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 |
|---|---|---|---|---|---|---|
| Robin C. Kramer | 女 | Chair of the Board and Director | 60 | 18.09万美元 | 16.83 | 2026-06-11 |
| Deborah L. Birx | 女 | Chief Executive Officer and Director | 70 | 124.99万美元 | 14.60 | 2026-06-11 |
| Daniel B. Gilmer | 男 | Director | 39 | 未披露 | 未持股 | 2026-06-11 |
| Joseph M. Patti | 男 | Director | 61 | 15.49万美元 | 18.87 | 2026-06-11 |
| Jules Haimovitz | 男 | Director | 75 | 12.89万美元 | 5923.93 | 2026-06-11 |
| Odysseas D. Kostas | 男 | Director | 51 | 13.29万美元 | 5928.77 | 2026-06-11 |
| Sarah J. Schlesinger | 女 | Director | 66 | 14.29万美元 | 5928.77 | 2026-06-11 |
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 |
|---|---|---|---|---|---|---|
| Deborah L. Birx | 女 | Chief Executive Officer and Director | 70 | 124.99万美元 | 14.60 | 2026-06-11 |
| David D. House | 男 | Principal Financial Officer and Senior Vice President, Finance | 42 | 55.48万美元 | 未持股 | 2026-06-11 |
| Pierre Kyme | 男 | Chief Business Officer | 48 | 79.16万美元 | 11.25 | 2026-06-11 |
董事简历
中英对照 |  中文 |  英文- Robin C. Kramer
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Robin C. Kramer,于2018年加入Biogen Inc.,自2020年12月起担任Biogen Inc.高级副总裁、首席会计官。在此之前,Kramer女士于2018年11月至2020年12月担任Biogen Inc.副总裁、首席会计官。在此职位上,她负责监督关键的财务职能,并领导公司的全球业务服务和财务部门。在加入公司之前,Kramer女士曾在Hertz Global Holdings, Inc.、Fisher Scientific International,Inc.和The Gillette Company担任高级财务职务,并曾是Deloitte & Touche LLP、Ernst & Young LLP和Arthur Andersen LLP的审计合伙人。Kramer女士目前担任Armata医药的董事会和审计委员会主席,并担任妇女与企业中心的董事会和财务委员会成员。她拥有Salem State大学会计学学士学位,是Commonwealth of Massachusetts的持牌注册会计师。
Robin C. Kramer was elected as the Company's Chair of the Board in March 2023 and has served as a member of Armata Pharmaceuticals, Inc.'s Board of Directors since December 2020. Ms. Kramer has been appointed as Executive Vice President and Chief Financial Officer at Biogen, a biopharma company, and has served on Biogen's executive committee since March 2025. Prior to this appointment, Ms. Kramer served as Senior Vice President, Chief Accounting Officer and Head of Global Business Services and Treasury of Biogen since January 2021. Ms. Kramer served as Biogen's Vice President, Chief Accounting Officer from November 2018 to December 2020. Prior to joining Biogen, Ms. Kramer served as the Senior Vice President and Chief Accounting Officer of Hertz Global Holdings, Inc., a car rental company, from May 2014 to November 2018. Prior to that, Ms. Kramer was an audit partner at Deloitte & Touche LLP ("Deloitte"), a professional services firm, from 2007 to 2014, including serving in Deloitte's National Office Accounting Standards and Communications Group from 2007 to 2010. From 2005 to 2007, Ms. Kramer served as Chief Accounting Officer of Fisher Scientific International, Inc., a laboratory supply and biotechnology company, and from 2004 to 2005, as Director, External Reporting, Accounting and Control for the Gillette Company, a personal care company. Ms. Kramer has also held partner positions in the public accounting firms of Ernst & Young LLP and Arthur Andersen LLP. Ms. Kramer is a licensed certified public accountant (CPA) in Massachusetts. She is a member of the Massachusetts Society of CPAs and the American Institute of CPAs. She served as a Board member of the Center for Women and Enterprise from August 2020 to December 2024. She previously served as a Board Member of Samsung Bioepis Co., LTD. from July 2020 to April 2022, the Massachusetts State Board of Accountancy from September 2011 to December 2015 and Probus Insurance Company Europe DAC from 2016 to 2018. - Robin C. Kramer,于2018年加入Biogen Inc.,自2020年12月起担任Biogen Inc.高级副总裁、首席会计官。在此之前,Kramer女士于2018年11月至2020年12月担任Biogen Inc.副总裁、首席会计官。在此职位上,她负责监督关键的财务职能,并领导公司的全球业务服务和财务部门。在加入公司之前,Kramer女士曾在Hertz Global Holdings, Inc.、Fisher Scientific International,Inc.和The Gillette Company担任高级财务职务,并曾是Deloitte & Touche LLP、Ernst & Young LLP和Arthur Andersen LLP的审计合伙人。Kramer女士目前担任Armata医药的董事会和审计委员会主席,并担任妇女与企业中心的董事会和财务委员会成员。她拥有Salem State大学会计学学士学位,是Commonwealth of Massachusetts的持牌注册会计师。
