商业主管和Jerini AG于2008年被Shire收购后的首席执行官。加入Shire公司之前,她曾担任Baxter梦百合公司和Janssen Pharmaceuticals公司的多种职务。她还担任Shire&8217;s Rare Disease Business的商业运营全球主管。她也任职于Biocryst Pharmaceuticals公司和ProQR Therapeutics公司的董事会。Heggie女士在康奈尔大学(Cornell University)获得学士学位。


Theresa Heggie has served as our Chief Executive Officer and a member of our board of directors since June 1 2020. Previously, she served as Senior Vice President, Head of CEMEA at Alnylam Pharmaceuticals from May 2017 to May 2020. Before Alnylam, Ms. Heggie had roles at Bupa Group until 2016 and at Shire plc, including Global Head of Commercial for its rare disease business and CEO of Jerini AG after its acquisition by Shire in 2008. Prior to joining Shire, she held a variety of positions at Baxter Healthcare and Janssen Pharmaceuticals. She also served as Global Head of Commercial Operations of Shire’s rare disease business. She also serves on the boards of directors of BioCryst Pharmaceuticals and ProQR Therapeutics. Ms. Heggie received a B.S. from Cornell University.
Theresa Heggie自2020年6月1日起担任公司首席执行官和董事会成员。此前,她曾于2017年5月至2020年5月担任Alnylam Pharmaceuticals墓地高级副总裁,负责人。在Alnylam之前,Heggie女士曾在Bupa Group任职至2016年,并在Shire plc任职,包括罕见病业务全球商业主管和Jerini AG于2008年被Shire收购后的首席执行官。加入Shire公司之前,她曾担任Baxter梦百合公司和Janssen Pharmaceuticals公司的多种职务。她还担任Shire&8217;s Rare Disease Business的商业运营全球主管。她也任职于Biocryst Pharmaceuticals公司和ProQR Therapeutics公司的董事会。Heggie女士在康奈尔大学(Cornell University)获得学士学位。
Theresa Heggie has served as our Chief Executive Officer and a member of our board of directors since June 1 2020. Previously, she served as Senior Vice President, Head of CEMEA at Alnylam Pharmaceuticals from May 2017 to May 2020. Before Alnylam, Ms. Heggie had roles at Bupa Group until 2016 and at Shire plc, including Global Head of Commercial for its rare disease business and CEO of Jerini AG after its acquisition by Shire in 2008. Prior to joining Shire, she held a variety of positions at Baxter Healthcare and Janssen Pharmaceuticals. She also served as Global Head of Commercial Operations of Shire’s rare disease business. She also serves on the boards of directors of BioCryst Pharmaceuticals and ProQR Therapeutics. Ms. Heggie received a B.S. from Cornell University.
James Shannon

James Shannon目前担任Mannkind Corporation(一家专注于糖尿病治疗的公共生物制药公司)的董事会主席,并担任ProQR Therapeutics NV(一家公共生物技术公司)的董事会主席。从2012年5月到2015年3月,他曾担任GlaxoSmithKline GSK公司(公共生物制药公司)的首席医疗官,在那里他曾负责患者安全、一般医疗治理、医疗道德和诚信事务,医疗信息以及与正在开发或市场上的任何GSK药物有关的涉及人体受试者的调查。在此之前,Shannon博士在Novartis(一家上市制药公司)工作了十多年。在公司的最后一个职位上,作为制药开发的全球主管,他负责Novartis&8217;的所有开发活动,从临床前到4期,并监督大约40亿美元的年度开发预算。Shannon博士在北爱尔兰贝尔法斯特皇后大学(Queen&8217;s University)获得科学和医学学位。他也担任Kyowa Kirin(NA)(私人生物制药公司和Kyowa Kirin的子公司)的董事会主席,以及Immodulon Therapeutics Limited(私人生物制药公司)、Leyden Labs(私人生物制药公司)和MyTomorrows的董事会成员,一个基于健康的私人平台,与药物开发商合作,为已用尽所有其他选择的患者提供早期治疗。


