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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
William Waddill Independent Director 65 46.73万美元 1.65 2023-01-10
Marianne De Backe Independent Director 54 45.73万美元 未持股 2023-01-10
Adeoye Olukotun Independent Director 78 45.73万美元 未持股 2023-01-10
Victoria Vakiener Independent Director 59 65.88万美元 未持股 2023-01-10
Christopher Anzalone Chief Executive Officer, President & Director 53 1203.20万美元 236.64 2023-01-10
Mauro Ferrari Independent Director 63 45.73万美元 3.97 2023-01-10
Douglass Given Board Chair 70 47.23万美元 21.01 2023-01-10
Michael S. Perry Independent Lead Director 63 45.73万美元 26.20 2023-01-10

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
Patrick O'Brien Chief Operating Officer and General Counsel 59 472.79万美元 26.30 2023-01-10
Javier San Martin Chief Medical Officer 57 65.85万美元 未持股 2023-01-10
James Hamilton Chief of Discovery and Translational Medicine 45 432.33万美元 未持股 2023-01-10
Tracie Oliver Chief Commercial Officer 61 274.45万美元 未持股 2023-01-10
Christopher Anzalone Chief Executive Officer, President & Director 53 1203.20万美元 236.64 2023-01-10
Kenneth A. Myszkowski Chief Financial Officer 56 473.96万美元 40.40 2023-01-10

董事简历

中英对照 |  中文 |  英文
William Waddill

William Waddill的职业生涯始于30年前的商业银行和公共会计,并已在生物技术行业超过25年。自2016年以来,他一直担任Protagonist Therapeutics(位于加利福尼亚州纽瓦克的临床阶段生物制药公司)的董事会成员,最近于2014年至2016年担任临床阶段制药公司Calithera Bioscience的高级副总裁兼首席财务官。加入Calithera之前,Waddill从2007年到2014年担任Oncomed Pharmaceuticals高级副总裁和首席财务官。Waddill先生曾担任生物技术公司Ilypsa,Inc.的高级副总裁兼首席财务官,该公司于2007年被Amgen,Inc.收购。在加入ILYPSA之前,他曾担任Square One Finance(一家金融咨询公司)的创始人和负责人,Waddill先生曾担任Exelixis,Inc.(一家生物技术公司)的财务和行政高级总监。Waddill先生在芝加哥伊利诺伊大学(University of Illinois,Chicago)获得会计学学士学位,并在波士顿普华永道会计师事务所(PricewaterhouseCoopers)和德勤会计师事务所(Deloitte)工作后获得不活跃会计师认证。


William Waddill,began his career over 35 years ago in commercial banking and public accounting and has been in the biotechnology industry for over 30 years. He currently serves on the boards of Protagonist Therapeutics (NASDAQ: PTGX) and Annexon Biosciences (NASDAQ: ANNX), both clinical-stage biopharmaceutical companies. Mr. Waddill was Senior Vice President and CFO of Calithera Bioscience (NASDAQ: CALA), from 2014 to 2016 and Senior Vice President and CFO at OncoMed Pharmaceuticals from 2007 to 2014, both of which were public clinical-stage biopharmaceutical companies. Prior to that, he served as the Senior Vice President and CFO of Ilypsa, Inc., a biotechnology company that was acquired in 2007 by Amgen, Inc. Before joining Ilypsa, he served as the founder and principal at Square One Finance, a financial consulting business. Mr. Waddill received a BS in accounting from the University of Illinois, Chicago, and certification as a public accountant (inactive) after working at PriceWaterhouseCoopers and Deloitte in Boston.
William Waddill的职业生涯始于30年前的商业银行和公共会计,并已在生物技术行业超过25年。自2016年以来,他一直担任Protagonist Therapeutics(位于加利福尼亚州纽瓦克的临床阶段生物制药公司)的董事会成员,最近于2014年至2016年担任临床阶段制药公司Calithera Bioscience的高级副总裁兼首席财务官。加入Calithera之前,Waddill从2007年到2014年担任Oncomed Pharmaceuticals高级副总裁和首席财务官。Waddill先生曾担任生物技术公司Ilypsa,Inc.的高级副总裁兼首席财务官,该公司于2007年被Amgen,Inc.收购。在加入ILYPSA之前,他曾担任Square One Finance(一家金融咨询公司)的创始人和负责人,Waddill先生曾担任Exelixis,Inc.(一家生物技术公司)的财务和行政高级总监。Waddill先生在芝加哥伊利诺伊大学(University of Illinois,Chicago)获得会计学学士学位,并在波士顿普华永道会计师事务所(PricewaterhouseCoopers)和德勤会计师事务所(Deloitte)工作后获得不活跃会计师认证。
William Waddill,began his career over 35 years ago in commercial banking and public accounting and has been in the biotechnology industry for over 30 years. He currently serves on the boards of Protagonist Therapeutics (NASDAQ: PTGX) and Annexon Biosciences (NASDAQ: ANNX), both clinical-stage biopharmaceutical companies. Mr. Waddill was Senior Vice President and CFO of Calithera Bioscience (NASDAQ: CALA), from 2014 to 2016 and Senior Vice President and CFO at OncoMed Pharmaceuticals from 2007 to 2014, both of which were public clinical-stage biopharmaceutical companies. Prior to that, he served as the Senior Vice President and CFO of Ilypsa, Inc., a biotechnology company that was acquired in 2007 by Amgen, Inc. Before joining Ilypsa, he served as the founder and principal at Square One Finance, a financial consulting business. Mr. Waddill received a BS in accounting from the University of Illinois, Chicago, and certification as a public accountant (inactive) after working at PriceWaterhouseCoopers and Deloitte in Boston.
Marianne De Backe

Marianne De Backe自2019年起担任Bayer AG Bayry Pharmaceuticals Division的执行委员会成员,执行Vice President以及战略,业务发展和许可主管。她也是Gladstone Foundation的董事会成员,以及Stanford-Bayer Digital Advisory Board的顾问成员。此前,从1991年到2018年,她曾任职强生公司,在那里她最近担任全球业务和企业发展职务,包括制药集团全球并购运营和资产剥离Vice President和传染病与疫苗业务开发主管。此前,她曾领导欧洲的商业业务部门,以及欧洲和美国的药物发现研究。de Backer博士拥有鹿特丹伊拉斯谟大学(Erasmus University Rotterdam)的工商管理硕士学位,布鲁塞尔Vrije大学(Vrije Universiteit Brussels)的分子生物学和生物技术硕士学位,根特大学(Ghent University)的工程硕士学位和生物技术博士学位。