- Robin C. Kramer was elected as the Company's Chair of the Board in March 2023 and has served as a member of Armata Pharmaceuticals, Inc.'s Board of Directors since December 2020. Ms. Kramer has been appointed as Executive Vice President and Chief Financial Officer at Biogen, a biopharma company, and has served on Biogen's executive committee since March 2025. Prior to this appointment, Ms. Kramer served as Senior Vice President, Chief Accounting Officer and Head of Global Business Services and Treasury of Biogen since January 2021. Ms. Kramer served as Biogen's Vice President, Chief Accounting Officer from November 2018 to December 2020. Prior to joining Biogen, Ms. Kramer served as the Senior Vice President and Chief Accounting Officer of Hertz Global Holdings, Inc., a car rental company, from May 2014 to November 2018. Prior to that, Ms. Kramer was an audit partner at Deloitte & Touche LLP ("Deloitte"), a professional services firm, from 2007 to 2014, including serving in Deloitte's National Office Accounting Standards and Communications Group from 2007 to 2010. From 2005 to 2007, Ms. Kramer served as Chief Accounting Officer of Fisher Scientific International, Inc., a laboratory supply and biotechnology company, and from 2004 to 2005, as Director, External Reporting, Accounting and Control for the Gillette Company, a personal care company. Ms. Kramer has also held partner positions in the public accounting firms of Ernst & Young LLP and Arthur Andersen LLP. Ms. Kramer is a licensed certified public accountant (CPA) in Massachusetts. She is a member of the Massachusetts Society of CPAs and the American Institute of CPAs. She served as a Board member of the Center for Women and Enterprise from August 2020 to December 2024. She previously served as a Board Member of Samsung Bioepis Co., LTD. from July 2020 to April 2022, the Massachusetts State Board of Accountancy from September 2011 to December 2015 and Probus Insurance Company Europe DAC from 2016 to 2018.
- Deborah L. Birx
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Deborah L. Birx自2023年7月起担任Armata Pharmaceuticals, Inc.的首席执行官。在被任命为公司首席执行官之前,Birx博士于2021年3月辞去了公司最大股东Innoviva, Inc.的董事会成员职务。Birx博士曾担任白宫冠状病毒特别工作组的应对协调员,在那里她向副总统提出建议,利用数据整合来推动决策,并与全国各地的州官员密切合作,提供具体的州建议和指导。2014年,伯克斯博士成为一名在逃大使,当时她担任美国政府抗击艾滋病毒/艾滋病活动协调员和美国全球卫生外交特别代表(每年60亿美元的项目),她在该职位任职至2021年1月。作为美国全球艾滋病协调员,伯克斯博士在疾病预防控制中心监督总统的艾滋病紧急救援计划(PEPFAR),这是历史上任何国家对抗单一疾病的最大承诺,以及美国政府与全球抗击艾滋病、结核病和疟疾基金的所有接触。从2005年到2014年,Birx博士在CDC全球健康中心成功担任CDC全球艾滋病毒/艾滋病(DGHA)司司长,在那里她在全球开发了ISO和CAP认证实验室。从1996年到2005年,她在沃尔特里德陆军研究所担任美国军事HIV研究项目(USMHRP)主任,指导HIV疫苗的研发通过完整的III期试验,包括GLP和GMP制造。在这段时间里,她也升到了上校军衔。当时被称为Birx上校的她在国防部(DOD)任职期间凭借开创性的研究、领导和管理技能,获得了三项享有盛誉的美国立功奖章和军团功勋奖。1985年,Birx博士开始了她在国防部的职业生涯,成为一名受过军事训练的细胞免疫学临床医生,专注于HIV/AIDS疫苗研究。Birx博士在同行评审的期刊上发表了230多篇稿件,在科学出版物中撰写了近十几个章节,还开发了疫苗和专利疫苗。Birx博士目前担任Nanolive SA.Dr董事会成员。伯克斯于1980年获得宾夕法尼亚州立大学赫尔希医学院的医学学位,并于1976年获得霍顿学院的学士学位。Birx博士在内科、过敏和免疫学以及诊断和临床实验室免疫学方面获得董事会认证。Birx博士是世界著名的医学专家和领导者,其长期职业生涯专注于临床和基础免疫学、传染病、大流行防范、疫苗研究和全球健康。