James Shannon,currently serves as chairman of the board of directors of MannKind Corporation, a public biopharma company focused on treatments for diabetes, and on the board of directors of ProQR Therapeutics NV, a public biotechnology company. From May 2012 to March 2015, Dr. Shannon served as the chief medical officer of GlaxoSmithKline (GSK), a public biopharma company, where he was responsible for matters of patient safety, general medical governance, medical ethics and integrity, medical information as well as investigations involving human subjects relating to any GSK medicine in development or on the market. Prior to that, Dr. Shannon spent more than a decade with Novartis, a public pharmaceutical company. In his last role with the company, as global head of pharma development, he was responsible for all of Novartis's development activities, from pre-clinical through Phase 4, and oversaw an annual development budget of approximately $4 billion. Dr. Shannon received his science and medical degrees from Queen's University in Belfast, Northern Ireland. He also serves as chairman of the board of directors of Kyowa Kirin (NA), a private biopharma company and subsidiary of Kyowa Kirin, and on the boards of directors of Leyden Labs, a private biopharma company, and MyTomorrows, a private health-based platform that collaborates with drug developers to provide early access to treatments for patients who have exhausted all other options.
James Shannon目前担任Mannkind Corporation(一家专注于糖尿病治疗的公共生物制药公司)的董事会主席,并担任ProQR Therapeutics NV(一家公共生物技术公司)的董事会主席。从2012年5月到2015年3月,他曾担任GlaxoSmithKline GSK公司(公共生物制药公司)的首席医疗官,在那里他曾负责患者安全、一般医疗治理、医疗道德和诚信事务,医疗信息以及与正在开发或市场上的任何GSK药物有关的涉及人体受试者的调查。在此之前,Shannon博士在Novartis(一家上市制药公司)工作了十多年。在公司的最后一个职位上,作为制药开发的全球主管,他负责Novartis&8217;的所有开发活动,从临床前到4期,并监督大约40亿美元的年度开发预算。Shannon博士在北爱尔兰贝尔法斯特皇后大学(Queen&8217;s University)获得科学和医学学位。他也担任Kyowa Kirin(NA)(私人生物制药公司和Kyowa Kirin的子公司)的董事会主席,以及Immodulon Therapeutics Limited(私人生物制药公司)、Leyden Labs(私人生物制药公司)和MyTomorrows的董事会成员,一个基于健康的私人平台,与药物开发商合作,为已用尽所有其他选择的患者提供早期治疗。
James Shannon,currently serves as chairman of the board of directors of MannKind Corporation, a public biopharma company focused on treatments for diabetes, and on the board of directors of ProQR Therapeutics NV, a public biotechnology company. From May 2012 to March 2015, Dr. Shannon served as the chief medical officer of GlaxoSmithKline (GSK), a public biopharma company, where he was responsible for matters of patient safety, general medical governance, medical ethics and integrity, medical information as well as investigations involving human subjects relating to any GSK medicine in development or on the market. Prior to that, Dr. Shannon spent more than a decade with Novartis, a public pharmaceutical company. In his last role with the company, as global head of pharma development, he was responsible for all of Novartis's development activities, from pre-clinical through Phase 4, and oversaw an annual development budget of approximately $4 billion. Dr. Shannon received his science and medical degrees from Queen's University in Belfast, Northern Ireland. He also serves as chairman of the board of directors of Kyowa Kirin (NA), a private biopharma company and subsidiary of Kyowa Kirin, and on the boards of directors of Leyden Labs, a private biopharma company, and MyTomorrows, a private health-based platform that collaborates with drug developers to provide early access to treatments for patients who have exhausted all other options.
Alison Lawton

Alison Lawton, 她是二类董事,并担任我们的董事(2012年11月以来)。直到2014年1月,她曾担任OvaScience公司(公开交易的生命科学公司)的首席营运官。从1991年到2013年,她曾担任Genzyme Corporation和Sanofi-Aventis公司的多种执行,并不断被提拔。此后,该公司于2011年收购Genzyme公司(均为全球生物制药公司)。她曾担任Genzyme Biosurgery公司的主管,在那里她负责Genzyme公司的全球骨科、外科和细胞疗法和再生医学业务。此前,她曾负责Genzyme公司的全球市场准入,其中包括法规事务、全球健康结果和战略定价、全球公共政策、全球产品安全与风险管理。加入Genzyme公司之前,她曾任职 Parke-Davis公司(一个制药公司,位于英国)7年。她任职于Cubist Pharmaceuticals公司(公开上市的生物制药公司)的董事会。