Marianne De Backe,brings over 25 years of international experience in healthcare, biotechnology, innovation, strategy, business and corporate development. She has served as member of the Executive Committee, Executive Vice President and Head of Strategy, Business Development and Licensing, and Open Innovation of the pharmaceuticals division of Bayer AG (BAYRY) since 2019. She also serves on the board of directors of Gladstone Foundation, and Bayer-acquired companies Bluerock Therapeutics, AskBio, and Vividion Therapeutics. Previously, from 1991 through 2018, she was at Johnson & Johnson (NYSE: JNJ) where she most recently held global Corporate Development and Venture Investor roles including the position of Global Vice President of M&A Operations and Divestitures globally for the Pharmaceuticals Group and head of Infectious Diseases & Vaccines Business Development. Prior to that she led a commercial business unit in Europe as well as drug discovery research teams in both Europe and the United States. In 2022, Dr. De Backer was recognized by BCG and Manager Magazin as one of the 100 Most Influential Women in German business and Top 25 Women Leaders in Biotechnology by Healthcare Technology Report. In 2021, she was named one of the Fiercest Women in Life Sciences by Fierce Pharma. Dr. De Backer holds an MBA from Erasmus University Rotterdam, a Master's degree in Molecular Biology and Biotechnology from Vrije Universiteit Brussels, and a Master's degree in Engineering and a PhD in Biotechnology from Ghent University.On January 25, 2023 it was announced that Dr. De Backer was appointed as Chief Executive Officer of Vir Biotechnology, Inc., effective as of April 3, 2023. Dr. De Backer will also join Vir's board of directors, effective as of April 3, 2023. Subsequently, on January 26, 2023, it was announced that Dr. De Backer will resign as board member of Kronos Bio, Inc., effective likely in the first or second quarter of 2023.
Marianne De Backe自2019年起担任Bayer AG Bayry Pharmaceuticals Division的执行委员会成员,执行Vice President以及战略,业务发展和许可主管。她也是Gladstone Foundation的董事会成员,以及Stanford-Bayer Digital Advisory Board的顾问成员。此前,从1991年到2018年,她曾任职强生公司,在那里她最近担任全球业务和企业发展职务,包括制药集团全球并购运营和资产剥离Vice President和传染病与疫苗业务开发主管。此前,她曾领导欧洲的商业业务部门,以及欧洲和美国的药物发现研究。de Backer博士拥有鹿特丹伊拉斯谟大学(Erasmus University Rotterdam)的工商管理硕士学位,布鲁塞尔Vrije大学(Vrije Universiteit Brussels)的分子生物学和生物技术硕士学位,根特大学(Ghent University)的工程硕士学位和生物技术博士学位。
Marianne De Backe,brings over 25 years of international experience in healthcare, biotechnology, innovation, strategy, business and corporate development. She has served as member of the Executive Committee, Executive Vice President and Head of Strategy, Business Development and Licensing, and Open Innovation of the pharmaceuticals division of Bayer AG (BAYRY) since 2019. She also serves on the board of directors of Gladstone Foundation, and Bayer-acquired companies Bluerock Therapeutics, AskBio, and Vividion Therapeutics. Previously, from 1991 through 2018, she was at Johnson & Johnson (NYSE: JNJ) where she most recently held global Corporate Development and Venture Investor roles including the position of Global Vice President of M&A Operations and Divestitures globally for the Pharmaceuticals Group and head of Infectious Diseases & Vaccines Business Development. Prior to that she led a commercial business unit in Europe as well as drug discovery research teams in both Europe and the United States. In 2022, Dr. De Backer was recognized by BCG and Manager Magazin as one of the 100 Most Influential Women in German business and Top 25 Women Leaders in Biotechnology by Healthcare Technology Report. In 2021, she was named one of the Fiercest Women in Life Sciences by Fierce Pharma. Dr. De Backer holds an MBA from Erasmus University Rotterdam, a Master's degree in Molecular Biology and Biotechnology from Vrije Universiteit Brussels, and a Master's degree in Engineering and a PhD in Biotechnology from Ghent University.On January 25, 2023 it was announced that Dr. De Backer was appointed as Chief Executive Officer of Vir Biotechnology, Inc., effective as of April 3, 2023. Dr. De Backer will also join Vir's board of directors, effective as of April 3, 2023. Subsequently, on January 26, 2023, it was announced that Dr. De Backer will resign as board member of Kronos Bio, Inc., effective likely in the first or second quarter of 2023.
Adeoye Olukotun

Adeoye Olukotun于2018年9月成为董事。Olukotun博士自2000年以来一直担任医疗产品咨询公司CR Strategies,LLC的首席执行官,并于2014年至2018年1月担任制药公司Epigen Pharmaceuticals,Inc.的首席执行官。Olukotun博士于2012年至2016年担任制药公司Cardovax,Inc.的副董事长,并于2006年至2012年担任其首席执行官。他还是制药公司Via Pharmaceuticals,Inc.的联合创始人,从2004年到2008年担任该公司的首席医疗官。


Adeoye Olukotun,is a Mayo Clinic trained cardiologist who has served as Chief Executive Officer of CR Strategies, LLC, which consults on clinical trial design and FDA strategy for pharmaceutical development , since 2001. Dr. Olukotun currently serves on the board of directors of Tonix Pharmaceuticals Holding Corp. (NASDAQ: TNXP), a clinical-stage biopharmaceuticals company. He served as CEO of Epigen Pharmaceuticals, Inc., a discovery phase biotechnology company, from 2014 to 2017, and Vice Board Chair of CardioVax, Inc., a clinical-stage biopharmaceutical company, from 2012 to 2016. He spent the first 20 years of his career in roles of increasing responsibility in clinical development, including multiple product approvals, at Pfizer, Bristol-Myers Squibb, and Mallinckrodt. He has over 35 years of experience in the pharmaceutical industry and has been instrumental in the approval and success of numerous cardiology and metabolic medicines, including the first daily beta blocker and the first approved ACE inhibitor, among others. Dr. Olukotun received his Medical Doctor degree from the Albert Einstein College of Medicine in New York, and a Masters in Public Health from Harvard University School of Public Health.
Adeoye Olukotun于2018年9月成为董事。Olukotun博士自2000年以来一直担任医疗产品咨询公司CR Strategies,LLC的首席执行官,并于2014年至2018年1月担任制药公司Epigen Pharmaceuticals,Inc.的首席执行官。Olukotun博士于2012年至2016年担任制药公司Cardovax,Inc.的副董事长,并于2006年至2012年担任其首席执行官。他还是制药公司Via Pharmaceuticals,Inc.的联合创始人,从2004年到2008年担任该公司的首席医疗官。
Adeoye Olukotun,is a Mayo Clinic trained cardiologist who has served as Chief Executive Officer of CR Strategies, LLC, which consults on clinical trial design and FDA strategy for pharmaceutical development , since 2001. Dr. Olukotun currently serves on the board of directors of Tonix Pharmaceuticals Holding Corp. (NASDAQ: TNXP), a clinical-stage biopharmaceuticals company. He served as CEO of Epigen Pharmaceuticals, Inc., a discovery phase biotechnology company, from 2014 to 2017, and Vice Board Chair of CardioVax, Inc., a clinical-stage biopharmaceutical company, from 2012 to 2016. He spent the first 20 years of his career in roles of increasing responsibility in clinical development, including multiple product approvals, at Pfizer, Bristol-Myers Squibb, and Mallinckrodt. He has over 35 years of experience in the pharmaceutical industry and has been instrumental in the approval and success of numerous cardiology and metabolic medicines, including the first daily beta blocker and the first approved ACE inhibitor, among others. Dr. Olukotun received his Medical Doctor degree from the Albert Einstein College of Medicine in New York, and a Masters in Public Health from Harvard University School of Public Health.
Victoria Vakiener

Victoria Vakiener目前在Chimerix(纳斯达克股票代码:CMRX)的董事会任职,该公司是一家临床阶段的生物制药公司。从2018年11月到2021年9月,她在Epizyme, Inc.担任首席商务官,该公司是一家生物制药公司,于2022年被收购,她在那里建立了商业机构,并在六个月内推出了TAZVERIK用于两个适应症。在加入Epizyme之前,Vakiener女士在强生公司(纽约证券交易所代码:JNJ)担任了20多年的高管,在该公司担任领导职务,在公司的制药和诊断业务中承担着越来越大的责任。Vakiener女士的制药生涯始于Schering-Plough,在那里她从事了九年的科学和商业工作。Vakiener女士在奥尔布赖特学院获得生物化学学士学位。