Deborah L. Birx has served as Armata Pharmaceuticals, Inc.'s Chief Executive Officer since July 2023. Prior to her appointment as Chief Executive Officer of the Company, Dr. Birx resigned as a member of the Board of Directors of Innoviva, Inc., the Company's largest shareholder, a position she assumed in March 2021. Dr. Birx served as the response coordinator of the White House Coronavirus Task Force, where she made recommendations to the vice president using data integration to drive decision making, as well as worked closely with state officials across the country to provide state specific advice and guidance. In 2014, Dr. Birx became an Ambassador at Large, when she assumed the role of the Coordinator of the United States Government Activities to Combat HIV/AIDS and U.S. Special Representative for Global Health Diplomacy (a $6 billion per year program), a position she served in until January 2021. As the U.S. Global AIDS Coordinator, Dr. Birx oversaw the President's Emergency Plan for AIDS Relief (PEPFAR), the largest commitment by any nation to combat a single disease in history, at the CDC as well as all U.S. Government engagement with the Global Fund to Fight AIDS, Tuberculosis and Malaria. From 2005 until 2014, Dr. Birx served successfully as the Director of CDC's Division of Global HIV/AIDS (DGHA) in the CDC Center for Global Health where she developed ISO and CAP certified laboratories across the globe. From 1996 until 2005, she served as the Director of the U.S. Military HIV Research Program (USMHRP) at the Walter Reed Army Institute of Research directing research and development of HIV vaccines through full Phase III trials, including GLP and GMP manufacturing. During this time, she also rose to the rank of Colonel. Then known as Colonel Birx, she was awarded three prestigious U.S. Meritorious Service Medals and the Legion of Merit Award for her groundbreaking research, leadership and management skills during her tenure at the Department of Defense (DoD). In 1985, Dr. Birx began her career with the DoD as a military trained clinician in cellular immunology, focusing on HIV/AIDS vaccine research. Dr. Birx has published over 230 manuscripts in peer reviewed journals, authored nearly a dozen chapters in scientific publications, as well as developed and patented vaccines. Dr. Birx currently serves as a member of the Board of Directors of Nanolive SA.Dr. Birx received her medical degree from the Hershey School of Medicine, Pennsylvania State University in 1980 and her B.S. from Houghton College in 1976. Dr. Birx is board certified in internal medicine, allergy and immunology, and diagnostic and clinical laboratory immunology. Dr. Birx is a world renowned medical expert and leader whose long career has focused on clinical and basic immunology, infectious diseases, pandemic preparedness, vaccine research, and global health. - Deborah L. Birx自2023年7月起担任Armata Pharmaceuticals, Inc.的首席执行官。在被任命为公司首席执行官之前,Birx博士于2021年3月辞去了公司最大股东Innoviva, Inc.的董事会成员职务。Birx博士曾担任白宫冠状病毒特别工作组的应对协调员,在那里她向副总统提出建议,利用数据整合来推动决策,并与全国各地的州官员密切合作,提供具体的州建议和指导。2014年,伯克斯博士成为一名在逃大使,当时她担任美国政府抗击艾滋病毒/艾滋病活动协调员和美国全球卫生外交特别代表(每年60亿美元的项目),她在该职位任职至2021年1月。作为美国全球艾滋病协调员,伯克斯博士在疾病预防控制中心监督总统的艾滋病紧急救援计划(PEPFAR),这是历史上任何国家对抗单一疾病的最大承诺,以及美国政府与全球抗击艾滋病、结核病和疟疾基金的所有接触。从2005年到2014年,Birx博士在CDC全球健康中心成功担任CDC全球艾滋病毒/艾滋病(DGHA)司司长,在那里她在全球开发了ISO和CAP认证实验室。从1996年到2005年,她在沃尔特里德陆军研究所担任美国军事HIV研究项目(USMHRP)主任,指导HIV疫苗的研发通过完整的III期试验,包括GLP和GMP制造。在这段时间里,她也升到了上校军衔。当时被称为Birx上校的她在国防部(DOD)任职期间凭借开创性的研究、领导和管理技能,获得了三项享有盛誉的美国立功奖章和军团功勋奖。1985年,Birx博士开始了她在国防部的职业生涯,成为一名受过军事训练的细胞免疫学临床医生,专注于HIV/AIDS疫苗研究。Birx博士在同行评审的期刊上发表了230多篇稿件,在科学出版物中撰写了近十几个章节,还开发了疫苗和专利疫苗。Birx博士目前担任Nanolive SA.Dr董事会成员。伯克斯于1980年获得宾夕法尼亚州立大学赫尔希医学院的医学学位,并于1976年获得霍顿学院的学士学位。Birx博士在内科、过敏和免疫学以及诊断和临床实验室免疫学方面获得董事会认证。Birx博士是世界著名的医学专家和领导者,其长期职业生涯专注于临床和基础免疫学、传染病、大流行防范、疫苗研究和全球健康。
