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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
Adrian M. Senderowicz Director 53 49.01万美元 未持股 2017-04-28
Frank E. Zavrl Director 51 49.01万美元 未持股 2017-04-28
Jay M. Moyes Director 63 29.64万美元 未持股 2017-04-28
Alan H. Auerbach President, Chief Executive Officer and Chairman of the Board 47 1085.77万美元 未持股 2017-04-28
Troy E. Wilson Director 48 29.64万美元 未持股 2017-04-28

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
Robert Charnas Senior Vice President, Regulatory Affairs and Project Management 63 366.35万美元 未持股 2017-04-28
Steven Lo Chief Commercial Officer 50 308.12万美元 未持股 2017-04-28
Charles R. Eyler Senior Vice President, Finance and Administration and Treasurer 69 182.54万美元 未持股 2017-04-28
Richard P. Bryce Senior Vice President, Clinical Research and Development 59 323.93万美元 未持股 2017-04-28
Alan H. Auerbach President, Chief Executive Officer and Chairman of the Board 47 1085.77万美元 未持股 2017-04-28

董事简历

中英对照 |  中文 |  英文
Adrian M. Senderowicz

Adrian M. Senderowicz, M.D.,2015年9月以来,他担任我们首席医疗官和高级副总裁。加入Cerulean之前,他担任Ignyta, Inc.(一个公共精密肿瘤生物科技公司)的职务。从2014年8月到2015年2月,他担任临床开发和管理事务的首席医疗官和高级副总裁。从2015年2月到2015年4月,他担任临床和管理战略官。此前从2013年9月到2014年8月,他曾是Sanofi(生物制药公司)的全球监管肿瘤学副总裁。从2012年8月到2013年3月,他担任Tokai Pharmaceuticals, Inc.(生物制药公司,从事前列腺癌治疗)的首席医疗官。从2008年8月到2012年3月,他担任AstraZeneca(全球生物制药公司)的职务并不断被提拔,包括最后担任肿瘤临床开发的高级医学主管。在AstraZeneca任职之前,他担任美国食品和药物管理局的肿瘤药物产品药物评价和研究中心( the U.S. Food and Drug Administration Division of Oncology Drug Products in the Center for Drug Evaluation and Research )的各种领导职务。他担任the National Cancer Institute/National Institutes of Health NCI的各种临床和研究职位,包括分子治疗部门调查员和首席官员。他目前担任Puma Biotechnology, Inc.(上市的生物制药公司)的董事。他在Mount Sinai的the Icahn School of Medicine完成内科住院医师培训。他获得the NCI临床肿瘤学奖学金。他获得阿根廷的 the Universidad de Buenos Aires的医学院的医学博士学位。


Adrian M. Senderowicz, M.D. has served as our Senior Vice President and Chief Medical Officer since September 2015 prior to which he provided consulting services to Cerulean from May 2015 until the commencement of his employment with us. Dr. Senderowicz was Chief Medical Officer and Senior Vice President, Clinical Development and Regulatory Affairs at Ignyta, Inc., a precision oncology biotechnology company, where he served from 2014 to 2015. Prior to joining Ignyta, he served as Vice President, Global Regulatory Oncology at Sanofi from 2013 to 2014 Chief Medical Officer at Tokai Pharmaceuticals from 2012 to 2013 and Senior Medical Director, Oncology Clinical Development at AstraZeneca from 2008 to 2012. Before his tenure at AstraZeneca, Dr. Senderowicz held a variety of leadership positions at the U.S. Food and Drug Administration Division of Oncology Drug Products in the Center for Drug Evaluation and Research and a variety of clinical and research positions with the National Cancer Institute/National Institutes of Health, or NCI, including Investigator and Chief, Molecular Therapeutics Unit. He currently serves as a member of the board of directors of Puma Biotechnology, Inc., a publicly traded biopharmaceutical company. He completed his internal medicine residency training at the Icahn School of Medicine at Mount Sinai, and a clinical oncology fellowship at the NCI. Dr. Senderowicz holds an M.D. from the School of Medicine at the Universidad de Buenos Aires in Argentina.
Adrian M. Senderowicz, M.D.,2015年9月以来,他担任我们首席医疗官和高级副总裁。加入Cerulean之前,他担任Ignyta, Inc.(一个公共精密肿瘤生物科技公司)的职务。从2014年8月到2015年2月,他担任临床开发和管理事务的首席医疗官和高级副总裁。从2015年2月到2015年4月,他担任临床和管理战略官。此前从2013年9月到2014年8月,他曾是Sanofi(生物制药公司)的全球监管肿瘤学副总裁。从2012年8月到2013年3月,他担任Tokai Pharmaceuticals, Inc.(生物制药公司,从事前列腺癌治疗)的首席医疗官。从2008年8月到2012年3月,他担任AstraZeneca(全球生物制药公司)的职务并不断被提拔,包括最后担任肿瘤临床开发的高级医学主管。在AstraZeneca任职之前,他担任美国食品和药物管理局的肿瘤药物产品药物评价和研究中心( the U.S. Food and Drug Administration Division of Oncology Drug Products in the Center for Drug Evaluation and Research )的各种领导职务。他担任the National Cancer Institute/National Institutes of Health NCI的各种临床和研究职位,包括分子治疗部门调查员和首席官员。他目前担任Puma Biotechnology, Inc.(上市的生物制药公司)的董事。他在Mount Sinai的the Icahn School of Medicine完成内科住院医师培训。他获得the NCI临床肿瘤学奖学金。他获得阿根廷的 the Universidad de Buenos Aires的医学院的医学博士学位。
Adrian M. Senderowicz, M.D. has served as our Senior Vice President and Chief Medical Officer since September 2015 prior to which he provided consulting services to Cerulean from May 2015 until the commencement of his employment with us. Dr. Senderowicz was Chief Medical Officer and Senior Vice President, Clinical Development and Regulatory Affairs at Ignyta, Inc., a precision oncology biotechnology company, where he served from 2014 to 2015. Prior to joining Ignyta, he served as Vice President, Global Regulatory Oncology at Sanofi from 2013 to 2014 Chief Medical Officer at Tokai Pharmaceuticals from 2012 to 2013 and Senior Medical Director, Oncology Clinical Development at AstraZeneca from 2008 to 2012. Before his tenure at AstraZeneca, Dr. Senderowicz held a variety of leadership positions at the U.S. Food and Drug Administration Division of Oncology Drug Products in the Center for Drug Evaluation and Research and a variety of clinical and research positions with the National Cancer Institute/National Institutes of Health, or NCI, including Investigator and Chief, Molecular Therapeutics Unit. He currently serves as a member of the board of directors of Puma Biotechnology, Inc., a publicly traded biopharmaceutical company. He completed his internal medicine residency training at the Icahn School of Medicine at Mount Sinai, and a clinical oncology fellowship at the NCI. Dr. Senderowicz holds an M.D. from the School of Medicine at the Universidad de Buenos Aires in Argentina.
Frank E. Zavrl