Victoria Vakiener,currently serves on the board of directors of Chimerix (NASDAQ: CMRX), a clinical-stage biopharmaceutical company. From November 2018 through September 2021, she served as Chief Commercial Officer of Epizyme, Inc., a biopharmaceutical company that was acquired in 2022, where she built the commercial organization and launched TAZVERIK for two indications within six months. Prior to joining Epizyme, Ms. Vakiener was an executive at Johnson & Johnson (NYSE: JNJ) for more than twenty years where she held positions of leadership with increasing responsibility across the company's pharmaceutical and diagnostics businesses. Ms. Vakiener began her pharmaceutical career at Schering-Plough, where she spent nine years in both scientific and commercial roles. Ms. Vakiener received a BS in Biochemistry from Albright College.
Victoria Vakiener目前在Chimerix(纳斯达克股票代码:CMRX)的董事会任职,该公司是一家临床阶段的生物制药公司。从2018年11月到2021年9月,她在Epizyme, Inc.担任首席商务官,该公司是一家生物制药公司,于2022年被收购,她在那里建立了商业机构,并在六个月内推出了TAZVERIK用于两个适应症。在加入Epizyme之前,Vakiener女士在强生公司(纽约证券交易所代码:JNJ)担任了20多年的高管,在该公司担任领导职务,在公司的制药和诊断业务中承担着越来越大的责任。Vakiener女士的制药生涯始于Schering-Plough,在那里她从事了九年的科学和商业工作。Vakiener女士在奥尔布赖特学院获得生物化学学士学位。
Victoria Vakiener,currently serves on the board of directors of Chimerix (NASDAQ: CMRX), a clinical-stage biopharmaceutical company. From November 2018 through September 2021, she served as Chief Commercial Officer of Epizyme, Inc., a biopharmaceutical company that was acquired in 2022, where she built the commercial organization and launched TAZVERIK for two indications within six months. Prior to joining Epizyme, Ms. Vakiener was an executive at Johnson & Johnson (NYSE: JNJ) for more than twenty years where she held positions of leadership with increasing responsibility across the company's pharmaceutical and diagnostics businesses. Ms. Vakiener began her pharmaceutical career at Schering-Plough, where she spent nine years in both scientific and commercial roles. Ms. Vakiener received a BS in Biochemistry from Albright College.
Christopher Anzalone

Christopher Anzalone, 2007年12月1日,他成为公司的总裁、首席执行官及董事。2005年,Anzalone博士在Benet Group LLC公司担任首席执行官。Benet Group LLC是一家创建纳米生物科技公司的私募股权公司。在Benet集团工作期间,他是两家投资组合公司Nanotope公司(一家研究组织再生的公司)和Leonardo Biosystems公司(一家癌症药物递送公司)的创业总裁。他是Arrowhead公司全资控股子公司Arrowhead Madison 公司和多数控股子公司Calando 制药、Ablaris Therapeutics公司、Tego Biosciences公司,以及少数投资公司Leonardo Biosystems的董事。1999年至2003年,他是华盛顿特区私人股本公司Galway Partners, LLC的合伙人。他在该公司负责采购、组织和建立新企业。他是NanoInk公司(一家领先的纳米公司)的创业总裁。他在加州大学洛杉矶分校获得生物学博士学位;在劳伦斯大学获得管理学学士学位。


Christopher Anzalone,has been President, Chief Executive Officer and Director of the Company since December 1, 2007 and has led the Company's business and technical development since then. Prior to joining Arrowhead, Dr. Anzalone formed and served as CEO of the Benet Group LLC, a private equity firm focused on creating and building new nano-biotechnology companies from university-generated science. Prior to his tenure at the Benet Group, from 1999 until 2003, he was a partner at the Washington, DC-based private equity firm Galway Partners, LLC, where he was responsible for sourcing, structuring and building new business ventures. Dr. Anzalone holds a PhD. in Biology from UCLA and a B.A. in Government from Lawrence University.
Christopher Anzalone, 2007年12月1日,他成为公司的总裁、首席执行官及董事。2005年,Anzalone博士在Benet Group LLC公司担任首席执行官。Benet Group LLC是一家创建纳米生物科技公司的私募股权公司。在Benet集团工作期间,他是两家投资组合公司Nanotope公司(一家研究组织再生的公司)和Leonardo Biosystems公司(一家癌症药物递送公司)的创业总裁。他是Arrowhead公司全资控股子公司Arrowhead Madison 公司和多数控股子公司Calando 制药、Ablaris Therapeutics公司、Tego Biosciences公司,以及少数投资公司Leonardo Biosystems的董事。1999年至2003年,他是华盛顿特区私人股本公司Galway Partners, LLC的合伙人。他在该公司负责采购、组织和建立新企业。他是NanoInk公司(一家领先的纳米公司)的创业总裁。他在加州大学洛杉矶分校获得生物学博士学位;在劳伦斯大学获得管理学学士学位。
Christopher Anzalone,has been President, Chief Executive Officer and Director of the Company since December 1, 2007 and has led the Company's business and technical development since then. Prior to joining Arrowhead, Dr. Anzalone formed and served as CEO of the Benet Group LLC, a private equity firm focused on creating and building new nano-biotechnology companies from university-generated science. Prior to his tenure at the Benet Group, from 1999 until 2003, he was a partner at the Washington, DC-based private equity firm Galway Partners, LLC, where he was responsible for sourcing, structuring and building new business ventures. Dr. Anzalone holds a PhD. in Biology from UCLA and a B.A. in Government from Lawrence University.
Mauro Ferrari

Mauro Ferrari目前担任Washington州西雅图的华盛顿大学药剂学副教授以及德克萨斯州休斯顿的BrYet Pharmaceutics的首席执行官。从2010年到2019年,Ferrari博士曾在Houston Methodist医院担任多个不同职务,包括Houston Methodist医院研究所(TMHRI)总裁兼首席执行官、Houston Methodist医院执行副总裁以及该医院学术附属机构纽约威尔康奈尔医学院的高级副院长。Ferrari博士是国际公认的癌症治疗、纳米医学和生物医学纳米技术专家。他之前的学术任命包括在他毕业的母校加州大学伯克利分校、俄亥俄州立大学担任终身教授,在德克萨斯大学健康科学中心担任纳米医学和生物医学工程系教授和系主任,在MD安德森癌症中心担任实验治疗教授,并在莱斯大学担任生物工程兼职教授。2003年至2005年,Ferrari博士在国家癌症研究所担任纳米技术特别专家和著名学者。他获得了许多国家和国际奖项和表彰。


Mauro Ferrari,currently serves as Affiliate Professor of Pharmaceutics at the University of Washington in Seattle, Washington and as CEO of BrYet Pharmaceutics in Houston, Texas. From 2010 to 2019, Dr. Ferrari served in several different capacities at the Houston Methodist Hospital, including President and CEO of The Houston Methodist Hospital Research Institute (TMHRI), Executive Vice President of Houston Methodist Hospital, and Senior Associate Dean of the hospital's academic affiliate, Weill Cornell Medical College in New York. Dr. Ferrari is an internationally recognized expert in cancer therapeutics, nanomedicine and biomedical nanotechnology. His previous academic appointments include tenured professorships at his graduate Alma Mater UC Berkeley, The Ohio State University, as Professor and Chair of The Department of NanoMedicine and Biomedical Engineering at The University of Texas Health Science Center, Professor of Experimental Therapeutics at the MD Anderson Cancer Center, and Adjunct Professor of Bioengineering at Rice University. From 2003 to 2005, Dr. Ferrari served as Special Expert on Nanotechnology and Eminent Scholar at The National Cancer Institute. He has received many National and International awards and recognitions.
Mauro Ferrari目前担任Washington州西雅图的华盛顿大学药剂学副教授以及德克萨斯州休斯顿的BrYet Pharmaceutics的首席执行官。从2010年到2019年,Ferrari博士曾在Houston Methodist医院担任多个不同职务,包括Houston Methodist医院研究所(TMHRI)总裁兼首席执行官、Houston Methodist医院执行副总裁以及该医院学术附属机构纽约威尔康奈尔医学院的高级副院长。Ferrari博士是国际公认的癌症治疗、纳米医学和生物医学纳米技术专家。他之前的学术任命包括在他毕业的母校加州大学伯克利分校、俄亥俄州立大学担任终身教授,在德克萨斯大学健康科学中心担任纳米医学和生物医学工程系教授和系主任,在MD安德森癌症中心担任实验治疗教授,并在莱斯大学担任生物工程兼职教授。2003年至2005年,Ferrari博士在国家癌症研究所担任纳米技术特别专家和著名学者。他获得了许多国家和国际奖项和表彰。
Mauro Ferrari,currently serves as Affiliate Professor of Pharmaceutics at the University of Washington in Seattle, Washington and as CEO of BrYet Pharmaceutics in Houston, Texas. From 2010 to 2019, Dr. Ferrari served in several different capacities at the Houston Methodist Hospital, including President and CEO of The Houston Methodist Hospital Research Institute (TMHRI), Executive Vice President of Houston Methodist Hospital, and Senior Associate Dean of the hospital's academic affiliate, Weill Cornell Medical College in New York. Dr. Ferrari is an internationally recognized expert in cancer therapeutics, nanomedicine and biomedical nanotechnology. His previous academic appointments include tenured professorships at his graduate Alma Mater UC Berkeley, The Ohio State University, as Professor and Chair of The Department of NanoMedicine and Biomedical Engineering at The University of Texas Health Science Center, Professor of Experimental Therapeutics at the MD Anderson Cancer Center, and Adjunct Professor of Bioengineering at Rice University. From 2003 to 2005, Dr. Ferrari served as Special Expert on Nanotechnology and Eminent Scholar at The National Cancer Institute. He has received many National and International awards and recognitions.
Douglass Given