- Deborah L. Birx has served as Armata Pharmaceuticals, Inc.'s Chief Executive Officer since July 2023. Prior to her appointment as Chief Executive Officer of the Company, Dr. Birx resigned as a member of the Board of Directors of Innoviva, Inc., the Company's largest shareholder, a position she assumed in March 2021. Dr. Birx served as the response coordinator of the White House Coronavirus Task Force, where she made recommendations to the vice president using data integration to drive decision making, as well as worked closely with state officials across the country to provide state specific advice and guidance. In 2014, Dr. Birx became an Ambassador at Large, when she assumed the role of the Coordinator of the United States Government Activities to Combat HIV/AIDS and U.S. Special Representative for Global Health Diplomacy (a $6 billion per year program), a position she served in until January 2021. As the U.S. Global AIDS Coordinator, Dr. Birx oversaw the President's Emergency Plan for AIDS Relief (PEPFAR), the largest commitment by any nation to combat a single disease in history, at the CDC as well as all U.S. Government engagement with the Global Fund to Fight AIDS, Tuberculosis and Malaria. From 2005 until 2014, Dr. Birx served successfully as the Director of CDC's Division of Global HIV/AIDS (DGHA) in the CDC Center for Global Health where she developed ISO and CAP certified laboratories across the globe. From 1996 until 2005, she served as the Director of the U.S. Military HIV Research Program (USMHRP) at the Walter Reed Army Institute of Research directing research and development of HIV vaccines through full Phase III trials, including GLP and GMP manufacturing. During this time, she also rose to the rank of Colonel. Then known as Colonel Birx, she was awarded three prestigious U.S. Meritorious Service Medals and the Legion of Merit Award for her groundbreaking research, leadership and management skills during her tenure at the Department of Defense (DoD). In 1985, Dr. Birx began her career with the DoD as a military trained clinician in cellular immunology, focusing on HIV/AIDS vaccine research. Dr. Birx has published over 230 manuscripts in peer reviewed journals, authored nearly a dozen chapters in scientific publications, as well as developed and patented vaccines. Dr. Birx currently serves as a member of the Board of Directors of Nanolive SA.Dr. Birx received her medical degree from the Hershey School of Medicine, Pennsylvania State University in 1980 and her B.S. from Houghton College in 1976. Dr. Birx is board certified in internal medicine, allergy and immunology, and diagnostic and clinical laboratory immunology. Dr. Birx is a world renowned medical expert and leader whose long career has focused on clinical and basic immunology, infectious diseases, pandemic preparedness, vaccine research, and global health.
- Daniel B. Gilmer
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Daniel B. Gilmer自2026年4月起在Armata Pharmaceuticals, Inc.董事会任职。Gilmer博士自2025年2月起在辉瑞公司(“辉瑞”)担任高级总监、商业质量美国团队负责人。在辉瑞,他领导着一个负责50多个美国品牌的质量和促销审查的组织。他的团队与医疗、法律和监管主题专家密切合作,就内容质量、合规性和风险收益平衡向商业利益相关者提供建议。此前,从2022年4月到2025年2月,Gilmer博士在辉瑞的抗病毒和诊断业务中领导跨职能团队,在那里他在美国推出了PAXLOVIDTM,因为它获得了美国食品和药物管理局(“FDA”)的新药批准。在辉瑞任职的更早时间,从2021年4月到2022年4月,Gilmer博士在炎症与免疫学商业开发部门工作,在那里他帮助制定了风湿病学和免疫学资产组合的战略。Gilmer博士于2019年5月加入辉瑞从事研发工作,为辉瑞的COVID 19疫苗使能运营模式和研发组合战略做出贡献。吉尔默博士是Exebacase(也称为“CF301”或“PLYSS2”)专利的平等共同发明人,这是一种链球菌噬菌体溶酶。在推进3期临床试验之前,Exebacase获得了FDA的快速通道和突破性疗法指定。吉尔默博士撰写了多篇关于噬菌体溶素和抗菌素耐药性的同行评审出版物。在加入辉瑞之前,Gilmer博士曾任职于麦肯锡公司,专注于美国、加拿大和法国的商业增长战略、市场准入以及精益制造。在他职业生涯的早期,他曾在领先的学术机构和美国国立卫生研究院进行微生物学和传染病研究。他拥有洛克菲勒大学(RU)微生物学博士学位和霍华德大学学士学位。作为RU校友,他同时担任RU董事会教育事务委员会和RU Ford中心孵化器遴选委员会成员。他是纽约科学院的成员,也是外交关系委员会的长期成员。