Frank E. Zavrl,2015年9月以来,他一直担任董事。他曾担任Adage Capital Management, L.P。 的合伙人(2002年至2011年),专注于生物技术投资。加入Adage Capital公司之前,他曾担任Merlin Biomed(医疗投资集团)的投资组合经理(1999年至2002年)。1998年至1999年,他曾担任Scudder Kemper Investments Inc.的分析师,专注于生物技术投资。他持有加州大学伯克利分校(the University of California, Berkeley)的生物化学学士学位,以及达特茅斯学院(Dartmouth College)的塔克商学院的工商管理硕士学位。


Frank E. Zavrl has been a director since September 2015. Mr. Zavrl served as a Partner at Adage Capital Management, L.P. from 2002 to 2011 specializing in biotechnology investments. Prior to joining Adage Capital, Mr. Zavrl was a Portfolio Manager from 1999 to 2002 at Merlin Biomed, a healthcare investment group. From 1998 to 1999 Mr. Zavrl was an analyst at Scudder Kemper Investments Inc., focusing on biotechnology investments. Mr. Zavrl received a B.S. in Biochemistry from the University of California, Berkeley and an M.B.A. from the Tuck School of Business at Dartmouth College.
Frank E. Zavrl,2015年9月以来,他一直担任董事。他曾担任Adage Capital Management, L.P。 的合伙人(2002年至2011年),专注于生物技术投资。加入Adage Capital公司之前,他曾担任Merlin Biomed(医疗投资集团)的投资组合经理(1999年至2002年)。1998年至1999年,他曾担任Scudder Kemper Investments Inc.的分析师,专注于生物技术投资。他持有加州大学伯克利分校(the University of California, Berkeley)的生物化学学士学位,以及达特茅斯学院(Dartmouth College)的塔克商学院的工商管理硕士学位。
Frank E. Zavrl has been a director since September 2015. Mr. Zavrl served as a Partner at Adage Capital Management, L.P. from 2002 to 2011 specializing in biotechnology investments. Prior to joining Adage Capital, Mr. Zavrl was a Portfolio Manager from 1999 to 2002 at Merlin Biomed, a healthcare investment group. From 1998 to 1999 Mr. Zavrl was an analyst at Scudder Kemper Investments Inc., focusing on biotechnology investments. Mr. Zavrl received a B.S. in Biochemistry from the University of California, Berkeley and an M.B.A. from the Tuck School of Business at Dartmouth College.
Jay M. Moyes

Jay M. Moyes,自2006年8月本公司首次公开发行结束之时起,担任董事。他从2012年11月起,担任医疗器械公司Amedica Corporation的董事;2013年10月起,担任其首席财务官。2012年4月,他加入Puma Biotechnology(纽交所代码: PBYI)的董事会,现任其薪酬委员会主席、企业治理委员会主席、审核委员会成员。


