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
Eric E. Poma Chief Executive Officer and Chief Scientific Officer, Director 52 85.78万美元 未持股 2024-08-13
Gabriela Gruia Interim Chief Medical Officer and Director 68 19.05万美元 未持股 2024-08-13
Corsee Sanders Director 67 4.93万美元 未持股 2024-08-13
David R. Hoffmann Director 79 5.93万美元 未持股 2024-08-13
Harold E. Selick Chairman of the Board 69 8.73万美元 未持股 2024-08-13

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
Eric E. Poma Chief Executive Officer and Chief Scientific Officer, Director 52 85.78万美元 未持股 2024-08-13
Jason S. Kim President and Chief Financial Officer 49 57.92万美元 未持股 2024-08-13
Gabriela Gruia Interim Chief Medical Officer and Director 68 19.05万美元 未持股 2024-08-13

董事简历

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Eric E. Poma

Eric E. Poma,自2017年8月合并起担任本公司董事。Poma博士是公司的首席执行官兼首席科学官,并于2009年2月创立了Private Molecular,自成立以来一直在其董事会任职。从2005年3月到2008年9月,Poma博士担任Innovive Pharmaceuticals的业务发展副总裁,该公司被一家生物技术公司Innovive Pharmaceuticals收购。从2001年到2005年,他担任ImClone Systems,Inc.(现为副总裁0)的业务发展副副总裁,该公司是一家专注于抗体治疗的生物技术公司。作为Private Molecular的创始人并担任首席科学官,他领导了公司平台技术基础技术的发明,以及构成公司当前主要和临床前管道候选者的全部内容。Poma博士获得了博士学位。在微生物学和免疫学和学士学位在北卡罗来纳大学教堂山分校获得生物学博士学位,在纽约大学获得工商管理硕士学位。Molecular Templates, Inc.董事会得出结论认为,波马博士应担任公司董事,这是基于波马博士直接参与了Molecular Templates公司技术平台的创建和知识以及在该行业的丰富经验,这为Molecular Templates提供了宝贵的洞察力,Inc.董事会讨论涉及公司及其未来目标的事项。


Eric E. Poma,has been a director of the Company since August 2017, effective as of the Merger. Dr. Poma is the Chief Executive Officer and Chief Scientific Officer of the Company and founded Private Molecular in February 2009, serving on its board of directors since its inception. From March 2005 until September 2008, Dr. Poma was Vice President of Business Development of Innovive Pharmaceuticals, Inc. (acquired by Cytrx Corporation), a biotechnoloy company. As the founder of Private Molecular and in his role as Chief Scientific Officer, he led the invention of technology underlying the Company's platform technology and what constitutes the whole of the Company's current pipeline of candidates. Dr. Poma received his Ph.D. in Microbiology and Immunology and B.S. in Biology from the University of North Carolina at Chapel Hill and his M.B.A. from New York University.
Eric E. Poma,自2017年8月合并起担任本公司董事。Poma博士是公司的首席执行官兼首席科学官,并于2009年2月创立了Private Molecular,自成立以来一直在其董事会任职。从2005年3月到2008年9月,Poma博士担任Innovive Pharmaceuticals的业务发展副总裁,该公司被一家生物技术公司Innovive Pharmaceuticals收购。从2001年到2005年,他担任ImClone Systems,Inc.(现为副总裁0)的业务发展副副总裁,该公司是一家专注于抗体治疗的生物技术公司。作为Private Molecular的创始人并担任首席科学官,他领导了公司平台技术基础技术的发明,以及构成公司当前主要和临床前管道候选者的全部内容。Poma博士获得了博士学位。在微生物学和免疫学和学士学位在北卡罗来纳大学教堂山分校获得生物学博士学位,在纽约大学获得工商管理硕士学位。Molecular Templates, Inc.董事会得出结论认为,波马博士应担任公司董事,这是基于波马博士直接参与了Molecular Templates公司技术平台的创建和知识以及在该行业的丰富经验,这为Molecular Templates提供了宝贵的洞察力,Inc.董事会讨论涉及公司及其未来目标的事项。
Eric E. Poma,has been a director of the Company since August 2017, effective as of the Merger. Dr. Poma is the Chief Executive Officer and Chief Scientific Officer of the Company and founded Private Molecular in February 2009, serving on its board of directors since its inception. From March 2005 until September 2008, Dr. Poma was Vice President of Business Development of Innovive Pharmaceuticals, Inc. (acquired by Cytrx Corporation), a biotechnoloy company. As the founder of Private Molecular and in his role as Chief Scientific Officer, he led the invention of technology underlying the Company's platform technology and what constitutes the whole of the Company's current pipeline of candidates. Dr. Poma received his Ph.D. in Microbiology and Immunology and B.S. in Biology from the University of North Carolina at Chapel Hill and his M.B.A. from New York University.
Gabriela Gruia