Daniel B. Gilmer has served on Armata Pharmaceuticals, Inc.'s Board of Directors since April 2026. Dr. Gilmer has served as Senior Director, Commercial Quality US Team Lead at Pfizer Inc. ("Pfizer") since February 2025. At Pfizer, he leads an organization responsible for quality and promotional review across 50+ U.S. brands. His team works closely with medical, legal, and regulatory subject matter experts to advise commercial stakeholders on content quality, compliance, and risk benefit balance. Previously, from April 2022 to February 2025, Dr. Gilmer led cross functional teams in Pfizer's Antiviral and Diagnostics Business, where he launched PAXLOVIDTM in the United States as it received New Drug Approval from the U.S. Food and Drug Administration (the "FDA"). Earlier at Pfizer, from April 2021 to April 2022, Dr. Gilmer worked in Inflammation & Immunology Commercial Development, where he helped shape strategy for a portfolio of rheumatology and immunology assets. Dr. Gilmer joined Pfizer in Research & Development in May 2019, where he contributed to Pfizer's COVID 19 vaccine enabling operating model and R&D portfolio strategy. Dr. Gilmer is an equal co inventor on the patent for Exebacase (also termed "CF 301" or "PlySs2"), a first in class Streptococcus bacteriophage lysin. Exebacase received Fast Track and Breakthrough Therapy designations from the FDA before advancing to Phase 3 clinical trials. Dr. Gilmer has authored multiple peer reviewed publications on phage lysins and antimicrobial resistance. Prior to joining Pfizer, Dr. Gilmer worked at McKinsey & Co. focusing on commercial growth strategies, market access, and lean manufacturing in the United States, Canada, and France. Earlier in his career, he conducted microbiology and infectious disease research at leading academic institutions and the National Institutes of Health. He has a Ph.D. in Microbiology from Rockefeller University (RU) and a B.S. from Howard University. As an RU alum, he serves on both the RU Board of Trustees Educational Affairs Committee and the RU Ford Center Incubator selection committee. He is a member of the New York Academy of Sciences and a term member at the Council on Foreign Relations. - Daniel B. Gilmer自2026年4月起在Armata Pharmaceuticals, Inc.董事会任职。Gilmer博士自2025年2月起在辉瑞公司(“辉瑞”)担任高级总监、商业质量美国团队负责人。在辉瑞,他领导着一个负责50多个美国品牌的质量和促销审查的组织。他的团队与医疗、法律和监管主题专家密切合作,就内容质量、合规性和风险收益平衡向商业利益相关者提供建议。此前,从2022年4月到2025年2月,Gilmer博士在辉瑞的抗病毒和诊断业务中领导跨职能团队,在那里他在美国推出了PAXLOVIDTM,因为它获得了美国食品和药物管理局(“FDA”)的新药批准。在辉瑞任职的更早时间,从2021年4月到2022年4月,Gilmer博士在炎症与免疫学商业开发部门工作,在那里他帮助制定了风湿病学和免疫学资产组合的战略。Gilmer博士于2019年5月加入辉瑞从事研发工作,为辉瑞的COVID 19疫苗使能运营模式和研发组合战略做出贡献。吉尔默博士是Exebacase(也称为“CF301”或“PLYSS2”)专利的平等共同发明人,这是一种链球菌噬菌体溶酶。在推进3期临床试验之前,Exebacase获得了FDA的快速通道和突破性疗法指定。吉尔默博士撰写了多篇关于噬菌体溶素和抗菌素耐药性的同行评审出版物。在加入辉瑞之前,Gilmer博士曾任职于麦肯锡公司,专注于美国、加拿大和法国的商业增长战略、市场准入以及精益制造。在他职业生涯的早期,他曾在领先的学术机构和美国国立卫生研究院进行微生物学和传染病研究。他拥有洛克菲勒大学(RU)微生物学博士学位和霍华德大学学士学位。作为RU校友,他同时担任RU董事会教育事务委员会和RU Ford中心孵化器遴选委员会成员。他是纽约科学院的成员,也是外交关系委员会的长期成员。
- Daniel B. Gilmer has served on Armata Pharmaceuticals, Inc.'s Board of Directors since April 2026. Dr. Gilmer has served as Senior Director, Commercial Quality US Team Lead at Pfizer Inc. ("Pfizer") since February 2025. At Pfizer, he leads an organization responsible for quality and promotional review across 50+ U.S. brands. His team works closely with medical, legal, and regulatory subject matter experts to advise commercial stakeholders on content quality, compliance, and risk benefit balance. Previously, from April 2022 to February 2025, Dr. Gilmer led cross functional teams in Pfizer's Antiviral and Diagnostics Business, where he launched PAXLOVIDTM in the United States as it received New Drug Approval from the U.S. Food and Drug Administration (the "FDA"). Earlier at Pfizer, from April 2021 to April 2022, Dr. Gilmer worked in Inflammation & Immunology Commercial Development, where he helped shape strategy for a portfolio of rheumatology and immunology assets. Dr. Gilmer joined Pfizer in Research & Development in May 2019, where he contributed to Pfizer's COVID 19 vaccine enabling operating model and R&D portfolio strategy. Dr. Gilmer is an equal co inventor on the patent for Exebacase (also termed "CF 