Jay M. Moyes,has served on Biocardia, Inc. board of directors since 2011. Mr. Moyes is the Chief Financial Officer of Sera Prognostics, Inc., a women's health diagnostics company, and has served in that capacity since March 2020. He has served on the board of directors and as Chairman of the Audit Committee of Puma Biotechnologies from April 2012 to present, on the board of directors and Chairman of the Audit Committee of Achieve Life Sciences from August 2017 to the present, on the board of directors of Predictive Technology Group, Inc. from February 2019 until December 2019 and on the board of directors and Chairman of the Audit Committee of Osiris Therapeutics, a biosurgical company, from May 2006 until December 2017. He also served as a member of the board of directors and Chairman of the Audit Committee of Integrated Diagnostics, a privately held molecular diagnostics company, from 2011 to 2016. From 2012 to 2014, Mr. Moyes served as a member of the board of directors of Amedica Corporation, a publicly traded orthopaedics company, and as Chief Financial Officer from 2013 to 2014. From 2008 to 2009, Mr. Moyes served as Chief Financial Officer of CareDx, a publicly traded molecular diagnostics company. Prior to that, he served as Chief Financial Officer of Myriad Genetics, Inc., a publicly held healthcare diagnostics company, from June 1996 until his retirement in November 2007, and as Vice President of Finance from July 1993 until July 2005. From 1991 to 1993, Mr. Moyes served as Vice President of Finance and Chief Financial Officer of Genmark, a privately held genetics company. Mr. Moyes held various positions with the accounting firm of KPMG from 1979 to 1991. He also served as a member of the Board of Trustees of the Utah Life Science Association from 1999 to 2006. Mr. Moyes holds a Masters of Business Administration from the University of Utah, a Bachelor of Arts in economics from Weber State University, and was formerly a Certified Public Accountant.
Jay M. Moyes,自2006年8月本公司首次公开发行结束之时起,担任董事。他从2012年11月起,担任医疗器械公司Amedica Corporation的董事;2013年10月起,担任其首席财务官。2012年4月,他加入Puma Biotechnology(纽交所代码: PBYI)的董事会,现任其薪酬委员会主席、企业治理委员会主席、审核委员会成员。
Jay M. Moyes,has served on Biocardia, Inc. board of directors since 2011. Mr. Moyes is the Chief Financial Officer of Sera Prognostics, Inc., a women's health diagnostics company, and has served in that capacity since March 2020. He has served on the board of directors and as Chairman of the Audit Committee of Puma Biotechnologies from April 2012 to present, on the board of directors and Chairman of the Audit Committee of Achieve Life Sciences from August 2017 to the present, on the board of directors of Predictive Technology Group, Inc. from February 2019 until December 2019 and on the board of directors and Chairman of the Audit Committee of Osiris Therapeutics, a biosurgical company, from May 2006 until December 2017. He also served as a member of the board of directors and Chairman of the Audit Committee of Integrated Diagnostics, a privately held molecular diagnostics company, from 2011 to 2016. From 2012 to 2014, Mr. Moyes served as a member of the board of directors of Amedica Corporation, a publicly traded orthopaedics company, and as Chief Financial Officer from 2013 to 2014. From 2008 to 2009, Mr. Moyes served as Chief Financial Officer of CareDx, a publicly traded molecular diagnostics company. Prior to that, he served as Chief Financial Officer of Myriad Genetics, Inc., a publicly held healthcare diagnostics company, from June 1996 until his retirement in November 2007, and as Vice President of Finance from July 1993 until July 2005. From 1991 to 1993, Mr. Moyes served as Vice President of Finance and Chief Financial Officer of Genmark, a privately held genetics company. Mr. Moyes held various positions with the accounting firm of KPMG from 1979 to 1991. He also served as a member of the Board of Trustees of the Utah Life Science Association from 1999 to 2006. Mr. Moyes holds a Masters of Business Administration from the University of Utah, a Bachelor of Arts in economics from Weber State University, and was formerly a Certified Public Accountant.
Alan H. Auerbach

Alan H. Auerbach,2011年5月起,他担任我公司董事会成员,2010年10月至合并,担任Former Operating Company董事会成员。他目前是彪马生物技术公司(Puma Biotechnology, Inc.)的创始人、首席执行官、总裁和董事会主席, 该公司成立于2010年,开发治疗癌症的药物并获得进口许可。2003年5月,他成立Cougar Biotechnology,担任首席执行官、总裁和董事会成员直到2009年7月;2009年7月至2010年1月,担任强生旗下Cougar集成指导委员会共同主席。他在波士顿大学(Boston University)获得生物医学工程学士学位,在南加利福尼亚大学(University of Southern California)获得生物医学工程硕士学位。


Alan H. Auerbach has served on our Board since May 2011 and served as a member of the Board of Directors of our predecessor company from October 2010 until May 2011. Mr. Auerbach is currently the Founder, Chief Executive Officer, President and Chairman of the Board of Directors of Puma Biotechnology, Inc., a company dedicated to in-licensing and developing drugs for the treatment of cancer. Previously, Mr. Auerbach founded Cougar Biotechnology “Cougar”, a biotechnology company, in May 2003 and served as the company’s Chief Executive Officer, President and as a member of its Board of Directors until July 2009. From July 2009 until January 2010 Mr. Auerbach served as the Co-Chairman of the Integration Steering Committee at Cougar after its acquisition by Johnson & Johnson. Mr. Auerbach received a B.S. in Biomedical Engineering from Boston University and an M.S. in Biomedical Engineering from the University of Southern California.
Alan H. Auerbach,2011年5月起,他担任我公司董事会成员,2010年10月至合并,担任Former Operating Company董事会成员。他目前是彪马生物技术公司(Puma Biotechnology, Inc.)的创始人、首席执行官、总裁和董事会主席, 该公司成立于2010年,开发治疗癌症的药物并获得进口许可。2003年5月,他成立Cougar Biotechnology,担任首席执行官、总裁和董事会成员直到2009年7月;2009年7月至2010年1月,担任强生旗下Cougar集成指导委员会共同主席。他在波士顿大学(Boston University)获得生物医学工程学士学位,在南加利福尼亚大学(University of Southern California)获得生物医学工程硕士学位。
Alan H. Auerbach has served on our Board since May 2011 and served as a member of the Board of Directors of our predecessor company from October 2010 until May 2011. Mr. Auerbach is currently the Founder, Chief Executive Officer, President and Chairman of the Board of Directors of Puma Biotechnology, Inc., a company dedicated to in-licensing and developing drugs for the treatment of cancer. Previously, Mr. Auerbach founded Cougar Biotechnology “Cougar”, a biotechnology company, in May 2003 and served as the company’s Chief Executive Officer, President and as a member of its Board of Directors until July 2009. From July 2009 until January 2010 Mr. Auerbach served as the Co-Chairman of the Integration Steering Committee at Cougar after its acquisition by Johnson & Johnson. Mr. Auerbach received a B.S. in Biomedical Engineering from Boston University and an M.S. in Biomedical Engineering from the University of Southern California.
Troy E. Wilson