Gabriela Gruia,自2023年5月起担任Aprea Therapeutics公司董事会成员。Gruia博士是一位肿瘤学家,在肿瘤药物开发领域拥有超过25年的经验,涵盖细胞和基因治疗、双特异性、生物制剂、免疫治疗和小分子领域,目前担任Gabriela Gruia咨询有限公司的创始人和负责人。从2020年2月到2021年1月,Gruia博士在Ichnos Sciences担任首席开发官,负责多个关键职能的开发活动,包括临床开发和临床运营、监管科学、临床药理学、毒理学和生物统计学。2004年8月至2020年2月,Gruia博士担任诺华肿瘤学高级副总裁兼全球监管事务主管,领导世界级的肿瘤监管事务组织,并与研究合作者、临床前开发、开发组织和高级管理层密切合作,监督所有监管活动。在诺华期间,Gruia博士领导了多个新分子实体的全球提交和批准,包括Tasigna 、Jakavi 、Afinitor 、Signifor 、Zykadia 、Farydak 、Rydapt 、Odomzo 、Kisqali 、Kymriah 、Adakveo 和Piqray 。Gruia博士是TSCAN Therapeutics、Tessa Therapeutics Ltd.和Molecular Templates, Inc.的董事会成员。Gruia博士在罗马尼亚布加勒斯特医学院获得医学博士学位,在法国巴黎的Rene Huguenin/Curie Institute癌症中心获得乳腺病理学和乳腺摄影硕士学位。她在法国巴黎勒内·笛卡尔大学完成了肿瘤学和血液学的培训。


Gabriela Gruia,has served as a member of board of directors since May 2021. Dr. Gruia founded Gabriela Gruia Consulting, LLC in January 2021. Prior to that, Dr. Gruia served as the Chief Development Officer at Ichnos Sciences Inc. from February 2020 to January 2021, where she oversaw several key functions including Regulatory Sciences, Clinical Operations, Clinical Pharmacology, Biostatistics and Drug Safety. Prior to her time at Ichnos Sciences Inc., Dr. Gruia served as Senior Vice President and Head of Regulatory Affairs for Novartis Oncology from February 2008 through February 2020, where she was responsible for leading the oncology regulatory affairs organization. Dr. Gruia has served on the boards of directors for Aprea Therapeutics, Inc. since 2023, Netris Pharma since 2023, and Molecular Templates, Inc. from March 2022 until its dissolution in December 2024. Dr. Gruia received her doctorate in medicine from Bucharest Medical School in Romania and has a Masters in Breast Pathology and Mammography from Rene Huguenin/Curie Institute Cancer Center in Paris, France. She received her training in oncology and hematology from Rene Descartes University in Paris, France.
Gabriela Gruia,自2023年5月起担任Aprea Therapeutics公司董事会成员。Gruia博士是一位肿瘤学家,在肿瘤药物开发领域拥有超过25年的经验,涵盖细胞和基因治疗、双特异性、生物制剂、免疫治疗和小分子领域,目前担任Gabriela Gruia咨询有限公司的创始人和负责人。从2020年2月到2021年1月,Gruia博士在Ichnos Sciences担任首席开发官,负责多个关键职能的开发活动,包括临床开发和临床运营、监管科学、临床药理学、毒理学和生物统计学。2004年8月至2020年2月,Gruia博士担任诺华肿瘤学高级副总裁兼全球监管事务主管,领导世界级的肿瘤监管事务组织,并与研究合作者、临床前开发、开发组织和高级管理层密切合作,监督所有监管活动。在诺华期间,Gruia博士领导了多个新分子实体的全球提交和批准,包括Tasigna 、Jakavi 、Afinitor 、Signifor 、Zykadia 、Farydak 、Rydapt 、Odomzo 、Kisqali 、Kymriah 、Adakveo 和Piqray 。Gruia博士是TSCAN Therapeutics、Tessa Therapeutics Ltd.和Molecular Templates, Inc.的董事会成员。Gruia博士在罗马尼亚布加勒斯特医学院获得医学博士学位,在法国巴黎的Rene Huguenin/Curie Institute癌症中心获得乳腺病理学和乳腺摄影硕士学位。她在法国巴黎勒内·笛卡尔大学完成了肿瘤学和血液学的培训。
Gabriela Gruia,has served as a member of board of directors since May 2021. Dr. Gruia founded Gabriela Gruia Consulting, LLC in January 2021. Prior to that, Dr. Gruia served as the Chief Development Officer at Ichnos Sciences Inc. from February 2020 to January 2021, where she oversaw several key functions including Regulatory Sciences, Clinical Operations, Clinical Pharmacology, Biostatistics and Drug Safety. Prior to her time at Ichnos Sciences Inc., Dr. Gruia served as Senior Vice President and Head of Regulatory Affairs for Novartis Oncology from February 2008 through February 2020, where she was responsible for leading the oncology regulatory affairs organization. Dr. Gruia has served on the boards of directors for Aprea Therapeutics, Inc. since 2023, Netris Pharma since 2023, and Molecular Templates, Inc. from March 2022 until its dissolution in December 2024. Dr. Gruia received her doctorate in medicine from Bucharest Medical School in Romania and has a Masters in Breast Pathology and Mammography from Rene Huguenin/Curie Institute Cancer Center in Paris, France. She received her training in oncology and hematology from Rene Descartes University in Paris, France.
Corsee Sanders