Douglass Given, 2010年11月,成为公司董事。2000年10月,他成为美国生命科学风险资本公司(Bay City Capital)的投资合伙人。他是NeoRx, Corporate Sr。公司的前任首席执行官兼董事,是万灵科(Mallinckrodt)公司的首席技术官兼副总裁,是Progenitor and Mercator Genetics公司的首席执行官兼董事。他是先灵葆雅研究所(Schering-Plough Research Institute)的副总裁;是Monsanto(孟山都公司)G.D. Searle研究实验室的副总裁;也是礼来研究实验室(Lilly research laboratories)的副总裁。Given博士是Vivaldi Biosciences生物科技公司的主席。该公司是一家私营的风险资本支持的生物科技公司。2007年至2013年, 他在芝加哥大学的普利兹克医学院的生物科学学部的访查委员会任职,并且是该委员会的终身成员及杰出校友奖的获得者。他是the Johns Hopkins Bloomberg 学校的公共卫生咨询委员会成员、是哈佛大学公共卫生部的成员、是南加州大学斯蒂文斯理工学院咨询委员会的成员。他以优异的成绩获得了芝加哥大学的硕士学位,博士学位。他还获得了宾夕法尼亚大学的沃顿商学院的工商管理硕士学位。他是哈佛大学医学院及马萨诸塞州综合医院的内科及传染病研究员。


Douglass Given,has been Managing Partner at Health2047 Capital Partners LLC, a healthcare-focused venture capital firm, since 2018. He served as Health2047 lnc.'s Chief Executive Officer from its founding in 2015 until 2018. Dr. Given has spent more than two decades in venture capital as an Investment Partner and General Partner at life sciences investor Bay City Capital LLC participating in five sequential life sciences general funds and two sector-specific funds; he was associated with the partnership from 1999-2015. Dr. Given is a physician and medical scientist. Since 1983, he has been a global corporate and operating executive at Lilly, Monsanto, Schering Plough and Mallinckrodt, and a serial entrepreneur. In addition to a number of private companies, Dr. Given led three public biopharmaceutical companies as CEO.Dr. Given has served on more than 20 public and private boards. He is currently Arrowhead Pharmaceuticals, Inc. Board Chair, a Director at Health2047 Inc., Managing Partner at GS Partners LLC, and serves on the board at First Mile Care Inc, BrYet Health Ltd, Visirna Therapeutics, and Vivaldi Biosciences Inc. He serves in advisory roles on the University of Chicago Pritzker School of Medicine, and Biological Sciences Division Council (former Chair), Johns Hopkins Bloomberg School of Public Health, Health Advisory Board. Dr. Given received MD and PhD degrees from the University of Chicago, a MBA from the Wharton School at the University of Pennsylvania, and was a Clinical and Research Fellow in internal medicine and infectious diseases at Massachusetts General Hospital and Harvard Medical School.
Douglass Given, 2010年11月,成为公司董事。2000年10月,他成为美国生命科学风险资本公司(Bay City Capital)的投资合伙人。他是NeoRx, Corporate Sr。公司的前任首席执行官兼董事,是万灵科(Mallinckrodt)公司的首席技术官兼副总裁,是Progenitor and Mercator Genetics公司的首席执行官兼董事。他是先灵葆雅研究所(Schering-Plough Research Institute)的副总裁;是Monsanto(孟山都公司)G.D. Searle研究实验室的副总裁;也是礼来研究实验室(Lilly research laboratories)的副总裁。Given博士是Vivaldi Biosciences生物科技公司的主席。该公司是一家私营的风险资本支持的生物科技公司。2007年至2013年, 他在芝加哥大学的普利兹克医学院的生物科学学部的访查委员会任职,并且是该委员会的终身成员及杰出校友奖的获得者。他是the Johns Hopkins Bloomberg 学校的公共卫生咨询委员会成员、是哈佛大学公共卫生部的成员、是南加州大学斯蒂文斯理工学院咨询委员会的成员。他以优异的成绩获得了芝加哥大学的硕士学位,博士学位。他还获得了宾夕法尼亚大学的沃顿商学院的工商管理硕士学位。他是哈佛大学医学院及马萨诸塞州综合医院的内科及传染病研究员。
Douglass Given,has been Managing Partner at Health2047 Capital Partners LLC, a healthcare-focused venture capital firm, since 2018. He served as Health2047 lnc.'s Chief Executive Officer from its founding in 2015 until 2018. Dr. Given has spent more than two decades in venture capital as an Investment Partner and General Partner at life sciences investor Bay City Capital LLC participating in five sequential life sciences general funds and two sector-specific funds; he was associated with the partnership from 1999-2015. Dr. Given is a physician and medical scientist. Since 1983, he has been a global corporate and operating executive at Lilly, Monsanto, Schering Plough and Mallinckrodt, and a serial entrepreneur. In addition to a number of private companies, Dr. Given led three public biopharmaceutical companies as CEO.Dr. Given has served on more than 20 public and private boards. He is currently Arrowhead Pharmaceuticals, Inc. Board Chair, a Director at Health2047 Inc., Managing Partner at GS Partners LLC, and serves on the board at First Mile Care Inc, BrYet Health Ltd, Visirna Therapeutics, and Vivaldi Biosciences Inc. He serves in advisory roles on the University of Chicago Pritzker School of Medicine, and Biological Sciences Division Council (former Chair), Johns Hopkins Bloomberg School of Public Health, Health Advisory Board. Dr. Given received MD and PhD degrees from the University of Chicago, a MBA from the Wharton School at the University of Pennsylvania, and was a Clinical and Research Fellow in internal medicine and infectious diseases at Massachusetts General Hospital and Harvard Medical School.
Michael S. Perry

Michael S. Perry, 2011年12月,加入Arrowhead公司董事会。他在诺华制药公司的干细胞疗法研究的全球总监。2005年至2012年11月,在诺华制药任职之前,他是Bay City Capital LLP公司的投资合伙人。2010年至2012年11月, 他是Poniard制药公司的首席医学官。他现任AmpliPhi Biosciences Corporation APHB.PK 公司和Avita Medical (ASX:AVH and OTCQX:AVMXY)公司的董事。2005年4月至2009年5月,他是VIA制药公司的首席开发官。该公司一家药品研发的上市公司。在那之前,2003年6月至2005年4月,他是 Extropy制药公司的主席兼首席执行官。该公司是一家私营儿科专业制药公司。2002年至2003年,Perry博士担任Baxter 生物科学公司研发部门的全球总监。1997年至2000年,他是SyStemix Inc. 公司和 Genetic Therapy Inc.公司的总裁兼首席执行官。两家公司都是诺华集团的全资子公司。1994年至1997年,他是诺华制药(前身是Sandoz 制药)的法规事务的副总裁。1994年之前,他在辛泰克公司 (Syntex Corporation)、先灵葆雅公司(Schering-Plough Corporation)和BioResearch Laboratories, Inc公司担任过多个管理职务。Perry博士在加拿大安大略省圭而夫大学获得了动物医学博士学位、生物医药理学博士学位、物理学学士学位。他毕业于哈佛商学院国际管理项目系。