Troy E. Wilson自2013年10月18日以来担任董事。他自2012年11月以来是Avidity NanoMedicines LLC(私人生物制药公司)的总裁,首席执行官和管理委员会的成员,分别自2012年7月和2012年5月以来担任Wellspring Biosciences LLC(私人生物制药公司)的总裁和首席执行官,以及管理委员会成员。他分别从2007年4月到2012年1月和2007年8月到2012年1月担任Intellikine(私人生物制药公司)的总裁和首席执行官,以及董事会成员。他自2012年5月以来是Araxes Pharma LLC(私人生物制药公司)管理委员会成员。他拥有纽约大学(New York University)的法学博士学位,毕业于加州大学伯克利分校(University of California, Berkeley),获得有机化学博士学位和生物物理学学士学位。他被提名担任董事(因为他在金融和会计的背景以及他在生命科学行业的经验)。


Troy E. Wilson has been a director since October 2013. Dr. Wilson has been the President and Chief Executive Officer and a member of the board of directors of Kura Oncology, Inc., a public reporting clinical stage biopharmaceutical company discovering and developing personalized therapeutics for the treatment of solid tumors and blood cancers, since August 2014. He has also been the President and Chief Executive Officer and a member of the board of managers of Avidity NanoMedicines LLC, a private biopharmaceutical company, since November 2012 and the President and Chief Executive Officer and a member of the board of managers of Wellspring Biosciences LLC, a private biopharmaceutical company, since July 2012 and May 2012 respectively. He has served as a director of Zosano Pharma Corporation, a public clinical stage specialty pharmaceutical company that has developed a proprietary transdermal microneedle patch system to deliver its proprietary formulations of existing drugs through the skin for the treatment of a variety of indications, since June 2014 and as a member of the board of managers of Araxes Pharma LLC, a private biopharmaceutical company, since May 2012. Dr. Wilson served as the President and Chief Executive Officer and a member of the board of directors of Intellikine, a private biopharmaceutical company, from April 2007 to January 2012 and from August 2007 to January 2012 respectively. He holds a J.D. from New York University and graduated with a Ph.D. in bioorganic chemistry and a B.A. in biophysics from the University of California, Berkeley.
Troy E. Wilson自2013年10月18日以来担任董事。他自2012年11月以来是Avidity NanoMedicines LLC(私人生物制药公司)的总裁,首席执行官和管理委员会的成员,分别自2012年7月和2012年5月以来担任Wellspring Biosciences LLC(私人生物制药公司)的总裁和首席执行官,以及管理委员会成员。他分别从2007年4月到2012年1月和2007年8月到2012年1月担任Intellikine(私人生物制药公司)的总裁和首席执行官,以及董事会成员。他自2012年5月以来是Araxes Pharma LLC(私人生物制药公司)管理委员会成员。他拥有纽约大学(New York University)的法学博士学位,毕业于加州大学伯克利分校(University of California, Berkeley),获得有机化学博士学位和生物物理学学士学位。他被提名担任董事(因为他在金融和会计的背景以及他在生命科学行业的经验)。
Troy E. Wilson has been a director since October 2013. Dr. Wilson has been the President and Chief Executive Officer and a member of the board of directors of Kura Oncology, Inc., a public reporting clinical stage biopharmaceutical company discovering and developing personalized therapeutics for the treatment of solid tumors and blood cancers, since August 2014. He has also been the President and Chief Executive Officer and a member of the board of managers of Avidity NanoMedicines LLC, a private biopharmaceutical company, since November 2012 and the President and Chief Executive Officer and a member of the board of managers of Wellspring Biosciences LLC, a private biopharmaceutical company, since July 2012 and May 2012 respectively. He has served as a director of Zosano Pharma Corporation, a public clinical stage specialty pharmaceutical company that has developed a proprietary transdermal microneedle patch system to deliver its proprietary formulations of existing drugs through the skin for the treatment of a variety of indications, since June 2014 and as a member of the board of managers of Araxes Pharma LLC, a private biopharmaceutical company, since May 2012. Dr. Wilson served as the President and Chief Executive Officer and a member of the board of directors of Intellikine, a private biopharmaceutical company, from April 2007 to January 2012 and from August 2007 to January 2012 respectively. He holds a J.D. from New York University and graduated with a Ph.D. in bioorganic chemistry and a B.A. in biophysics from the University of California, Berkeley.