Corsee Sanders,自2019年12月起担任公司董事。从2019年11月到2020年2月,桑德斯博士担任百时美施贵宝全球发展集团的战略顾问。此前,桑德斯博士自2018年3月至2019年11月担任Celgene首席医疗官办公室的战略顾问,确保将Juno Therapeutics的开发组织有效整合到Celgene组织中,特别是独特的CAR T方面,为支持标签的CAR T遗留Juno项目(JCAR017 )提供建议,并就临床开发组织的发展向首席医疗官和首席医疗官领导团队提供建议。2017年1月至2018年3月,桑德斯博士担任Juno Therapeutics执行委员会成员,担任战略和发展业务主管,负责战略业务、定量科学、生物样本和临床业务。桑德斯博士曾于2011年至2017年担任基因泰克/罗氏晚期临床项目委员会成员,并于2012年至2017年担任基因泰克/罗氏晚期临床业务全球主管,负责领导近2500名员工在70多个国家规划和开展全球开发和本土临床试验,这些员工分布在5个战略地点和20个当地国家。桑德斯博士直接参与和/或监督了多种已获批准的医药产品的开发,包括Claritin 、Rituxan 、Herceptin 、TNKase 、Cathflo 、Xolair、Avastin 、Tarceva 、Lucentis 、Zelboraf 、Perjeta 、Erivedge 、Gazyva 、Kadcyla 、Alecensa 、Cotellic 、Venclexta 、Tecentriq 、Ocrevus 、Hemlibra ,以及用于NHL的CAR T细胞疗法JCAR017 。她目前是Fred Hutchinson癌症研究中心董事会成员。桑德斯博士目前担任生物制药公司的董事,如Ultragenyx Pharmaceuticals,Inc.,百济神州有限公司,AltruBio Inc.和传奇生物技术公司。桑德斯博士获得了统计学学士和硕士学位,以优异成绩从菲律宾大学毕业,并在宾夕法尼亚大学沃顿商学院获得统计学硕士和博士学位。