Alison Lawton is a Class II director who has served as a member of our Board of Directors since November 2012. Ms. Lawton has been the Chief Executive Officer, President and Director of Kaleido Biosciences, Inc. Kaleido since 2018. She previously served as President and Chief Operating Officer of Kaleido, beginning in December 2017. Ms. Lawton was Chief Operating Officer at Aura Biosciences, Inc. from 2015 to 2017. Ms. Lawton also served as Chief Operating Officer at OvaScience Inc., a life sciences company, from January 2013 to January 2014. In addition, from 2014 to 2017 Ms. Lawton served as a biotech consultant for various companies, including as Chief Operating Officer consultant at X4 Pharmaceuticals. Ms. Lawton worked at various positions of increasing responsibility at Genzyme Corporation (Genzyme) and subsequently at Sanofi-Aventis, following its 2011 acquisition of Genzyme, each a global biopharmaceutical company. Ms. Lawton served as head of Genzyme Biosurgery, where she was responsible for Genzyme’s global orthopedics, surgical and cell therapy and regenerative medicine businesses. Prior to that, Ms. Lawton oversaw Global Market Access at Genzyme, which included Regulatory Affairs, Global Health Outcomes and Strategic Pricing, Global Public Policy and Global Product Safety & Risk Management. Before joining Genzyme, Ms. Lawton worked for seven years in the United Kingdom at Parke-Davis, a pharmaceutical company. Ms. Lawton serves on the board of directors of ProQR Therapeutics, a public biopharmaceutical company. She also has served on the boards of directors of CoLucid Pharmaceuticals, Inc. until its acquisition by Eli Lilly & Co. and of Cubist Pharmaceuticals until its acquisition by Merck & Co., Inc. She is past President and Chair of the Board of Regulatory Affairs Professional Society and past FDA Advisory Committee member for the Cell and Gene Therapy Committee. She earned her B.Sc. in Pharmacology, with honors, from King’s College London.
Alison Lawton, 她是二类董事,并担任我们的董事(2012年11月以来)。直到2014年1月,她曾担任OvaScience公司(公开交易的生命科学公司)的首席营运官。从1991年到2013年,她曾担任Genzyme Corporation和Sanofi-Aventis公司的多种执行,并不断被提拔。此后,该公司于2011年收购Genzyme公司(均为全球生物制药公司)。她曾担任Genzyme Biosurgery公司的主管,在那里她负责Genzyme公司的全球骨科、外科和细胞疗法和再生医学业务。此前,她曾负责Genzyme公司的全球市场准入,其中包括法规事务、全球健康结果和战略定价、全球公共政策、全球产品安全与风险管理。加入Genzyme公司之前,她曾任职 Parke-Davis公司(一个制药公司,位于英国)7年。她任职于Cubist Pharmaceuticals公司(公开上市的生物制药公司)的董事会。
Alison Lawton is a Class II director who has served as a member of our Board of Directors since November 2012. Ms. Lawton has been the Chief Executive Officer, President and Director of Kaleido Biosciences, Inc. Kaleido since 2018. She previously served as President and Chief Operating Officer of Kaleido, beginning in December 2017. Ms. Lawton was Chief Operating Officer at Aura Biosciences, Inc. from 2015 to 2017. Ms. Lawton also served as Chief Operating Officer at OvaScience Inc., a life sciences company, from January 2013 to January 2014. In addition, from 2014 to 2017 Ms. Lawton served as a biotech consultant for various companies, including as Chief Operating Officer consultant at X4 Pharmaceuticals. Ms. Lawton worked at various positions of increasing responsibility at Genzyme Corporation (Genzyme) and subsequently at Sanofi-Aventis, following its 2011 acquisition of Genzyme, each a global biopharmaceutical company. Ms. Lawton served as head of Genzyme Biosurgery, where she was responsible for Genzyme’s global orthopedics, surgical and cell therapy and regenerative medicine businesses. Prior to that, Ms. Lawton oversaw Global Market Access at Genzyme, which included Regulatory Affairs, Global Health Outcomes and Strategic Pricing, Global Public Policy and Global Product Safety & Risk Management. Before joining Genzyme, Ms. Lawton worked for seven years in the United Kingdom at Parke-Davis, a pharmaceutical company. Ms. Lawton serves on the board of directors of ProQR Therapeutics, a public biopharmaceutical company. She also has served on the boards of directors of CoLucid Pharmaceuticals, Inc. until its acquisition by Eli Lilly & Co. and of Cubist Pharmaceuticals until its acquisition by Merck & Co., Inc. She is past President and Chair of the Board of Regulatory Affairs Professional Society and past FDA Advisory Committee member for the Cell and Gene Therapy Committee. She earned her B.Sc. in Pharmacology, with honors, from King’s College London.