高管简历

中英对照 |  中文 |  英文
Robert Charnas

Robert Charnas自2016年5月起担任监管事务和项目管理高级副总裁。2013年2月至2016年5月,他曾担任Janssen R&D的复合开发团队负责人,在那里他曾领导Zytiga公司的前列腺癌持续开发。2008年4月至2013年2月,他在Cougar Biotechnology通过北美、欧洲和亚洲的3期开发计划和批准,担任醋酸阿比特龙治疗晚期前列腺癌的全球监管领导人,直到2009年7月被强生公司收购。Charnas从2003年7月到2008年4月担任Amgen Neupogen Filgrastim,Neulasta(PEG-Filgrastim)和Xgeva(denosumab)全球监管主管。从2001年到2003年,他曾担任the Antiviral Famciclovir公司的临床领导,以及Novartis公司的Lumiracoxib公司的临床项目经理。加入Novartis公司之前,他曾任职Hoffmann-La Roche公司的传染病领域,在那里他曾担任研究实验室和医疗事务职务,Charnas博士在密歇根大学(University of Michigan)获得学士学位,在哈佛大学(Harvard University)获得化学博士学位,然后在法国斯特拉斯堡Louis Pasteur大学和哈佛医学院接受博士后培训。他是the American Society of Clinical Oncology和the Regulatory Affairs Professionals Society的成员。


Robert Charnas has served as our Senior Vice President of Regulatory Affairs and Project Management since May 2016. Dr. Charnas was a Compound Development Team Leader at Janssen R&D from February 2013 to May 2016 where he led the continuing development of Zytiga in prostate cancer. He served as Global Regulatory Leader for abiraterone acetate in the treatment of advanced prostate cancer through the Phase 3 development program and approvals in North America, Europe and Asia from April 2008 to February 2013 at Cougar Biotechnology until it was acquired by Johnson & Johnson in July 2009. From July 2003 to April 2008 Dr. Charnas served as global regulatory leader at Amgen for Neupogen filgrastim, Neulasta (peg-filgrastim), and Xgeva (denosumab). From 2001 to 2003 he served as clinical leader for the antiviral famciclovir and as clinical project manager for lumiracoxib at Novartis. Prior to joining Novartis, he worked in the field of infectious diseases at Hoffmann-La Roche, where he held positions in the research laboratory and medical affairs, finishing as Regulatory leader for the development of peg-interferon alfa-2a in the treatment of Hepatitis C. Dr. Charnas received a B.S from the University of Michigan and a Ph.D. in Chemistry at Harvard University before post-doctoral training at the Université Louis Pasteur in Strasbourg, France and Harvard Medical School. He is a member of the American Society of Clinical Oncology and the Regulatory Affairs Professionals Society.
Robert Charnas自2016年5月起担任监管事务和项目管理高级副总裁。2013年2月至2016年5月,他曾担任Janssen R&D的复合开发团队负责人,在那里他曾领导Zytiga公司的前列腺癌持续开发。2008年4月至2013年2月,他在Cougar Biotechnology通过北美、欧洲和亚洲的3期开发计划和批准,担任醋酸阿比特龙治疗晚期前列腺癌的全球监管领导人,直到2009年7月被强生公司收购。Charnas从2003年7月到2008年4月担任Amgen Neupogen Filgrastim,Neulasta(PEG-Filgrastim)和Xgeva(denosumab)全球监管主管。从2001年到2003年,他曾担任the Antiviral Famciclovir公司的临床领导,以及Novartis公司的Lumiracoxib公司的临床项目经理。加入Novartis公司之前,他曾任职Hoffmann-La Roche公司的传染病领域,在那里他曾担任研究实验室和医疗事务职务,Charnas博士在密歇根大学(University of Michigan)获得学士学位,在哈佛大学(Harvard University)获得化学博士学位,然后在法国斯特拉斯堡Louis Pasteur大学和哈佛医学院接受博士后培训。他是the American Society of Clinical Oncology和the Regulatory Affairs Professionals Society的成员。
Robert Charnas has served as our Senior Vice President of Regulatory Affairs and Project Management since May 2016. Dr. Charnas was a Compound Development Team Leader at Janssen R&D from February 2013 to May 2016 where he led the continuing development of Zytiga in prostate cancer. He served as Global Regulatory Leader for abiraterone acetate in the treatment of advanced prostate cancer through the Phase 3 development program and approvals in North America, Europe and Asia from April 2008 to February 2013 at Cougar Biotechnology until it was acquired by Johnson & Johnson in July 2009. From July 2003 to April 2008 Dr. Charnas served as global regulatory leader at Amgen for Neupogen filgrastim, Neulasta (peg-filgrastim), and Xgeva (denosumab). From 2001 to 2003 he served as clinical leader for the antiviral famciclovir and as clinical project manager for lumiracoxib at Novartis. Prior to joining Novartis, he worked in the field of infectious diseases at Hoffmann-La Roche, where he held positions in the research laboratory and medical affairs, finishing as Regulatory leader for the development of peg-interferon alfa-2a in the treatment of Hepatitis C. Dr. Charnas received a B.S from the University of Michigan and a Ph.D. in Chemistry at Harvard University before post-doctoral training at the Université Louis Pasteur in Strasbourg, France and Harvard Medical School. He is a member of the American Society of Clinical Oncology and the Regulatory Affairs Professionals Society.
Steven Lo

Steven Lo,2010年9月他加入公司担任商业运营副总裁,2013年11月晋升为高级副总裁兼首席商务官。他在制药和生物技术行业拥有超过19年的商业经验。从1997至2010年他在Genentech公司(一家生物技术公司)担任营销,销售和市场管理的职位,该公司在2009年3月成为罗氏集团的成员,担任特许经营主管的职位,领导该公司的内分泌学市场营销和销售组织。他收到了美国加州大学戴维斯分校的理学士学位和南加州大学的卫生管理硕士学位。