Corsee Sanders,has been a director of the Company since December 2019. From November 2019 to February 2020, Dr. Sanders served as a Strategic Advisor to the Global Development Group of Bristol Myers Squibb. Previously, Dr. Sanders served as Strategic Advisor to the Office of the Celgene Chief Medical Officer, since March 2018 to November 2019, ensuring effective integration of Juno Therapeutics' Development Organization into the Celgene Organization, specifically the unique CAR T aspects, advising the label-enabling CAR T legacy Juno program (JCAR017), and advising the Chief Medical Officer and the Chief Medical Officer's leadership team in evolving the clinical development organization. From January 2017 to March 2018, Dr. Sanders was a Member of the Juno Therapeutics Executive Committee as Head of Strategic and Development Operations, with responsibilities for strategic operations, quantitative sciences, biosample and clinical operations. Dr. Sanders was a Member of the Genentech/Roche Late-Stage Portfolio Committee from 2011 to 2017, and Global Head of the Genentech/Roche Late Stage Clinical Operations from 2012 to 2017, with responsibility for leading nearly 2,500 employees, across 5 strategic and 20 local country sites, in planning and conducting global development and local clinical trials in over 70 countries. Dr. Sanders has directly contributed and/or provided oversight in developing multiple approved pharmaceutical products including Claritin, Rituxan, Herceptin, TNKase, Cathflo, Xolair, Avastin, Tarceva, Lucentis, Zelboraf, Perjeta, Erivedge, Gazyva, Kadcyla, Alecensa, Cotellic, Venclexta, Tecentriq, Ocrevus, Hemlibra, and JCAR017, a CAR T cell therapy for NHL. She currently serves as a member of the Board of Trustees for the Fred Hutchinson Cancer Research Center. Dr. Sanders currently serves as a director for biopharmaceutical companies, such as Ultragenyx Pharmaceuticals, Inc., Beigene, Ltd., AltruBio Inc. and Legend Biotech Corporation. Dr. Sanders earned her B.S. and M.S. in statistics, graduating Magna Cum Laude from the University of the Philippines, and her M.A. and Ph.D. in statistics from the Wharton Doctoral Program at the University of Pennsylvania.
Corsee Sanders,自2019年12月起担任公司董事。从2019年11月到2020年2月,桑德斯博士担任百时美施贵宝全球发展集团的战略顾问。此前,桑德斯博士自2018年3月至2019年11月担任Celgene首席医疗官办公室的战略顾问,确保将Juno Therapeutics的开发组织有效整合到Celgene组织中,特别是独特的CAR T方面,为支持标签的CAR T遗留Juno项目(JCAR017 )提供建议,并就临床开发组织的发展向首席医疗官和首席医疗官领导团队提供建议。2017年1月至2018年3月,桑德斯博士担任Juno Therapeutics执行委员会成员,担任战略和发展业务主管,负责战略业务、定量科学、生物样本和临床业务。桑德斯博士曾于2011年至2017年担任基因泰克/罗氏晚期临床项目委员会成员,并于2012年至2017年担任基因泰克/罗氏晚期临床业务全球主管,负责领导近2500名员工在70多个国家规划和开展全球开发和本土临床试验,这些员工分布在5个战略地点和20个当地国家。桑德斯博士直接参与和/或监督了多种已获批准的医药产品的开发,包括Claritin 、Rituxan 、Herceptin 、TNKase 、Cathflo 、Xolair、Avastin 、Tarceva 、Lucentis 、Zelboraf 、Perjeta 、Erivedge 、Gazyva 、Kadcyla 、Alecensa 、Cotellic 、Venclexta 、Tecentriq 、Ocrevus 、Hemlibra ,以及用于NHL的CAR T细胞疗法JCAR017 。她目前是Fred Hutchinson癌症研究中心董事会成员。桑德斯博士目前担任生物制药公司的董事,如Ultragenyx Pharmaceuticals,Inc.,百济神州有限公司,AltruBio Inc.和传奇生物技术公司。桑德斯博士获得了统计学学士和硕士学位,以优异成绩从菲律宾大学毕业,并在宾夕法尼亚大学沃顿商学院获得统计学硕士和博士学位。
Corsee Sanders,has been a director of the Company since December 2019. From November 2019 to February 2020, Dr. Sanders served as a Strategic Advisor to the Global Development Group of Bristol Myers Squibb. Previously, Dr. Sanders served as Strategic Advisor to the Office of the Celgene Chief Medical Officer, since March 2018 to November 2019, ensuring effective integration of Juno Therapeutics' Development Organization into the Celgene Organization, specifically the unique CAR T aspects, advising the label-enabling CAR T legacy Juno program (JCAR017), and advising the Chief Medical Officer and the Chief Medical Officer's leadership team in evolving the clinical development organization. From January 2017 to March 2018, Dr. Sanders was a Member of the Juno Therapeutics Executive Committee as Head of Strategic and Development Operations, with responsibilities for strategic operations, quantitative sciences, biosample and clinical operations. Dr. Sanders was a Member of the Genentech/Roche Late-Stage Portfolio Committee from 2011 to 2017, and Global Head of the Genentech/Roche Late Stage Clinical Operations from 2012 to 2017, with responsibility for leading nearly 2,500 employees, across 5 strategic and 20 local country sites, in planning and conducting global development and local clinical trials in over 70 countries. Dr. Sanders has directly contributed and/or provided oversight in developing multiple approved pharmaceutical products including Claritin, Rituxan, Herceptin, TNKase, Cathflo, Xolair, Avastin, Tarceva, Lucentis, Zelboraf, Perjeta, Erivedge, Gazyva, Kadcyla, Alecensa, Cotellic, Venclexta, Tecentriq, Ocrevus, Hemlibra, and JCAR017, a CAR T cell therapy for NHL. She currently serves as a member of the Board of Trustees for the Fred Hutchinson Cancer Research Center. Dr. Sanders currently serves as a director for biopharmaceutical companies, such as Ultragenyx Pharmaceuticals, Inc., Beigene, Ltd., AltruBio Inc. and Legend Biotech Corporation. Dr. Sanders earned her B.S. and M.S. in statistics, graduating Magna Cum Laude from the University of the Philippines, and her M.A. and Ph.D. in statistics from the Wharton Doctoral Program at the University of Pennsylvania.
David R. Hoffmann

David R. Hoffmann,2002年12月起担任董事,2010年12月起担任首席独立董事。他从ALZA Corporation(现Johnson & Johnson成员公司)退休,1992至2002年10月退休前担任副总裁和财务主管;1982至1992年担任财务副总裁;1976至1982年担任会计和财务主管。他现在是专注于游轮旅游、财务及福利咨询大型集团公司Hoffmann Associates的首席执行官。他获有the University of Colorado的工商管理学位。他现在是生物科技公司Threshold Pharmaceuticals的董事会成员和审计委员会主席。