高管简历

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Daniel de Boer

Daniel de Boer,2012年2月我公司成立起,他担任创始首席执行官。他是一名信息技术企业家,曾领导多家公司发展、创新发展和多个信息技术相关产品在欧洲多国的推广。加入我公司之前,2009至2011年,他担任RNA Systems的创始人和首席执行官;2007至2008年,担任PC Basic的创始人和首席执行官;2005至2011年,担任Running IT的创始人和首席执行官。他负责公司所有的战略和综合业务。


Daniel de Boer is our founding Chief Executive Officer since our incorporation in 2012. Daniel is a serial-entrepreneur and passionate advocate for rare disease patients. He assembled a group of successful biotech executives as co-founders and built a team of a 150 experienced scientists and drug developers, devoted to creating RNA therapies for patients in need. Under Daniel’s leadership ProQR initiated clinical trials in multiple development programs for rare diseases, and raised over € 300 million in funding, including an IPO on Nasdaq. Daniel is responsible for the overall strategy and general business in the company. Before founding ProQR, Daniel was founder and Chief Executive Officer of RNA Systems, PC Basic and Running IT, companies he led through phases of growth, developing and launching several products in multiple European countries. Daniel was also a co-founder of Amylon Therapeutics, a company developing therapies for genetic brain diseases. In 2018 Daniel was named "Emerging Entrepreneur of the Year" by EY. In 2019 Daniel was selected for the Young Global Leaders program at the World Economic Forum.
Daniel de Boer,2012年2月我公司成立起,他担任创始首席执行官。他是一名信息技术企业家,曾领导多家公司发展、创新发展和多个信息技术相关产品在欧洲多国的推广。加入我公司之前,2009至2011年,他担任RNA Systems的创始人和首席执行官;2007至2008年,担任PC Basic的创始人和首席执行官;2005至2011年,担任Running IT的创始人和首席执行官。他负责公司所有的战略和综合业务。
Daniel de Boer is our founding Chief Executive Officer since our incorporation in 2012. Daniel is a serial-entrepreneur and passionate advocate for rare disease patients. He assembled a group of successful biotech executives as co-founders and built a team of a 150 experienced scientists and drug developers, devoted to creating RNA therapies for patients in need. Under Daniel’s leadership ProQR initiated clinical trials in multiple development programs for rare diseases, and raised over € 300 million in funding, including an IPO on Nasdaq. Daniel is responsible for the overall strategy and general business in the company. Before founding ProQR, Daniel was founder and Chief Executive Officer of RNA Systems, PC Basic and Running IT, companies he led through phases of growth, developing and launching several products in multiple European countries. Daniel was also a co-founder of Amylon Therapeutics, a company developing therapies for genetic brain diseases. In 2018 Daniel was named "Emerging Entrepreneur of the Year" by EY. In 2019 Daniel was selected for the Young Global Leaders program at the World Economic Forum.
Gerard Platenburg