301" or "PlySs2"), a first in class Streptococcus bacteriophage lysin. Exebacase received Fast Track and Breakthrough Therapy designations from the FDA before advancing to Phase 3 clinical trials. Dr. Gilmer has authored multiple peer reviewed publications on phage lysins and antimicrobial resistance. Prior to joining Pfizer, Dr. Gilmer worked at McKinsey & Co. focusing on commercial growth strategies, market access, and lean manufacturing in the United States, Canada, and France. Earlier in his career, he conducted microbiology and infectious disease research at leading academic institutions and the National Institutes of Health. He has a Ph.D. in Microbiology from Rockefeller University (RU) and a B.S. from Howard University. As an RU alum, he serves on both the RU Board of Trustees Educational Affairs Committee and the RU Ford Center Incubator selection committee. He is a member of the New York Academy of Sciences and a term member at the Council on Foreign Relations.
- Joseph M. Patti
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Joseph M. Patti,2007年起,他担任首席科技官和研发高级副总裁;1998至2007年,担任公司临床前开发副总裁和首席科技官;2005至2007年担任研发副总裁。1994至1998年,他担任德克萨斯农工大学(Texas A&M)生物科学与技术系的副教授。1996至1998年,他还曾担任德克萨斯大学(University of Texas)健康科学中心生物医学研究所的教师。他在匹茨堡大学(University of Pittsburgh)获得微生物学学士学位,在迈阿密大学医学院(University of Miami, School of Medicine)获得公共卫生学硕士学位,在伯明翰阿拉巴马大学(University of Alabama)获得生物化学博士学位。
Joseph M. Patti has served as a member of Armata Pharmaceuticals, Inc.'s Board of Directors since the consummation of the Merger in May 2019. Since February 2018, Dr. Patti has been the President of JB Biotech Advisors, Inc., which provides strategic growth and drug development advice to emerging biotechnology companies. Since April 2024, Dr. Patti has been the President, Chief Executive Officer, and director of FibroNox, Inc. From June 2022 to June 2023, Dr. Patti served as a director and President and Chief Executive Officer of Evecxia Therapeutics, Inc. Dr. Patti was Executive Chairman of AgilVax, Inc. from November 2018 to August 2019, when he was appointed President and Chief Executive Officer and director and served in such positions until July 2021. Dr. Patti served as Aviragen Therapeutics, Inc.'s Executive Vice President of Corporate Development and Strategy from November 2012 to October 2014, when he was appointed as a director and President and Chief Executive Officer of the company. He served in those roles until February 2018, when Aviragen merged with Vaxart, Inc. Before joining Aviragen, Dr. Patti co founded Inhibitex, Inc. in 1994 and served as its Chief Scientific Officer and Senior Vice President of Research and Development from 2007 until Bristol Myers Squibb acquired it in February 2012. He also served as its Chief Scientific Officer and Vice President of Research and Development from 2005 to 2007 and as Vice President of Preclinical Development. Dr. Patti was a director of Inhibitex from 1998 to 2005. Before co founding Inhibitex, Dr. Patti was an Assistant Professor at Texas A&M's Institute of Biosciences and Technology and served on the faculty at the University of Texas Health Science Center Graduate School of Biomedical Sciences. Dr. Patti received a B.S. in Microbiology from the University of Pittsburgh, an M.S.P.H. from the University of Miami School of Medicine, and a Ph.D. in Biochemistry from the University of Alabama at Birmingham. Dr. Patti was a director of SciStem Therapeutics, Inc., a privately held biotechnology company, from 2012 to 2015. - Joseph M. Patti,2007年起,他担任首席科技官和研发高级副总裁;1998至2007年,担任公司临床前开发副总裁和首席科技官;2005至2007年担任研发副总裁。1994至1998年,他担任德克萨斯农工大学(Texas A&M)生物科学与技术系的副教授。1996至1998年,他还曾担任德克萨斯大学(University of Texas)健康科学中心生物医学研究所的教师。他在匹茨堡大学(University of Pittsburgh)获得微生物学学士学位,在迈阿密大学医学院(University of Miami, School of Medicine)获得公共卫生学硕士学位,在伯明翰阿拉巴马大学(University of Alabama)获得生物化学博士学位。