Steven Lo has served as our President and Chief Executive Officer and as a member of our Board of Directors since October 2019. Previously, from September 2015 to October 2019 Mr. Lo served as Chief Commercial Officer of Puma Biotechnology, Inc., a publicly-held biopharmaceutical company. Prior to joining Puma, Mr. Lo held a number of positions at Corcept Therapeutics Incorporated, a publicly-held pharmaceutical company, from September 2010 to September 2015 including Senior Vice President, Oncology, Senior Vice President & Chief Commercial Officer and Vice President & Head of Commercial Operations. Prior to Corcept, Mr. Lo was with Genentech, Inc. from December 1997 to September 2010. At Genentech, Mr. Lo held a number of positions, including Senior Director, Oncology Marketing, where he prepared and led the first U.S. launch of Herceptin® in adjuvant HER2-positive breast cancer. His other leadership roles at Genentech included Franchise Head, Endocrinology and Senior Director of Managed Care. Mr. Lo received a B.S. in Microbiology from the University of California, Davis and a Master of Health Administration from the University of Southern California.
Steven Lo,2010年9月他加入公司担任商业运营副总裁,2013年11月晋升为高级副总裁兼首席商务官。他在制药和生物技术行业拥有超过19年的商业经验。从1997至2010年他在Genentech公司(一家生物技术公司)担任营销,销售和市场管理的职位,该公司在2009年3月成为罗氏集团的成员,担任特许经营主管的职位,领导该公司的内分泌学市场营销和销售组织。他收到了美国加州大学戴维斯分校的理学士学位和南加州大学的卫生管理硕士学位。
Steven Lo has served as our President and Chief Executive Officer and as a member of our Board of Directors since October 2019. Previously, from September 2015 to October 2019 Mr. Lo served as Chief Commercial Officer of Puma Biotechnology, Inc., a publicly-held biopharmaceutical company. Prior to joining Puma, Mr. Lo held a number of positions at Corcept Therapeutics Incorporated, a publicly-held pharmaceutical company, from September 2010 to September 2015 including Senior Vice President, Oncology, Senior Vice President & Chief Commercial Officer and Vice President & Head of Commercial Operations. Prior to Corcept, Mr. Lo was with Genentech, Inc. from December 1997 to September 2010. At Genentech, Mr. Lo held a number of positions, including Senior Director, Oncology Marketing, where he prepared and led the first U.S. launch of Herceptin® in adjuvant HER2-positive breast cancer. His other leadership roles at Genentech included Franchise Head, Endocrinology and Senior Director of Managed Care. Mr. Lo received a B.S. in Microbiology from the University of California, Davis and a Master of Health Administration from the University of Southern California.
Charles R. Eyler

Charles R. Eyler。于2011年10月4日担任我们的财务和行政管理的高级副总裁和财务总监。在2011年10月4日前,他于2011年9月1日Puma创立之初就担任这些职务。在加入Puma之前,Mr. Eyler在Cougar担任财务高级副总裁,直到2009年7月Cougar被Johnson & Johnson收购。2006年4月至2009年7月,他担任Cougar的财务总监。2009年7月至2010年3月,Mr. Eyler在Cougar(作为Johnson & Johnson的一部分)整合指导委员会任职,监管Cougar的财务和信息技术功能和Johnson & Johnson的整合。2010年4月至2011年9月,Mr. Eyler尝试了许多创业机会。在加入Cougar之前,1999年3月至2004年1月。Mr. Eyler担任Hayes Medical Inc.的首席财务官和首席运营官。Mr. Eyler在Drexel University获得学士学位,在Saint Francis College获得工商管理硕士学位。


Charles R. Eyler has served as our Senior Vice President, Finance and Administration and Treasurer since October 2011. Prior to October 2011 he served in such capacity at Puma beginning in September 2011. Prior to joining Puma, Mr. Eyler served as Senior Vice President of Finance at Cougar until July 2009 when Cougar was acquired by Johnson & Johnson. He also served as Treasurer of Cougar from April 2006 to July 2009. From July 2009 until March 2010 Mr. Eyler served on the Integration Steering Committee at Cougar as part of Johnson & Johnson and oversaw the integration of Cougar’s finance and IT functions with those of Johnson & Johnson. From April 2010 until September 2011 Mr. Eyler explored various entrepreneurial and other opportunities. Prior to joining Cougar, Mr. Eyler served as Chief Financial Officer and Chief Operating Officer of Hayes Medical Inc. from March 1999 to January 2004. Mr. Eyler received his B.S. from Drexel University and his M.B.A. from Saint Francis College.
Charles R. Eyler。于2011年10月4日担任我们的财务和行政管理的高级副总裁和财务总监。在2011年10月4日前,他于2011年9月1日Puma创立之初就担任这些职务。在加入Puma之前,Mr. Eyler在Cougar担任财务高级副总裁,直到2009年7月Cougar被Johnson & Johnson收购。2006年4月至2009年7月,他担任Cougar的财务总监。2009年7月至2010年3月,Mr. Eyler在Cougar(作为Johnson & Johnson的一部分)整合指导委员会任职,监管Cougar的财务和信息技术功能和Johnson & Johnson的整合。2010年4月至2011年9月,Mr. Eyler尝试了许多创业机会。在加入Cougar之前,1999年3月至2004年1月。Mr. Eyler担任Hayes Medical Inc.的首席财务官和首席运营官。Mr. Eyler在Drexel University获得学士学位,在Saint Francis College获得工商管理硕士学位。
Charles R. Eyler has served as our Senior Vice President, Finance and Administration and Treasurer since October 2011. Prior to October 2011 he served in such capacity at Puma beginning in September 2011. Prior to joining Puma, Mr. Eyler served as Senior Vice President of Finance at Cougar until July 2009 when Cougar was acquired by Johnson & Johnson. He also served as Treasurer of Cougar from April 2006 to July 2009. From July 2009 until March 2010 Mr. Eyler served on the Integration Steering Committee at Cougar as part of Johnson & Johnson and oversaw the integration of Cougar’s finance and IT functions with those of Johnson & Johnson. From April 2010 until September 2011 Mr. Eyler explored various entrepreneurial and other opportunities. Prior to joining Cougar, Mr. Eyler served as Chief Financial Officer and Chief Operating Officer of Hayes Medical Inc. from March 1999 to January 2004. Mr. Eyler received his B.S. from Drexel University and his M.B.A. from Saint Francis College.
Richard P. Bryce