David R. Hoffmann,has been a director of the Company since August 2017, effective as of the Merger, and served as a director of Pre-Merger Threshold since April 2007. Since 2002, Mr. Hoffmann has served as the Chief Executive Officer of Hoffmann Associates, a multi-group company specializing in cruise travel and financial and benefit consulting. Mr. Hoffmann holds a B.S. in Business Administration from the University of Colorado.
David R. Hoffmann,2002年12月起担任董事,2010年12月起担任首席独立董事。他从ALZA Corporation(现Johnson & Johnson成员公司)退休,1992至2002年10月退休前担任副总裁和财务主管;1982至1992年担任财务副总裁;1976至1982年担任会计和财务主管。他现在是专注于游轮旅游、财务及福利咨询大型集团公司Hoffmann Associates的首席执行官。他获有the University of Colorado的工商管理学位。他现在是生物科技公司Threshold Pharmaceuticals的董事会成员和审计委员会主席。
David R. Hoffmann,has been a director of the Company since August 2017, effective as of the Merger, and served as a director of Pre-Merger Threshold since April 2007. Since 2002, Mr. Hoffmann has served as the Chief Executive Officer of Hoffmann Associates, a multi-group company specializing in cruise travel and financial and benefit consulting. Mr. Hoffmann holds a B.S. in Business Administration from the University of Colorado.
Harold E. Selick

Harold E. Selick于2009年8月被选为董事。 Selick博士从2002年6月开始担任Threshold制药股份有限公司(Threshold Pharmaceuticals)的首席执行官兼董事,该公司是一家上市的生物技术公司。从2002年6月到2007年7月,Selick博士还是Sofinnova 风险股份有限公司(Sofinnova Ventures, Inc.)的风险合伙人,该公司是一家风险投资公司。从1999年1月到2002年4月,他担任Camitro股份有限公司( Camitro Corporation)的首席执行官,该公司是一家生物技术公司。从1992年到1999年,他在Affymax研究学院(Affymax Research Institute)任职,这是为葛兰素威康公司(Glaxo Wellcome plc)进行药物研发的技术开发中心,其最后担任的职务是研究部的副总裁。在Affymax任职前,Selick博士在蛋白质设计实验室股份有限公司(Protein Design Labs,现在称为PDL生物制药股份有限公司, PDL BioPharma, Inc.)和Anergen股份有限公司(Anergen, Inc)担任科研职位。作为蛋白质设计实验室股份有限公司的职业科学家,他与人合作发明了一种技术,该技术有潜力开发为完全无排异的抗体疗法,他将其应用于PDL公司的第一个产品——赛尼哌(达利珠单抗),罗氏公司(Roche)将该产品开发并商业化,并将其用于阻止肾移植排异反应。Selick博士担任催化剂生物科学与领导者疗法股份有限公司(Catalyst Biosciences and Protagonist Therapeutics)的董事会主席,该公司是一家私人所有的制药公司。Selick博士在宾夕法尼亚大学获得文学学士学位与博士学位,他还是旧金山加利福尼亚大学的达蒙拉尼恩-沃尔特温切尔癌症基金( Damon Runyon-Walter Winchell Cancer Fund)的研究员和美国癌症协会(American Cancer Society)的高级研究员。