Michael S. Perry,is currently a Venture Partner with Bioscience Managers, a global venture capital firm. He also serves as Chairman and board member of 7 Hills Pharma, a private clinical stage pharmaceutical company. Dr. Perry was Chief Executive Officer of Avita Medical, Inc., a regenerative medicine company based in Valencia, CA (NASDAQ: RCEL) from 2017 to 2022. From 2014 to 2017, he served as Chief Scientific Officer of Novartis' Cell and Gene Therapy Unit, and from 2012 to 2014 he served as Vice President and Global Head of Stem Cell Therapy for Novartis Pharmaceuticals Corp, the US affiliate of Switzerland-based Novartis AG, a global pharmaceutical company. Dr. Perry has also served as SVP and Global Head of R&D at Baxter Healthcare, President and as CEO of Cell & Gene Therapy at Novartis AG. Earlier in his career he served as VP Regulatory Affairs at Novartis, Sandoz Pharmaceuticals, and Syntex Corporation. He also served as Director of Regulatory Affairs at Schering-Plough Corporation. Dr. Perry also served as a Venture Partner with Bay City Capital, LLC for eight years. Dr. Perry has previously served as a board member for the following companies: Ampliphi Bioscience Corp, Gamida Cell Ltd, Targeted Genetics, Inc., American Xeno, Inc., BioTransplant, Inc., ltamar Biomedical Ltd, Systemix, Inc., Genetic Therapy, Inc., Extropy Pharmaceuticals, Inc, and Pharsight Corporation. Dr. Perry holds an Honors Bachelor of Science in Physics and Engineering and a PhD in Biomedical Pharmacology from the University of Guelph. He also holds a Doctor of Veterinary Medicine & Surgery from Ontario Veterinary College and is a graduate of the International Advanced Management Program at Harvard Business School. Dr. Perry currently serves as Adjunct Professor at the Gates Center for Regenerative Medicine at the University of Colorado Anschutz Medical Campus and as Faculty at Houston Methodist and Chair of the Translational Medicine Advisory Board of the Houston Methodist Research Institute.
Michael S. Perry, 2011年12月,加入Arrowhead公司董事会。他在诺华制药公司的干细胞疗法研究的全球总监。2005年至2012年11月,在诺华制药任职之前,他是Bay City Capital LLP公司的投资合伙人。2010年至2012年11月, 他是Poniard制药公司的首席医学官。他现任AmpliPhi Biosciences Corporation APHB.PK 公司和Avita Medical (ASX:AVH and OTCQX:AVMXY)公司的董事。2005年4月至2009年5月,他是VIA制药公司的首席开发官。该公司一家药品研发的上市公司。在那之前,2003年6月至2005年4月,他是 Extropy制药公司的主席兼首席执行官。该公司是一家私营儿科专业制药公司。2002年至2003年,Perry博士担任Baxter 生物科学公司研发部门的全球总监。1997年至2000年,他是SyStemix Inc. 公司和 Genetic Therapy Inc.公司的总裁兼首席执行官。两家公司都是诺华集团的全资子公司。1994年至1997年,他是诺华制药(前身是Sandoz 制药)的法规事务的副总裁。1994年之前,他在辛泰克公司 (Syntex Corporation)、先灵葆雅公司(Schering-Plough Corporation)和BioResearch Laboratories, Inc公司担任过多个管理职务。Perry博士在加拿大安大略省圭而夫大学获得了动物医学博士学位、生物医药理学博士学位、物理学学士学位。他毕业于哈佛商学院国际管理项目系。
Michael S. Perry,is currently a Venture Partner with Bioscience Managers, a global venture capital firm. He also serves as Chairman and board member of 7 Hills Pharma, a private clinical stage pharmaceutical company. Dr. Perry was Chief Executive Officer of Avita Medical, Inc., a regenerative medicine company based in Valencia, CA (NASDAQ: RCEL) from 2017 to 2022. From 2014 to 2017, he served as Chief Scientific Officer of Novartis' Cell and Gene Therapy Unit, and from 2012 to 2014 he served as Vice President and Global Head of Stem Cell Therapy for Novartis Pharmaceuticals Corp, the US affiliate of Switzerland-based Novartis AG, a global pharmaceutical company. Dr. Perry has also served as SVP and Global Head of R&D at Baxter Healthcare, President and as CEO of Cell & Gene Therapy at Novartis AG. Earlier in his career he served as VP Regulatory Affairs at Novartis, Sandoz Pharmaceuticals, and Syntex Corporation. He also served as Director of Regulatory Affairs at Schering-Plough Corporation. Dr. Perry also served as a Venture Partner with Bay City Capital, LLC for eight years. Dr. Perry has previously served as a board member for the following companies: Ampliphi Bioscience Corp, Gamida Cell Ltd, Targeted Genetics, Inc., American Xeno, Inc., BioTransplant, Inc., ltamar Biomedical Ltd, Systemix, Inc., Genetic Therapy, Inc., Extropy Pharmaceuticals, Inc, and Pharsight Corporation. Dr. Perry holds an Honors Bachelor of Science in Physics and Engineering and a PhD in Biomedical Pharmacology from the University of Guelph. He also holds a Doctor of Veterinary Medicine & Surgery from Ontario Veterinary College and is a graduate of the International Advanced Management Program at Harvard Business School. Dr. Perry currently serves as Adjunct Professor at the Gates Center for Regenerative Medicine at the University of Colorado Anschutz Medical Campus and as Faculty at Houston Methodist and Chair of the Translational Medicine Advisory Board of the Houston Methodist Research Institute.

高管简历

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Patrick O'Brien

Patrick O'Brien 是总法律顾问,于2014年12月加入本公司。O'Brien先生在医疗保健法律领域开展法律执业超过20年。加入该公司以前,从2012年到2014年,O'Brien先生在Shire任职,他在该公司担任法律部的事业部副总裁。在Shire工作前,他担任国际律师事务所Holland & Knight LLP华盛顿特区办事处的合伙人。O'Brien先生于2010年与人合作创始律所O’Brien Gould PLLC,该公司于2011年与Holland & Knight合并。从2009年至2010年,O'Brien先生是 Burke O'Neil LLC的合伙人。从2001年到2009年,O'Brien先生担任强生公司(Johnson & Johnson)的几个法律职位,包括担任J&J&'s Centocor 奥托生物技术单位的法律部副总裁。在这之前,O'Brien先生担任美国食品药品监督管理局(United States Food & Drug Administration)的监管法律顾问。O'Brien先生在亚利桑那大学(University of Arizona)被授予药学理学学士学位和药学博士学位,之后在伊利诺伊大学(University of Illinois)芝加哥医院(Chicago Hospital)完成临床药学住院医师实习。他还在亚利桑那大学(University of Arizona)被授予法学博士学位。