- Joseph M. Patti has served as a member of Armata Pharmaceuticals, Inc.'s Board of Directors since the consummation of the Merger in May 2019. Since February 2018, Dr. Patti has been the President of JB Biotech Advisors, Inc., which provides strategic growth and drug development advice to emerging biotechnology companies. Since April 2024, Dr. Patti has been the President, Chief Executive Officer, and director of FibroNox, Inc. From June 2022 to June 2023, Dr. Patti served as a director and President and Chief Executive Officer of Evecxia Therapeutics, Inc. Dr. Patti was Executive Chairman of AgilVax, Inc. from November 2018 to August 2019, when he was appointed President and Chief Executive Officer and director and served in such positions until July 2021. Dr. Patti served as Aviragen Therapeutics, Inc.'s Executive Vice President of Corporate Development and Strategy from November 2012 to October 2014, when he was appointed as a director and President and Chief Executive Officer of the company. He served in those roles until February 2018, when Aviragen merged with Vaxart, Inc. Before joining Aviragen, Dr. Patti co founded Inhibitex, Inc. in 1994 and served as its Chief Scientific Officer and Senior Vice President of Research and Development from 2007 until Bristol Myers Squibb acquired it in February 2012. He also served as its Chief Scientific Officer and Vice President of Research and Development from 2005 to 2007 and as Vice President of Preclinical Development. Dr. Patti was a director of Inhibitex from 1998 to 2005. Before co founding Inhibitex, Dr. Patti was an Assistant Professor at Texas A&M's Institute of Biosciences and Technology and served on the faculty at the University of Texas Health Science Center Graduate School of Biomedical Sciences. Dr. Patti received a B.S. in Microbiology from the University of Pittsburgh, an M.S.P.H. from the University of Miami School of Medicine, and a Ph.D. in Biochemistry from the University of Alabama at Birmingham. Dr. Patti was a director of SciStem Therapeutics, Inc., a privately held biotechnology company, from 2012 to 2015.
- Jules Haimovitz
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Jules Haimovitz自2005年Blucora担任Blucora董事。自2007年7月,他担任Haimovitz顾问公司的总裁,该公司是媒体顾问公司。从2002年7月至2007年7月, Mr. Haimovitz担任 Dick Clark Productions有限公司的副董事长和管理合伙人,该公司从事电视、电缆网络、访问权项目供应。从1999年6月至2004年7月,Mr. Haimovitz担任Metro Goldwyn Mayer有限公司的多种职位。Mr. Haimovitz有很多经验,还担任VJN有限公司的首席执行官、Spelling娱乐有限公司的执行主管,King World Productions and Viacom有限公司的主管,Orion Pictures Corporation and Onstage娱乐公司的主管。Mr. Haimovitz从2007年5月至2008年11月担任Imclone公司的主管,从2006年5月至2011年4月担任Blockbuster的主管。Mr. Haimovitz自2011年11月担任Dial Global前身Westwood One有限公司的主管,担任审计委员会主席。
Jules Haimovitz has served as a member of Armata Pharmaceuticals, Inc.'s Board of Directors since April 2021, and served as the Company's Chairman of the Board between June 2021 and March 2023. At Innoviva, Inc. (NASDAQ: INVA), Mr. Haimovitz has served as a member of the board of directors since February 2018. Mr. Haimovitz is currently President of Haimovitz Consulting, Inc. He previously served as a member of the board of directors of Ariad Pharmaceuticals, where he was also a member of its audit committee; Dial Global, Inc., where he was also member of its audit committee; and Imclone Pharmaceuticals, where he served as chairperson of its audit committee. Mr. Haimovitz has also served as Chief Executive Officer or Chief Operating Officer of the following companies: Spelling Entertainment, Inc., King World Productions and VJN, Inc. Mr. Haimovitz holds a B.S. and M.A. degree in Mathematics from Brooklyn College. - Jules Haimovitz自2005年Blucora担任Blucora董事。自2007年7月,他担任Haimovitz顾问公司的总裁,该公司是媒体顾问公司。从2002年7月至2007年7月, Mr. Haimovitz担任 Dick Clark Productions有限公司的副董事长和管理合伙人,该公司从事电视、电缆网络、访问权项目供应。从1999年6月至2004年7月,Mr. Haimovitz担任Metro Goldwyn Mayer有限公司的多种职位。Mr. Haimovitz有很多经验,还担任VJN有限公司的首席执行官、Spelling娱乐有限公司的执行主管,King World Productions and Viacom有限公司的主管,Orion Pictures Corporation and Onstage娱乐公司的主管。Mr. Haimovitz从2007年5月至2008年11月担任Imclone公司的主管,从2006年5月至2011年4月担任Blockbuster的主管。Mr. Haimovitz自2011年11月担任Dial Global前身Westwood One有限公司的主管,担任审计委员会主席。