Harold E. Selick,is chairperson of the Board and has served as a director of the Company since August 2017, effective as of the Merger, and served as a Pre-Merger director of Threshold since June 2002. He is currently the Vice Chancellor of Business Development, Innovation and Partnerships at the University of California, San Francisco, a position that he has held since April 2017. Since January 2023, he has also served as the chief executive officer and a director of Hinge Bio, Inc., a biotechnology company focusing in oncology, inflammatory disease and infectious disease. Previously, Dr. Selick served as Pre-Merger Threshold's Chief Executive Officer from June 2002 until March 2017. Dr. Selick previously served as a director of Amunix Pharmaceuticals, Inc., lead director and chairman of PDL Biopharma, Inc. chairperson of the board of directors of Gyre Therapeuticsa, Inc. (previously Catalyst Biosciences, Inc.) and currently serves as chairperson of the board of Protagonist Therapeutics, Inc.the latter two of which are currently public drug discovery and development companies. Dr. Selick received his B.A. in Biophysics and Ph.D. in Biology from the University of Pennsylvania and was a Damon Runyon-Walter Winchell Cancer Fund Fellow and an American Cancer Society Senior Fellow at the University of California, San Francisco.
Harold E. Selick于2009年8月被选为董事。 Selick博士从2002年6月开始担任Threshold制药股份有限公司(Threshold Pharmaceuticals)的首席执行官兼董事,该公司是一家上市的生物技术公司。从2002年6月到2007年7月,Selick博士还是Sofinnova 风险股份有限公司(Sofinnova Ventures, Inc.)的风险合伙人,该公司是一家风险投资公司。从1999年1月到2002年4月,他担任Camitro股份有限公司( Camitro Corporation)的首席执行官,该公司是一家生物技术公司。从1992年到1999年,他在Affymax研究学院(Affymax Research Institute)任职,这是为葛兰素威康公司(Glaxo Wellcome plc)进行药物研发的技术开发中心,其最后担任的职务是研究部的副总裁。在Affymax任职前,Selick博士在蛋白质设计实验室股份有限公司(Protein Design Labs,现在称为PDL生物制药股份有限公司, PDL BioPharma, Inc.)和Anergen股份有限公司(Anergen, Inc)担任科研职位。作为蛋白质设计实验室股份有限公司的职业科学家,他与人合作发明了一种技术,该技术有潜力开发为完全无排异的抗体疗法,他将其应用于PDL公司的第一个产品——赛尼哌(达利珠单抗),罗氏公司(Roche)将该产品开发并商业化,并将其用于阻止肾移植排异反应。Selick博士担任催化剂生物科学与领导者疗法股份有限公司(Catalyst Biosciences and Protagonist Therapeutics)的董事会主席,该公司是一家私人所有的制药公司。Selick博士在宾夕法尼亚大学获得文学学士学位与博士学位,他还是旧金山加利福尼亚大学的达蒙拉尼恩-沃尔特温切尔癌症基金( Damon Runyon-Walter Winchell Cancer Fund)的研究员和美国癌症协会(American Cancer Society)的高级研究员。
Harold E. Selick,is chairperson of the Board and has served as a director of the Company since August 2017, effective as of the Merger, and served as a Pre-Merger director of Threshold since June 2002. He is currently the Vice Chancellor of Business Development, Innovation and Partnerships at the University of California, San Francisco, a position that he has held since April 2017. Since January 2023, he has also served as the chief executive officer and a director of Hinge Bio, Inc., a biotechnology company focusing in oncology, inflammatory disease and infectious disease. Previously, Dr. Selick served as Pre-Merger Threshold's Chief Executive Officer from June 2002 until March 2017. Dr. Selick previously served as a director of Amunix Pharmaceuticals, Inc., lead director and chairman of PDL Biopharma, Inc. chairperson of the board of directors of Gyre Therapeuticsa, Inc. (previously Catalyst Biosciences, Inc.) and currently serves as chairperson of the board of Protagonist Therapeutics, Inc.the latter two of which are currently public drug discovery and development companies. Dr. Selick received his B.A. in Biophysics and Ph.D. in Biology from the University of Pennsylvania and was a Damon Runyon-Walter Winchell Cancer Fund Fellow and an American Cancer Society Senior Fellow at the University of California, San Francisco.

高管简历

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Eric E. Poma

Eric E. Poma,自2017年8月合并起担任本公司董事。Poma博士是公司的首席执行官兼首席科学官,并于2009年2月创立了Private Molecular,自成立以来一直在其董事会任职。从2005年3月到2008年9月,Poma博士担任Innovive Pharmaceuticals的业务发展副总裁,该公司被一家生物技术公司Innovive Pharmaceuticals收购。从2001年到2005年,他担任ImClone Systems,Inc.(现为副总裁0)的业务发展副副总裁,该公司是一家专注于抗体治疗的生物技术公司。作为Private Molecular的创始人并担任首席科学官,他领导了公司平台技术基础技术的发明,以及构成公司当前主要和临床前管道候选者的全部内容。Poma博士获得了博士学位。在微生物学和免疫学和学士学位在北卡罗来纳大学教堂山分校获得生物学博士学位,在纽约大学获得工商管理硕士学位。Molecular Templates, Inc.董事会得出结论认为,波马博士应担任公司董事,这是基于波马博士直接参与了Molecular Templates公司技术平台的创建和知识以及在该行业的丰富经验,这为Molecular Templates提供了宝贵的洞察力,Inc.董事会讨论涉及公司及其未来目标的事项。