Patrick O'Brien,Chief Operating Officer and General Counsel, joined the Company in December 2014, where he has served as Chief Operating Officer since July 2022 and as General Counsel since 2014. Mr. O'Brien has practiced in the healthcare legal field for over 30 years. Before joining the Company, from 2012 to 2014, Mr. O'Brien was with Shire, as global pharmaceutical company, where he was Group Vice President, Law. Immediately prior to working with Shire he was a partner with the international law firm of Holland & Knight LLP in its Washington, DC office. In 2010, Mr. O'Brien co-founded the law firm O'Brien Gould PLLC which joined Holland & Knight in 2011. From 2009 to 2010, Mr. O'Brien was a partner in Burke O'Neil LLC. From 2001 to 2009, Mr. O'Brien served in several legal roles with Johnson & Johnson, including serving as Vice President of Law for J&J's Centocor Ortho-Biotech unit. Mr. O'Brien previously served as Regulatory Counsel with the United States Food & Drug Administration. Mr. O'Brien was awarded a BS in Pharmacy and a PharmD from the University of Arizona before completing a residency in Clinical Pharmacy with the University of Illinois at Chicago Hospital. He was also awarded his JD from the University of Arizona.
Patrick O'Brien 是总法律顾问,于2014年12月加入本公司。O'Brien先生在医疗保健法律领域开展法律执业超过20年。加入该公司以前,从2012年到2014年,O'Brien先生在Shire任职,他在该公司担任法律部的事业部副总裁。在Shire工作前,他担任国际律师事务所Holland & Knight LLP华盛顿特区办事处的合伙人。O'Brien先生于2010年与人合作创始律所O’Brien Gould PLLC,该公司于2011年与Holland & Knight合并。从2009年至2010年,O'Brien先生是 Burke O'Neil LLC的合伙人。从2001年到2009年,O'Brien先生担任强生公司(Johnson & Johnson)的几个法律职位,包括担任J&J&'s Centocor 奥托生物技术单位的法律部副总裁。在这之前,O'Brien先生担任美国食品药品监督管理局(United States Food & Drug Administration)的监管法律顾问。O'Brien先生在亚利桑那大学(University of Arizona)被授予药学理学学士学位和药学博士学位,之后在伊利诺伊大学(University of Illinois)芝加哥医院(Chicago Hospital)完成临床药学住院医师实习。他还在亚利桑那大学(University of Arizona)被授予法学博士学位。
Patrick O'Brien,Chief Operating Officer and General Counsel, joined the Company in December 2014, where he has served as Chief Operating Officer since July 2022 and as General Counsel since 2014. Mr. O'Brien has practiced in the healthcare legal field for over 30 years. Before joining the Company, from 2012 to 2014, Mr. O'Brien was with Shire, as global pharmaceutical company, where he was Group Vice President, Law. Immediately prior to working with Shire he was a partner with the international law firm of Holland & Knight LLP in its Washington, DC office. In 2010, Mr. O'Brien co-founded the law firm O'Brien Gould PLLC which joined Holland & Knight in 2011. From 2009 to 2010, Mr. O'Brien was a partner in Burke O'Neil LLC. From 2001 to 2009, Mr. O'Brien served in several legal roles with Johnson & Johnson, including serving as Vice President of Law for J&J's Centocor Ortho-Biotech unit. Mr. O'Brien previously served as Regulatory Counsel with the United States Food & Drug Administration. Mr. O'Brien was awarded a BS in Pharmacy and a PharmD from the University of Arizona before completing a residency in Clinical Pharmacy with the University of Illinois at Chicago Hospital. He was also awarded his JD from the University of Arizona.
Javier San Martin

Javier San Martin,首席医疗官,于2019年11月加入公司。San Martin博士曾于2013年至2019年11月担任Ultragenyx的高级副总裁兼全球临床开发主管。在Ultragenyx,他领导了Burosumab(一种治疗X连锁低磷血症的新药,在包括美国、欧盟和加拿大在内的主要地区获得批准)的开发。任职Ultragenyx公司之前,他曾担任Alder Biopharmaceuticals公司的临床开发高级副总裁,在那里他负责管理专注于早期临床项目的医疗、监管和临床运营集团。从2006年到2011年,他曾担任Amgen公司的全球开发领导,在那里他曾负责两个主要开发计划。他指导the Romosozumab Clinical Program直到II期结束,在此之前,负责DeNosumab的开发和批准,DeNosumab是最大的品牌抗骨质疏松治疗绝经后骨质疏松症的药物,也是第一个针对初级保健医生治疗的非常流行的疾病的单克隆抗体。任职Amgen公司之前,他曾任职礼来公司公司7年,支持后期临床开发和医疗事务活动,包括Evista公司和Forteo公司的成功上市。他在布宜诺斯艾利斯大学医学院(University of Buenos Aires Medical School)获得医学学位,并在阿根廷布宜诺斯艾利斯CEMC University Hospital完成内科住院,担任首席住院医师,此后担任主治医师,负责内科病房。


Javier San Martin,Chief Medical Officer, joined the Company in November 2019. Dr. San Martin previously served as Senior Vice President and Head of Global Clinical Development at Ultragenyx from 2013 until November 2019. At Ultragenyx he led the development of burosumab, a novel drug for the treatment of X-Linked Hypophosphatemia approved across major regions including the United States, the European Union, and Canada. Before his tenure at Ultragenyx, he served as Senior Vice President of Clinical Development at Alder Biopharmaceuticals, where he was responsible for managing the medical, regulatory, and clinical operations group focused on early clinical programs. From 2006 to 2011, Dr. San Martin was a Global Development Leader at Amgen, Inc., where he was responsible for two major development programs. He directed the romosozumab clinical program through the end of phase II, and before that, was responsible for the development and approval of denosumab, the largest branded anti-osteoporosis treatment for postmenopausal osteoporosis and the first monoclonal antibody to address a very prevalent disease treated by primary care physicians. Prior to his time at Amgen, he spent seven years at Eli Lilly and Company, supporting late stage clinical development as well as medical affairs activities, including the successful launch of Evista and Forteo. He received his medical degree from the University of Buenos Aires Medical School and completed his residence in internal medicine at CEMIC University Hospital in Buenos Aires, Argentina, serving as Chief Resident, and, thereafter, as Attending Physician responsible for the internal medicine ward.
Javier San Martin,首席医疗官,于2019年11月加入公司。San Martin博士曾于2013年至2019年11月担任Ultragenyx的高级副总裁兼全球临床开发主管。在Ultragenyx,他领导了Burosumab(一种治疗X连锁低磷血症的新药,在包括美国、欧盟和加拿大在内的主要地区获得批准)的开发。任职Ultragenyx公司之前,他曾担任Alder Biopharmaceuticals公司的临床开发高级副总裁,在那里他负责管理专注于早期临床项目的医疗、监管和临床运营集团。从2006年到2011年,他曾担任Amgen公司的全球开发领导,在那里他曾负责两个主要开发计划。他指导the Romosozumab Clinical Program直到II期结束,在此之前,负责DeNosumab的开发和批准,DeNosumab是最大的品牌抗骨质疏松治疗绝经后骨质疏松症的药物,也是第一个针对初级保健医生治疗的非常流行的疾病的单克隆抗体。任职Amgen公司之前,他曾任职礼来公司公司7年,支持后期临床开发和医疗事务活动,包括Evista公司和Forteo公司的成功上市。他在布宜诺斯艾利斯大学医学院(University of Buenos Aires Medical School)获得医学学位,并在阿根廷布宜诺斯艾利斯CEMC University Hospital完成内科住院,担任首席住院医师,此后担任主治医师,负责内科病房。
Javier San Martin,Chief Medical Officer, joined the Company in November 2019. Dr. San Martin previously served as Senior Vice President and Head of Global Clinical Development at Ultragenyx from 2013 until November 2019. At Ultragenyx he led the development of burosumab, a novel drug for the treatment of X-Linked Hypophosphatemia approved across major regions including the United States, the European Union, and Canada. Before his tenure at Ultragenyx, he served as Senior Vice President of Clinical Development at Alder Biopharmaceuticals, where he was responsible for managing the medical, regulatory, and clinical operations group focused on early clinical programs. From 2006 to 2011, Dr. San Martin was a Global Development Leader at Amgen, Inc., where he was responsible for two major development programs. He directed the romosozumab clinical program through the end of phase II, and before that, was responsible for the development and approval of denosumab, the largest branded anti-osteoporosis treatment for postmenopausal osteoporosis and the first monoclonal antibody to address a very prevalent disease treated by primary care physicians. Prior to his time at Amgen, he spent seven years at Eli Lilly and Company, supporting late stage clinical development as well as medical affairs activities, including the successful launch of Evista and Forteo. He received his medical degree from the University of Buenos Aires Medical School and completed his residence in internal medicine at CEMIC University Hospital in Buenos Aires, Argentina, serving as Chief Resident, and, thereafter, as Attending Physician responsible for the internal medicine ward.
James Hamilton