Richard P. Bryce是医学学士,皇家全科医学院院士。Dr. Bryce于2012年6月20日担任我们临床研究和开发的高级副总裁。2008年9月至2012年6月,Dr. Bryce在Onyx Pharmaceuticals(一家生物制药公司)担任高级医学指导,他监管多发性骨髓瘤治疗实验的三期临床实验项目和用于治疗乳腺癌和结直肠癌的索拉非尼的二期临床试验项目。2007年8月至2008年8月, Dr. Bryce ICON Clinical Research(一个临床研究组织)的高级医学指导,他负责在肿瘤药物临床试验中开发和评估肿瘤协议,医学监控和监管药物安全活动。2005年5月至2007年7月,他担任Ergomed Clinical Research(一个临床研究组织)医学事务的执行副总裁, 他努力建立美国业务,负责全球一期单元活动,药物安全,医学写作和管理事务,并监管公司在许多肿瘤生物科技公司的咨询服务的前景。2003年4月至2005年5月,Dr. Bryce 在Roche担任国际医学领导者,他监管乳腺癌希罗达治疗方案的全球四期临床实验项目。Dr. Bryce在苏格兰University of Edinburgh获得医学科学学士学位和主要医学学位(MBChB);他在伦敦Royal College of Obstetricians and Gynaecologists妇产科获得研究生证书;在Royal College of Physicians of the United Kingdom。获得儿童健康和药物医学获得研究生证书。他是英国全科医师皇家学院和皇家医师学院(医药学院)(Royal College of General Practitioners and the Royal College of Physicians (Faculty of Pharmaceutical Medicine) of the United Kingdom。)的成员。他也是美国临床肿瘤协会,美国血液协会和欧洲肿瘤内科协会(American Society of Clinical Oncology, the American Society of Hematology and the European Society of Medical Oncology)。的成员。


Richard P. Bryce has served as our Senior Vice President, Clinical Research and Development since June 2012. Dr. Bryce previously served as Senior Medical Director for Onyx Pharmaceuticals, a biopharmaceutical company, from September 2008 to June 2012 where he oversaw the Phase III clinical trial program of carfilzomib for the treatment of multiple myeloma and the Phase II clinical trial program of sorafenib for the treatment of breast and colorectal cancers. From August 2007 to August 2008 Dr. Bryce served as Senior Medical Director for ICON Clinical Research, a clinical research organization, where he was responsible for developing and evaluating oncology protocols, medical monitoring, and overseeing drug safety management activities in connection with the clinical trials of oncology drugs. From May 2005 until July 2007 he served as Executive Vice President of Medical Affairs at Ergomed Clinical Research, a clinical research organization, where he worked to establish the company’s U.S. operations, had overall responsibility for the global Phase I unit activities, drug safety, medical writing and regulatory affairs, and oversaw the company’s provision of consulting services to various oncology-focused biotechnology companies. From April 2003 to May 2005 Dr. Bryce served as International Medical Leader at Roche, where he oversaw the global Phase IV clinical trial program of Xeloda® capecitabine for the treatment of breast cancer. Dr. Bryce holds a BSc in Medical Sciences and his primary medical degree (MBChB) from the University of Edinburgh, Scotland. He also holds post-graduate diplomas in Obstetrics and Gynaecology from the Royal College of Obstetricians and Gynaecologists of London and in Child Health and Pharmaceutical Medicine from the Royal College of Physicians of the United Kingdom. He is a member of the Royal College of General Practitioners and the Royal College of Physicians (Faculty of Pharmaceutical Medicine) of the United Kingdom. He is also a member of the American Society of Clinical Oncology, the American Society of Hematology and the European Society of Medical Oncology.
Richard P. Bryce是医学学士,皇家全科医学院院士。Dr. Bryce于2012年6月20日担任我们临床研究和开发的高级副总裁。2008年9月至2012年6月,Dr. Bryce在Onyx Pharmaceuticals(一家生物制药公司)担任高级医学指导,他监管多发性骨髓瘤治疗实验的三期临床实验项目和用于治疗乳腺癌和结直肠癌的索拉非尼的二期临床试验项目。2007年8月至2008年8月, Dr. Bryce ICON Clinical Research(一个临床研究组织)的高级医学指导,他负责在肿瘤药物临床试验中开发和评估肿瘤协议,医学监控和监管药物安全活动。2005年5月至2007年7月,他担任Ergomed Clinical Research(一个临床研究组织)医学事务的执行副总裁, 他努力建立美国业务,负责全球一期单元活动,药物安全,医学写作和管理事务,并监管公司在许多肿瘤生物科技公司的咨询服务的前景。2003年4月至2005年5月,Dr. Bryce 在Roche担任国际医学领导者,他监管乳腺癌希罗达治疗方案的全球四期临床实验项目。Dr. Bryce在苏格兰University of Edinburgh获得医学科学学士学位和主要医学学位(MBChB);他在伦敦Royal College of Obstetricians and Gynaecologists妇产科获得研究生证书;在Royal College of Physicians of the United Kingdom。获得儿童健康和药物医学获得研究生证书。他是英国全科医师皇家学院和皇家医师学院(医药学院)(Royal College of General Practitioners and the Royal College of Physicians (Faculty of Pharmaceutical Medicine) of the United Kingdom。)的成员。他也是美国临床肿瘤协会,美国血液协会和欧洲肿瘤内科协会(American Society of Clinical Oncology, the American Society of Hematology and the European Society of Medical Oncology)。的成员。
Richard P. Bryce has served as our Senior Vice President, Clinical Research and Development since June 2012. Dr. Bryce previously served as Senior Medical Director for Onyx Pharmaceuticals, a biopharmaceutical company, from September 2008 to June 2012 where he oversaw the Phase III clinical trial program of carfilzomib for the treatment of multiple myeloma and the Phase II clinical trial program of sorafenib for the treatment of breast and colorectal cancers. From August 2007 to August 2008 Dr. Bryce served as Senior Medical Director for ICON Clinical Research, a clinical research organization, where he was responsible for developing and evaluating oncology protocols, medical monitoring, and overseeing drug safety management activities in connection with the clinical trials of oncology drugs. From May 2005 until July 2007 he served as Executive Vice President of Medical Affairs at Ergomed Clinical Research, a clinical research organization, where he worked to establish the company’s U.S. operations, had overall responsibility for the global Phase I unit activities, drug safety, medical writing and regulatory affairs, and oversaw the company’s provision of consulting services to various oncology-focused biotechnology companies. From April 2003 to May 2005 Dr. Bryce served as International Medical Leader at Roche, where he oversaw the global Phase IV clinical trial program of Xeloda® capecitabine for the treatment of breast cancer. Dr. Bryce holds a BSc in Medical Sciences and his primary medical degree (MBChB) from the University of Edinburgh, Scotland. He also holds post-graduate diplomas in Obstetrics and Gynaecology from the Royal College of Obstetricians and Gynaecologists of London and in Child Health and Pharmaceutical Medicine from the Royal College of Physicians of the United Kingdom. He is a member of the Royal College of General Practitioners and the Royal College of Physicians (Faculty of Pharmaceutical Medicine) of the United Kingdom. He is also a member of the American Society of Clinical Oncology, the American Society of Hematology and the European Society of Medical Oncology.
Alan H. Auerbach