Eric E. Poma,has been a director of the Company since August 2017, effective as of the Merger. Dr. Poma is the Chief Executive Officer and Chief Scientific Officer of the Company and founded Private Molecular in February 2009, serving on its board of directors since its inception. From March 2005 until September 2008, Dr. Poma was Vice President of Business Development of Innovive Pharmaceuticals, Inc. (acquired by Cytrx Corporation), a biotechnology company. As the founder of Private Molecular and in his role as Chief Scientific Officer, he led the invention of technology underlying the Company's platform technology and what constitutes the whole of the Company's current pipeline of candidates. Dr. Poma received his Ph.D. in Microbiology and Immunology and B.S. in Biology from the University of North Carolina at Chapel Hill and his M.B.A. from New York University.
Eric E. Poma,自2017年8月合并起担任本公司董事。Poma博士是公司的首席执行官兼首席科学官,并于2009年2月创立了Private Molecular,自成立以来一直在其董事会任职。从2005年3月到2008年9月,Poma博士担任Innovive Pharmaceuticals的业务发展副总裁,该公司被一家生物技术公司Innovive Pharmaceuticals收购。从2001年到2005年,他担任ImClone Systems,Inc.(现为副总裁0)的业务发展副副总裁,该公司是一家专注于抗体治疗的生物技术公司。作为Private Molecular的创始人并担任首席科学官,他领导了公司平台技术基础技术的发明,以及构成公司当前主要和临床前管道候选者的全部内容。Poma博士获得了博士学位。在微生物学和免疫学和学士学位在北卡罗来纳大学教堂山分校获得生物学博士学位,在纽约大学获得工商管理硕士学位。Molecular Templates, Inc.董事会得出结论认为,波马博士应担任公司董事,这是基于波马博士直接参与了Molecular Templates公司技术平台的创建和知识以及在该行业的丰富经验,这为Molecular Templates提供了宝贵的洞察力,Inc.董事会讨论涉及公司及其未来目标的事项。
Eric E. Poma,has been a director of the Company since August 2017, effective as of the Merger. Dr. Poma is the Chief Executive Officer and Chief Scientific Officer of the Company and founded Private Molecular in February 2009, serving on its board of directors since its inception. From March 2005 until September 2008, Dr. Poma was Vice President of Business Development of Innovive Pharmaceuticals, Inc. (acquired by Cytrx Corporation), a biotechnology company. As the founder of Private Molecular and in his role as Chief Scientific Officer, he led the invention of technology underlying the Company's platform technology and what constitutes the whole of the Company's current pipeline of candidates. Dr. Poma received his Ph.D. in Microbiology and Immunology and B.S. in Biology from the University of North Carolina at Chapel Hill and his M.B.A. from New York University.
Jason S. Kim

Jason S. Kim,本公司总裁兼首席运营官。Kim先生于2010年2月加入Private Molecular,并担任其总裁兼首席财务官直至合并完成。从2009年到2011年,Kim先生担任OSI Pharmaceuticals Now Astellas Pharma US,Inc.的业务和企业发展总监,该公司是一家专注于肿瘤学的生物技术公司。在2009年之前,Kim先生担任Domain Associates,LLC的投资助理,这是一家专注于生物技术行业投资的风险投资公司。从2003年到2006年,Kim先生还担任ImClone Systems Incorporated(现为礼来公司)的业务发展总监,该公司是一家专注于抗体治疗的生物技术公司。金先生获得了学士学位卫斯理大学神经科学与行为学博士,宾夕法尼亚大学沃顿商学院工商管理硕士。


Jason S. Kim,was appointed as the Company's Chief Financial Officer on August 1, 2023 and previously served as the Company's Interim Chief Financial Officer and Chief Operating Officer. Mr. Kim joined Private Molecular in February 2010 and served as its President and Chief Financial Officer until the completion of the Merger. Previously, Mr. Kim served in various corporate development, strategic planning, and commercial roles at OSI Pharmaceuticals, Inc. (now Astellas Pharma US, Inc.) and ImClone Systems, Inc. (now Eli Lilly and Company). Mr. Kim received his B.A. in Neuroscience and Behavior from Wesleyan University and an M.B.A. from the Wharton School, University of Pennsylvania.
Jason S. Kim,本公司总裁兼首席运营官。Kim先生于2010年2月加入Private Molecular,并担任其总裁兼首席财务官直至合并完成。从2009年到2011年,Kim先生担任OSI Pharmaceuticals Now Astellas Pharma US,Inc.的业务和企业发展总监,该公司是一家专注于肿瘤学的生物技术公司。在2009年之前,Kim先生担任Domain Associates,LLC的投资助理,这是一家专注于生物技术行业投资的风险投资公司。从2003年到2006年,Kim先生还担任ImClone Systems Incorporated(现为礼来公司)的业务发展总监,该公司是一家专注于抗体治疗的生物技术公司。金先生获得了学士学位卫斯理大学神经科学与行为学博士,宾夕法尼亚大学沃顿商学院工商管理硕士。
Jason S. Kim,was appointed as the Company's Chief Financial Officer on August 1, 2023 and previously served as the Company's Interim Chief Financial Officer and Chief Operating Officer. Mr. Kim joined Private Molecular in February 2010 and served as its President and Chief Financial Officer until the completion of the Merger. Previously, Mr. Kim served in various corporate development, strategic planning, and commercial roles at OSI Pharmaceuticals, Inc. (now Astellas Pharma US, Inc.) and ImClone Systems, Inc. (now Eli Lilly and Company). Mr. Kim received his B.A. in Neuroscience and Behavior from Wesleyan University and an M.B.A. from the Wharton School, University of Pennsylvania.
Gabriela Gruia