James Hamilton,高级副总裁,发现与转化医学,于2014年加入该公司。他负责目标发现以及非临床和早期临床开发。此前,Hamilton博士曾担任临床开发Vice President,负责临床策略、临床试验设计和执行,包括所有箭头项目的早期转化和中期开发。他在多个疾病领域经验丰富,包括病毒学、肝脏学、心血管疾病、罕见病和肿瘤学。Hamilton博士领导ARO-HBV(现为JNJ-3989)的临床开发,该公司已获得Janssen Pharmaceuticals的许可。与此同时,Hamilton博士曾担任公司开发主管,并领导Novartis&8217;RNAi Assets的Arrowhead&8217;s许可交易,以及ARO-LPA(现为AMG890)向Amgen的许可以及ARO-AAT与武田的合作伙伴关系。Hamilton博士在箭头公司(Arrowhead)开始任职,担任医疗总监和企业发展主管。他持有俄亥俄州立大学(the Ohio State University)的医学博士和工商管理硕士学位。他是一名有执照的医生,并完成了急诊医学的董事会认证的住院医师培训。


James Hamilton,Chief of Discovery & Translational Medicine, joined the Company in 2014. He is responsible for target discovery as well as non-clinical and early clinical development. Previously, Dr. Hamilton served as Vice President, Clinical Development, responsible for clinical strategy, clinical trial design and execution including early translational and mid-stage development of all Arrowhead programs. He is experienced in multiple disease areas including virology, hepatology, cardiovascular disease, rare disease and oncology. Dr. Hamilton led the clinical development of ARO-HBV (now JNJ-3989), which was licensed to Janssen Pharmaceuticals. In parallel, Dr. Hamilton served as Head of Corporate Development and led Arrowhead's in-licensing transaction of Novartis's RNAi assets, as well as the out-licensing of ARO-LPA (now AMG890) to Amgen and the ARO-AAT partnership with Takeda. Dr. Hamilton started his employment at Arrowhead as Medical Director and Head of Corporate development. He holds both MD and MBA degrees from The Ohio State University. He is a licensed physician and completed residency training with board certification in emergency medicine.
James Hamilton,高级副总裁,发现与转化医学,于2014年加入该公司。他负责目标发现以及非临床和早期临床开发。此前,Hamilton博士曾担任临床开发Vice President,负责临床策略、临床试验设计和执行,包括所有箭头项目的早期转化和中期开发。他在多个疾病领域经验丰富,包括病毒学、肝脏学、心血管疾病、罕见病和肿瘤学。Hamilton博士领导ARO-HBV(现为JNJ-3989)的临床开发,该公司已获得Janssen Pharmaceuticals的许可。与此同时,Hamilton博士曾担任公司开发主管,并领导Novartis&8217;RNAi Assets的Arrowhead&8217;s许可交易,以及ARO-LPA(现为AMG890)向Amgen的许可以及ARO-AAT与武田的合作伙伴关系。Hamilton博士在箭头公司(Arrowhead)开始任职,担任医疗总监和企业发展主管。他持有俄亥俄州立大学(the Ohio State University)的医学博士和工商管理硕士学位。他是一名有执照的医生,并完成了急诊医学的董事会认证的住院医师培训。
James Hamilton,Chief of Discovery & Translational Medicine, joined the Company in 2014. He is responsible for target discovery as well as non-clinical and early clinical development. Previously, Dr. Hamilton served as Vice President, Clinical Development, responsible for clinical strategy, clinical trial design and execution including early translational and mid-stage development of all Arrowhead programs. He is experienced in multiple disease areas including virology, hepatology, cardiovascular disease, rare disease and oncology. Dr. Hamilton led the clinical development of ARO-HBV (now JNJ-3989), which was licensed to Janssen Pharmaceuticals. In parallel, Dr. Hamilton served as Head of Corporate Development and led Arrowhead's in-licensing transaction of Novartis's RNAi assets, as well as the out-licensing of ARO-LPA (now AMG890) to Amgen and the ARO-AAT partnership with Takeda. Dr. Hamilton started his employment at Arrowhead as Medical Director and Head of Corporate development. He holds both MD and MBA degrees from The Ohio State University. He is a licensed physician and completed residency training with board certification in emergency medicine.
Tracie Oliver

首席商务官Tracie Oliver于2022年6月加入Arrowhead。Oliver女士在生物制药行业拥有30多年的全球经验,领导研发和商业组织。在加入Arrowhead之前,她有自己的咨询业务,自2019年起专注于为小型生物技术公司制定商业和发展战略。她于2016年通过收购Baxalta加入夏尔制药,并在2019年之前担任新产品规划和设备战略全球主管。在此之前,她曾在百特和Baxalta担任过多个商业职务,包括建立一个新的肿瘤专营权,领导北美免疫学事业部和自身免疫专营权。Oliver女士的职业生涯始于强生公司的生物制药行业,曾担任加拿大Ortho Biotech Nephrology业务部、美国Ortho McNeil Neurologics和McNeil Pediatrics的负责人,并领导了一家内部企业,开发用于急性缺血性中风的同种异体细胞疗法。她在安大略省金斯敦皇后大学获得学士和理学硕士学位,在多伦多约克大学舒立克商学院获得工商管理硕士学位。


Tracie Oliver,Chief Commercial Officer, joined Arrowhead in June 2022. Ms. Oliver has over 30 years of global experience in the biopharmaceutical industry leading both R&D and Commercial organizations. Prior to joining Arrowhead, she had her own consulting practice focused on development of commercial and development strategy for small biotech companies since 2019. She joined Shire Pharmaceuticals in 2016 through the acquisition of Baxalta and was Global Head of New Product Planning and Device Strategy until 2019. Prior to that she held several commercial roles at Baxter and Baxalta including establishing a new oncology franchise and leading the North America Immunology Business Unit and Autoimmune Franchise. Ms. Oliver began her career in the biopharmaceutical industry with Johnson & Johnson and served as head of Ortho Biotech Nephrology Business Unit in Canada, Ortho McNeil Neurologics, and McNeil Pediatrics in the USA and led an internal venture developing an allogeneic cell therapy for acute ischemic stroke. She received her BSc and MSc from Queen's University in Kingston, Ontario and her MBA from the Shulich School of Business, York University, Toronto.
首席商务官Tracie Oliver于2022年6月加入Arrowhead。Oliver女士在生物制药行业拥有30多年的全球经验,领导研发和商业组织。在加入Arrowhead之前,她有自己的咨询业务,自2019年起专注于为小型生物技术公司制定商业和发展战略。她于2016年通过收购Baxalta加入夏尔制药,并在2019年之前担任新产品规划和设备战略全球主管。在此之前,她曾在百特和Baxalta担任过多个商业职务,包括建立一个新的肿瘤专营权,领导北美免疫学事业部和自身免疫专营权。Oliver女士的职业生涯始于强生公司的生物制药行业,曾担任加拿大Ortho Biotech Nephrology业务部、美国Ortho McNeil Neurologics和McNeil Pediatrics的负责人,并领导了一家内部企业,开发用于急性缺血性中风的同种异体细胞疗法。她在安大略省金斯敦皇后大学获得学士和理学硕士学位,在多伦多约克大学舒立克商学院获得工商管理硕士学位。
Tracie Oliver,Chief Commercial Officer, joined Arrowhead in June 2022. Ms. Oliver has over 30 years of global experience in the biopharmaceutical industry leading both R&D and Commercial organizations. Prior to joining Arrowhead, she had her own consulting practice focused on development of commercial and development strategy for small biotech companies since 2019. She joined Shire Pharmaceuticals in 2016 through the acquisition of Baxalta and was Global Head of New Product Planning and Device Strategy until 2019. Prior to that she held several commercial roles at Baxter and Baxalta including establishing a new oncology franchise and leading the North America Immunology Business Unit and Autoimmune Franchise. Ms. Oliver began her career in the biopharmaceutical industry with Johnson & Johnson and served as head of Ortho Biotech Nephrology Business Unit in Canada, Ortho McNeil Neurologics, and McNeil Pediatrics in the USA and led an internal venture developing an allogeneic cell therapy for acute ischemic stroke. She received her BSc and MSc from Queen's University in Kingston, Ontario and her MBA from the Shulich School of Business, York University, Toronto.
Christopher Anzalone