Alan H. Auerbach,2011年5月起,他担任我公司董事会成员,2010年10月至合并,担任Former Operating Company董事会成员。他目前是彪马生物技术公司(Puma Biotechnology, Inc.)的创始人、首席执行官、总裁和董事会主席, 该公司成立于2010年,开发治疗癌症的药物并获得进口许可。2003年5月,他成立Cougar Biotechnology,担任首席执行官、总裁和董事会成员直到2009年7月;2009年7月至2010年1月,担任强生旗下Cougar集成指导委员会共同主席。他在波士顿大学(Boston University)获得生物医学工程学士学位,在南加利福尼亚大学(University of Southern California)获得生物医学工程硕士学位。


Alan H. Auerbach has served on our Board since May 2011 and served as a member of the Board of Directors of our predecessor company from October 2010 until May 2011. Mr. Auerbach is currently the Founder, Chief Executive Officer, President and Chairman of the Board of Directors of Puma Biotechnology, Inc., a company dedicated to in-licensing and developing drugs for the treatment of cancer. Previously, Mr. Auerbach founded Cougar Biotechnology “Cougar”, a biotechnology company, in May 2003 and served as the company’s Chief Executive Officer, President and as a member of its Board of Directors until July 2009. From July 2009 until January 2010 Mr. Auerbach served as the Co-Chairman of the Integration Steering Committee at Cougar after its acquisition by Johnson & Johnson. Mr. Auerbach received a B.S. in Biomedical Engineering from Boston University and an M.S. in Biomedical Engineering from the University of Southern California.
Alan H. Auerbach,2011年5月起,他担任我公司董事会成员,2010年10月至合并,担任Former Operating Company董事会成员。他目前是彪马生物技术公司(Puma Biotechnology, Inc.)的创始人、首席执行官、总裁和董事会主席, 该公司成立于2010年,开发治疗癌症的药物并获得进口许可。2003年5月,他成立Cougar Biotechnology,担任首席执行官、总裁和董事会成员直到2009年7月;2009年7月至2010年1月,担任强生旗下Cougar集成指导委员会共同主席。他在波士顿大学(Boston University)获得生物医学工程学士学位,在南加利福尼亚大学(University of Southern California)获得生物医学工程硕士学位。
Alan H. Auerbach has served on our Board since May 2011 and served as a member of the Board of Directors of our predecessor company from October 2010 until May 2011. Mr. Auerbach is currently the Founder, Chief Executive Officer, President and Chairman of the Board of Directors of Puma Biotechnology, Inc., a company dedicated to in-licensing and developing drugs for the treatment of cancer. Previously, Mr. Auerbach founded Cougar Biotechnology “Cougar”, a biotechnology company, in May 2003 and served as the company’s Chief Executive Officer, President and as a member of its Board of Directors until July 2009. From July 2009 until January 2010 Mr. Auerbach served as the Co-Chairman of the Integration Steering Committee at Cougar after its acquisition by Johnson & Johnson. Mr. Auerbach received a B.S. in Biomedical Engineering from Boston University and an M.S. in Biomedical Engineering from the University of Southern California.