Gerard Platenburg,2014年2月起,他担任我公司首席创新官。他是我公司的创始人之一;2012年8月至2013年12月,曾担任我公司监事会唯一成员。主管我公司创新部门期间,他累计了丰富的核糖核酸调制和罕见药物发现与开发经验。他在成长型生物技术公司担任20多年不同的运营和领导职位,获得了许多高级管理经验。加入我公司之前,2009年6月至2014年1月,他就职于Isa Pharmaceuticals B.V。 他联合成立了Prosensa Holding N.V., 并将其发展为一家知名的核糖核酸调制临床阶段公司;2002年4月至2009年5月,担任多职,包括首席执行官和首席发展官。1990年4月至2002年3月,他就职于Pharming B.V。他是新兴技术充满热情和驱动力的先锋。1987年,他在莱顿大学(Leiden University)获得化学与分子生物学硕士学位,并继续就读博士学位。


Gerard Platenburg has served as our Chief Innovation Officer since February 2014. Mr. Platenburg is a co-founder of our company and also served as the sole member of our supervisory board between August 2012 and December 2013. Mr. Platenburg has an extensive background in RNA modulation and orphan drug discovery and development and is in charge of our innovation unit. Mr. Platenburg has more than twenty years of senior managerial experience, which he gained during his different operational and leadership roles in growing biotech companies. Prior to joining our company, Mr. Platenburg worked at Isa Pharmaceuticals B.V. from June 2009 to January 2014. Mr. Platenburg co-founded Prosensa Holding N.V., growing it to become a well-known RNA modulation clinical stage company, and held various positions between April 2002 and May 2009 including Chief Executive Officer and Chief Development Officer. Mr. Platenburg also worked at Pharming B.V. from April 1990 to March 2002. He is a passionate and driven pioneer of early stage technologies. Mr. Platenburg has a master’s degree in chemistry and molecular biology from Leiden University in 1987 and pursued PhD work at Leiden University.
Gerard Platenburg,2014年2月起,他担任我公司首席创新官。他是我公司的创始人之一;2012年8月至2013年12月,曾担任我公司监事会唯一成员。主管我公司创新部门期间,他累计了丰富的核糖核酸调制和罕见药物发现与开发经验。他在成长型生物技术公司担任20多年不同的运营和领导职位,获得了许多高级管理经验。加入我公司之前,2009年6月至2014年1月,他就职于Isa Pharmaceuticals B.V。 他联合成立了Prosensa Holding N.V., 并将其发展为一家知名的核糖核酸调制临床阶段公司;2002年4月至2009年5月,担任多职,包括首席执行官和首席发展官。1990年4月至2002年3月,他就职于Pharming B.V。他是新兴技术充满热情和驱动力的先锋。1987年,他在莱顿大学(Leiden University)获得化学与分子生物学硕士学位,并继续就读博士学位。
Gerard Platenburg has served as our Chief Innovation Officer since February 2014. Mr. Platenburg is a co-founder of our company and also served as the sole member of our supervisory board between August 2012 and December 2013. Mr. Platenburg has an extensive background in RNA modulation and orphan drug discovery and development and is in charge of our innovation unit. Mr. Platenburg has more than twenty years of senior managerial experience, which he gained during his different operational and leadership roles in growing biotech companies. Prior to joining our company, Mr. Platenburg worked at Isa Pharmaceuticals B.V. from June 2009 to January 2014. Mr. Platenburg co-founded Prosensa Holding N.V., growing it to become a well-known RNA modulation clinical stage company, and held various positions between April 2002 and May 2009 including Chief Executive Officer and Chief Development Officer. Mr. Platenburg also worked at Pharming B.V. from April 1990 to March 2002. He is a passionate and driven pioneer of early stage technologies. Mr. Platenburg has a master’s degree in chemistry and molecular biology from Leiden University in 1987 and pursued PhD work at Leiden University.
David Rodman