Gabriela Gruia,自2023年5月起担任Aprea Therapeutics公司董事会成员。Gruia博士是一位肿瘤学家,在肿瘤药物开发领域拥有超过25年的经验,涵盖细胞和基因治疗、双特异性、生物制剂、免疫治疗和小分子领域,目前担任Gabriela Gruia咨询有限公司的创始人和负责人。从2020年2月到2021年1月,Gruia博士在Ichnos Sciences担任首席开发官,负责多个关键职能的开发活动,包括临床开发和临床运营、监管科学、临床药理学、毒理学和生物统计学。2004年8月至2020年2月,Gruia博士担任诺华肿瘤学高级副总裁兼全球监管事务主管,领导世界级的肿瘤监管事务组织,并与研究合作者、临床前开发、开发组织和高级管理层密切合作,监督所有监管活动。在诺华期间,Gruia博士领导了多个新分子实体的全球提交和批准,包括Tasigna 、Jakavi 、Afinitor 、Signifor 、Zykadia 、Farydak 、Rydapt 、Odomzo 、Kisqali 、Kymriah 、Adakveo 和Piqray 。Gruia博士是TSCAN Therapeutics、Tessa Therapeutics Ltd.和Molecular Templates, Inc.的董事会成员。Gruia博士在罗马尼亚布加勒斯特医学院获得医学博士学位,在法国巴黎的Rene Huguenin/Curie Institute癌症中心获得乳腺病理学和乳腺摄影硕士学位。她在法国巴黎勒内·笛卡尔大学完成了肿瘤学和血液学的培训。


Gabriela Gruia,has served as a member of board of directors since May 2021. Dr. Gruia founded Gabriela Gruia Consulting, LLC in January 2021. Prior to that, Dr. Gruia served as the Chief Development Officer at Ichnos Sciences Inc. from February 2020 to January 2021, where she oversaw several key functions including Regulatory Sciences, Clinical Operations, Clinical Pharmacology, Biostatistics and Drug Safety. Prior to her time at Ichnos Sciences Inc., Dr. Gruia served as Senior Vice President and Head of Regulatory Affairs for Novartis Oncology from February 2008 through February 2020, where she was responsible for leading the oncology regulatory affairs organization. Dr. Gruia has served on the boards of directors for Aprea Therapeutics, Inc. since 2023, Netris Pharma since 2023, and Molecular Templates, Inc. from March 2022 until its dissolution in December 2024. Dr. Gruia received her doctorate in medicine from Bucharest Medical School in Romania and has a Masters in Breast Pathology and Mammography from Rene Huguenin/Curie Institute Cancer Center in Paris, France. She received her training in oncology and hematology from Rene Descartes University in Paris, France.
Gabriela Gruia,自2023年5月起担任Aprea Therapeutics公司董事会成员。Gruia博士是一位肿瘤学家,在肿瘤药物开发领域拥有超过25年的经验,涵盖细胞和基因治疗、双特异性、生物制剂、免疫治疗和小分子领域,目前担任Gabriela Gruia咨询有限公司的创始人和负责人。从2020年2月到2021年1月,Gruia博士在Ichnos Sciences担任首席开发官,负责多个关键职能的开发活动,包括临床开发和临床运营、监管科学、临床药理学、毒理学和生物统计学。2004年8月至2020年2月,Gruia博士担任诺华肿瘤学高级副总裁兼全球监管事务主管,领导世界级的肿瘤监管事务组织,并与研究合作者、临床前开发、开发组织和高级管理层密切合作,监督所有监管活动。在诺华期间,Gruia博士领导了多个新分子实体的全球提交和批准,包括Tasigna 、Jakavi 、Afinitor 、Signifor 、Zykadia 、Farydak 、Rydapt 、Odomzo 、Kisqali 、Kymriah 、Adakveo 和Piqray 。Gruia博士是TSCAN Therapeutics、Tessa Therapeutics Ltd.和Molecular Templates, Inc.的董事会成员。Gruia博士在罗马尼亚布加勒斯特医学院获得医学博士学位,在法国巴黎的Rene Huguenin/Curie Institute癌症中心获得乳腺病理学和乳腺摄影硕士学位。她在法国巴黎勒内·笛卡尔大学完成了肿瘤学和血液学的培训。
Gabriela Gruia,has served as a member of board of directors since May 2021. Dr. Gruia founded Gabriela Gruia Consulting, LLC in January 2021. Prior to that, Dr. Gruia served as the Chief Development Officer at Ichnos Sciences Inc. from February 2020 to January 2021, where she oversaw several key functions including Regulatory Sciences, Clinical Operations, Clinical Pharmacology, Biostatistics and Drug Safety. Prior to her time at Ichnos Sciences Inc., Dr. Gruia served as Senior Vice President and Head of Regulatory Affairs for Novartis Oncology from February 2008 through February 2020, where she was responsible for leading the oncology regulatory affairs organization. Dr. Gruia has served on the boards of directors for Aprea Therapeutics, Inc. since 2023, Netris Pharma since 2023, and Molecular Templates, Inc. from March 2022 until its dissolution in December 2024. Dr. Gruia received her doctorate in medicine from Bucharest Medical School in Romania and has a Masters in Breast Pathology and Mammography from Rene Huguenin/Curie Institute Cancer Center in Paris, France. She received her training in oncology and hematology from Rene Descartes University in Paris, France.