Christopher Anzalone, 2007年12月1日,他成为公司的总裁、首席执行官及董事。2005年,Anzalone博士在Benet Group LLC公司担任首席执行官。Benet Group LLC是一家创建纳米生物科技公司的私募股权公司。在Benet集团工作期间,他是两家投资组合公司Nanotope公司(一家研究组织再生的公司)和Leonardo Biosystems公司(一家癌症药物递送公司)的创业总裁。他是Arrowhead公司全资控股子公司Arrowhead Madison 公司和多数控股子公司Calando 制药、Ablaris Therapeutics公司、Tego Biosciences公司,以及少数投资公司Leonardo Biosystems的董事。1999年至2003年,他是华盛顿特区私人股本公司Galway Partners, LLC的合伙人。他在该公司负责采购、组织和建立新企业。他是NanoInk公司(一家领先的纳米公司)的创业总裁。他在加州大学洛杉矶分校获得生物学博士学位;在劳伦斯大学获得管理学学士学位。


Christopher Anzalone,has been President, Chief Executive Officer and Director of the Company since December 1, 2007 and has led the Company's business and technical development since then. Prior to joining Arrowhead, Dr. Anzalone formed and served as CEO of the Benet Group LLC, a private equity firm focused on creating and building new nano-biotechnology companies from university-generated science. Prior to his tenure at the Benet Group, from 1999 until 2003, he was a partner at the Washington, DC-based private equity firm Galway Partners, LLC, where he was responsible for sourcing, structuring and building new business ventures. Dr. Anzalone holds a PhD. in Biology from UCLA and a B.A. in Government from Lawrence University.
Christopher Anzalone, 2007年12月1日,他成为公司的总裁、首席执行官及董事。2005年,Anzalone博士在Benet Group LLC公司担任首席执行官。Benet Group LLC是一家创建纳米生物科技公司的私募股权公司。在Benet集团工作期间,他是两家投资组合公司Nanotope公司(一家研究组织再生的公司)和Leonardo Biosystems公司(一家癌症药物递送公司)的创业总裁。他是Arrowhead公司全资控股子公司Arrowhead Madison 公司和多数控股子公司Calando 制药、Ablaris Therapeutics公司、Tego Biosciences公司,以及少数投资公司Leonardo Biosystems的董事。1999年至2003年,他是华盛顿特区私人股本公司Galway Partners, LLC的合伙人。他在该公司负责采购、组织和建立新企业。他是NanoInk公司(一家领先的纳米公司)的创业总裁。他在加州大学洛杉矶分校获得生物学博士学位;在劳伦斯大学获得管理学学士学位。
Christopher Anzalone,has been President, Chief Executive Officer and Director of the Company since December 1, 2007 and has led the Company's business and technical development since then. Prior to joining Arrowhead, Dr. Anzalone formed and served as CEO of the Benet Group LLC, a private equity firm focused on creating and building new nano-biotechnology companies from university-generated science. Prior to his tenure at the Benet Group, from 1999 until 2003, he was a partner at the Washington, DC-based private equity firm Galway Partners, LLC, where he was responsible for sourcing, structuring and building new business ventures. Dr. Anzalone holds a PhD. in Biology from UCLA and a B.A. in Government from Lawrence University.
Kenneth A. Myszkowski

Kenneth A. Myszkowski, 2009年加入Arrowhead公司,担任该公司的首席财务官。加入Arrowhead公司之前,他是Broadwind Energy公司的财务总监。Broadwind Energy公司是一家为风力发电产业提供商产品及服务的上市公司。在Broadwind Energy公司任职之前,他是Epcor USA公司的Epcor Utilities, Inc美国总部的财务总监。该公司是一家能源上市公司。加入Epcor之前,他是两个初创企业NanoInk,公司(专门从事纳米蘸水笔技术和纳米组装技术研发的公司)和Delphion公司(为知识产权研究提供在线工具的公司)的财务总监。Myszkowski先生在FMC Corporation(美国富美实公司及Premark International公司的担任过多种职务,两家公司均是财富500强企业。他在伊利诺斯州芝加哥市的Arthur Andersen & Co公司审计实务开始他的职业生涯。他在伊利诺斯大学获得了本科学士学位,在芝加哥大学布斯商学院获得了工商管理硕士。他是一名注册公共会计师。


Kenneth A. Myszkowski,Chief Financial Officer, joined the Company in 2009. Prior to joining Arrowhead, Mr. Myszkowski served as the corporate controller for Broadwind Energy, a public energy company which provides products and services to the wind energy industry. Previous to his position at Broadwind, Mr. Myszkowski was controller for Epcor USA, the U.S. headquarters for Epcor Utilities, Inc., a public energy company. Prior to Epcor, Mr. Myszkowski was controller for two start-up ventures: NanoInk, specializing in Dip Pen Nanolithography, a nanofabrication technology, and Delphion, which provided on-line tools for intellectual property research. Mr. Myszkowski also held several corporate roles at FMC Corporation and Premark International, both Fortune 500 conglomerates. He began his career in the audit practice of Arthur Andersen & Co. in Chicago, Illinois. Mr. Myszkowski received his undergraduate degree from the University of Illinois, and his MBA from the University of Chicago Booth School of Business. He is a certified public accountant.
Kenneth A. Myszkowski, 2009年加入Arrowhead公司,担任该公司的首席财务官。加入Arrowhead公司之前,他是Broadwind Energy公司的财务总监。Broadwind Energy公司是一家为风力发电产业提供商产品及服务的上市公司。在Broadwind Energy公司任职之前,他是Epcor USA公司的Epcor Utilities, Inc美国总部的财务总监。该公司是一家能源上市公司。加入Epcor之前,他是两个初创企业NanoInk,公司(专门从事纳米蘸水笔技术和纳米组装技术研发的公司)和Delphion公司(为知识产权研究提供在线工具的公司)的财务总监。Myszkowski先生在FMC Corporation(美国富美实公司及Premark International公司的担任过多种职务,两家公司均是财富500强企业。他在伊利诺斯州芝加哥市的Arthur Andersen & Co公司审计实务开始他的职业生涯。他在伊利诺斯大学获得了本科学士学位,在芝加哥大学布斯商学院获得了工商管理硕士。他是一名注册公共会计师。
Kenneth A. Myszkowski,Chief Financial Officer, joined the Company in 2009. Prior to joining Arrowhead, Mr. Myszkowski served as the corporate controller for Broadwind Energy, a public energy company which provides products and services to the wind energy industry. Previous to his position at Broadwind, Mr. Myszkowski was controller for Epcor USA, the U.S. headquarters for Epcor Utilities, Inc., a public energy company. Prior to Epcor, Mr. Myszkowski was controller for two start-up ventures: NanoInk, specializing in Dip Pen Nanolithography, a nanofabrication technology, and Delphion, which provided on-line tools for intellectual property research. Mr. Myszkowski also held several corporate roles at FMC Corporation and Premark International, both Fortune 500 conglomerates. He began his career in the audit practice of Arthur Andersen & Co. in Chicago, Illinois. Mr. Myszkowski received his undergraduate degree from the University of Illinois, and his MBA from the University of Chicago Booth School of Business. He is a certified public accountant.