David Rodman是我们研发的执行Vice President。David于2017年加入ProQR,此前曾在Novartis Institute for Biomedical Research NIBR,Vertex Pharmaceuticals,Miragen Therapeutics和Nivalis Therapeutics担任领导职务。在2005年转到工业之前,David拥有杰出的学术生涯,领导科罗拉多大学遗传肺部疾病中心,并指导科罗拉多州丹佛市国家犹太医学和研究中心的囊性纤维化护理,教学和研究工作。在工业领域的12年中,David一直负责推动创新,将尖端科学转化为罕见疾病的变革性新疗法,包括CF,肺纤维化,肺动脉高压以及严重的免疫性和炎症性疾病。在Vertex Pharmaceuticals,他指导早期和晚期CF临床开发计划,包括Kalydeco®;,Orkambi®;和VX-661。David于1976年获得Haverford College经济学学士学位,1980年获得University of Pennsylvania医学博士学位,并在University of Colorado完成内科、肺部和重症监护医学培训。他曾担任the National Institutes of Health的顾问,入选美国临床研究学会(the American Society for Clinical Research),是美国心脏协会(the American Heart Association)的院士。


David Rodman is our Executive Vice President of Research & Development. David joined ProQR in 2017 having previously served in leadership roles with Novartis Institutes for Biomedical Research NIBR, Vertex Pharmaceuticals, miRagen Therapeutics and Nivalis Therapeutics. Prior to moving to industry in 2005 David had a distinguished academic career, leading the Center for Genetic Lung Diseases at the University of Colorado and directing the Cystic Fibrosis Care, Teaching and Research efforts at the National Jewish Medical and Research Center in Denver, Colorado. During 12 years in industry, David has had global responsibility for driving innovation in the translation of cutting-edge science into transformational new therapies for rare diseases including CF, pulmonary fibrosis, pulmonary artery hypertension and severe immunologic and inflammatory diseases. At Vertex Pharmaceuticals he directed early- and late-stage CF clinical development programs including Kalydeco®, Orkambi® and VX-661. David received a BA in Economics from Haverford College in 1976 an MD from the University of Pennsylvania in 1980 and completed training in Internal Medicine, Pulmonary and Critical Care Medicine at the University of Colorado. He has served as an advisor to the National Institutes of Health, was elected to the American Society for Clinical Investigation and is a Fellow of the American Heart Association.
David Rodman是我们研发的执行Vice President。David于2017年加入ProQR,此前曾在Novartis Institute for Biomedical Research NIBR,Vertex Pharmaceuticals,Miragen Therapeutics和Nivalis Therapeutics担任领导职务。在2005年转到工业之前,David拥有杰出的学术生涯,领导科罗拉多大学遗传肺部疾病中心,并指导科罗拉多州丹佛市国家犹太医学和研究中心的囊性纤维化护理,教学和研究工作。在工业领域的12年中,David一直负责推动创新,将尖端科学转化为罕见疾病的变革性新疗法,包括CF,肺纤维化,肺动脉高压以及严重的免疫性和炎症性疾病。在Vertex Pharmaceuticals,他指导早期和晚期CF临床开发计划,包括Kalydeco®;,Orkambi®;和VX-661。David于1976年获得Haverford College经济学学士学位,1980年获得University of Pennsylvania医学博士学位,并在University of Colorado完成内科、肺部和重症监护医学培训。他曾担任the National Institutes of Health的顾问,入选美国临床研究学会(the American Society for Clinical Research),是美国心脏协会(the American Heart Association)的院士。
David Rodman is our Executive Vice President of Research & Development. David joined ProQR in 2017 having previously served in leadership roles with Novartis Institutes for Biomedical Research NIBR, Vertex Pharmaceuticals, miRagen Therapeutics and Nivalis Therapeutics. Prior to moving to industry in 2005 David had a distinguished academic career, leading the Center for Genetic Lung Diseases at the University of Colorado and directing the Cystic Fibrosis Care, Teaching and Research efforts at the National Jewish Medical and Research Center in Denver, Colorado. During 12 years in industry, David has had global responsibility for driving innovation in the translation of cutting-edge science into transformational new therapies for rare diseases including CF, pulmonary fibrosis, pulmonary artery hypertension and severe immunologic and inflammatory diseases. At Vertex Pharmaceuticals he directed early- and late-stage CF clinical development programs including Kalydeco®, Orkambi® and VX-661. David received a BA in Economics from Haverford College in 1976 an MD from the University of Pennsylvania in 1980 and completed training in Internal Medicine, Pulmonary and Critical Care Medicine at the University of Colorado. He has served as an advisor to the National Institutes of Health, was elected to the American Society for Clinical Investigation and is a Fellow of the American Heart Association.
Smital Shah

Smital Shah自2019年3月以来一直担任我们的董事会成员。自2014年10月以来,Shah女士一直在ProQR Therapeutics NV(一家罕见疾病公司)担任越来越重要的职务,包括担任首席财务官,最近担任首席业务和财务官。此前,沙阿女士管理着吉利德科学公司数十亿美元的债务、现金和投资组合。任职Gilead公司之前,她曾担任Leerink Partners公司和JP Morgan公司的投资银行家,专注于生物技术领域的资本筹集和战略交易。此前,Shah女士在强生公司公司担任过各种研究与开发职务。她持有孟买大学(the University of Mumbai)的化学工程学士学位、弗吉尼亚理工大学(Virginia Tech)的化学工程硕士学位和加州大学伯克利分校哈斯商学院(the University of Berkeley Haas School of Business)的工商管理硕士学位。


Smital Shah,has served as a member of Graphite Bio, Inc. board of directors since April 2021. Ms. Shah currently serves on the board of directors of Pliant Therapeutics, Inc. (NASDAQ: PLRX) since March 2019. From December 2018 to December 2022, Ms. Shah was the Chief Business and Financial Officer at ProQR Therapeutics NV (NASDAQ: PRQR) and prior to that, she was the company's Chief Financial Officer from October 2014 to December 2018. From August 2012 to September 2014, Ms. Shah was in Corporate Treasury at Gilead Sciences, Inc. (NASDAQ: GILD). Prior to Gilead Sciences, Inc., she was an investment banker at Leerink Partners LLC and JP Morgan Chase and Co., where she focused on capital raising and strategic transactions in the biotechnology space. Ms. Shah also held various research and development roles at Johnson & Johnson Company. Ms. Shah holds a B.S. in Chemical Engineering from the University of Mumbai, a M.S. in Chemical Engineering from Virginia Tech and an M.B.A. from the University of California, Berkeley Haas School of Business.
Smital Shah自2019年3月以来一直担任我们的董事会成员。自2014年10月以来,Shah女士一直在ProQR Therapeutics NV(一家罕见疾病公司)担任越来越重要的职务,包括担任首席财务官,最近担任首席业务和财务官。此前,沙阿女士管理着吉利德科学公司数十亿美元的债务、现金和投资组合。任职Gilead公司之前,她曾担任Leerink Partners公司和JP Morgan公司的投资银行家,专注于生物技术领域的资本筹集和战略交易。此前,Shah女士在强生公司公司担任过各种研究与开发职务。她持有孟买大学(the University of Mumbai)的化学工程学士学位、弗吉尼亚理工大学(Virginia Tech)的化学工程硕士学位和加州大学伯克利分校哈斯商学院(the University of Berkeley Haas School of Business)的工商管理硕士学位。
Smital Shah,has served as a member of Graphite Bio, Inc. board of directors since April 2021. Ms. Shah currently serves on the board of directors of Pliant Therapeutics, Inc. (NASDAQ: PLRX) since March 2019. From December 2018 to December 2022, Ms. Shah was the Chief Business and Financial Officer at ProQR Therapeutics NV (NASDAQ: PRQR) and prior to that, she was the company's Chief Financial Officer from October 2014 to December 2018. From August 2012 to September 2014, Ms. Shah was in Corporate Treasury at Gilead Sciences, Inc. (NASDAQ: GILD). Prior to Gilead Sciences, Inc., she was an investment banker at Leerink Partners LLC and JP Morgan Chase and Co., where she focused on capital raising and strategic transactions in the biotechnology space. Ms. Shah also held various research and development roles at Johnson & Johnson Company. Ms. Shah holds a B.S. in Chemical Engineering from the University of Mumbai, a M.S. in Chemical Engineering from Virginia Tech and an M.B.A. from the University of California, Berkeley Haas School of Business.