- Jules Haimovitz has served as a member of Armata Pharmaceuticals, Inc.'s Board of Directors since April 2021, and served as the Company's Chairman of the Board between June 2021 and March 2023. At Innoviva, Inc. (NASDAQ: INVA), Mr. Haimovitz has served as a member of the board of directors since February 2018. Mr. Haimovitz is currently President of Haimovitz Consulting, Inc. He previously served as a member of the board of directors of Ariad Pharmaceuticals, where he was also a member of its audit committee; Dial Global, Inc., where he was also member of its audit committee; and Imclone Pharmaceuticals, where he served as chairperson of its audit committee. Mr. Haimovitz has also served as Chief Executive Officer or Chief Operating Officer of the following companies: Spelling Entertainment, Inc., King World Productions and VJN, Inc. Mr. Haimovitz holds a B.S. and M.A. degree in Mathematics from Brooklyn College.
- Odysseas D. Kostas
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Odysseas D. Kostas,医学博士,自2020年2月起担任Armata制药公司董事会成员。他目前还担任Innoviva, Inc.的董事。他是Sarissa Capital Management LP的合伙人兼高级董事总经理。Sarissa Capital专注于改善公司战略,以提高股东价值。在加入Sarissa Capital之前,Kostas博士曾担任Evercore ISI(前身为ISI)的董事,负责生物技术和制药行业。在此之前,他作为耶鲁大学纽黑文卫生系统的一部分从事内科工作,并被聘为多家生物技术公司的顾问。Kostas博士也曾在Enzon制药公司董事会任职。Kostas博士拥有麻省理工学院(MIT)的学士学位和德克萨斯大学西南医学院的医学博士学位。Kostas博士在他的领域表现出了领导能力,他对Armata Pharmaceuticals,Inc.行业的了解和经验促使Armata Pharmaceuticals,Inc.得出结论,认为他应该担任董事。
Odysseas D. Kostas has served as a member of Armata Pharmaceuticals, Inc.'s Board of Directors since February 2020. He also currently serves as director and Chairman of Amarin Corporation. Dr. Kostas is founder and Managing Director of Polymetis Strategies LLC, a consulting firm focused on finance, strategy, and operations. He serves as an advisor to Sarissa Capital Management LP where he previously served as a Partner, Senior Managing Director, and Head of Research. Prior to joining Sarissa Capital, Dr. Kostas served as a Director at Evercore ISI (formerly ISI), covering the biotechnology and pharmaceutical industries. Previously, he practiced internal medicine as part of the Yale New Haven Health System and was engaged as a consultant to various biotechnology companies. Dr. Kostas also previously served on the board of directors of Innoviva and Enzon Pharmaceuticals.Dr. Kostas has a B.S from Massachusetts Institute of Technology (MIT) and an M.D. from the University of Texas Southwestern Medical School. - Odysseas D. Kostas,医学博士,自2020年2月起担任Armata制药公司董事会成员。他目前还担任Innoviva, Inc.的董事。他是Sarissa Capital Management LP的合伙人兼高级董事总经理。Sarissa Capital专注于改善公司战略,以提高股东价值。在加入Sarissa Capital之前,Kostas博士曾担任Evercore ISI(前身为ISI)的董事,负责生物技术和制药行业。在此之前,他作为耶鲁大学纽黑文卫生系统的一部分从事内科工作,并被聘为多家生物技术公司的顾问。Kostas博士也曾在Enzon制药公司董事会任职。Kostas博士拥有麻省理工学院(MIT)的学士学位和德克萨斯大学西南医学院的医学博士学位。Kostas博士在他的领域表现出了领导能力,他对Armata Pharmaceuticals,Inc.行业的了解和经验促使Armata Pharmaceuticals,Inc.得出结论,认为他应该担任董事。
- Odysseas D. Kostas has served as a member of Armata Pharmaceuticals, Inc.'s Board of Directors since February 2020. He also currently serves as director and Chairman of Amarin Corporation. Dr. Kostas is founder and Managing Director of Polymetis Strategies LLC, a consulting firm focused on finance, strategy, and operations. He serves as an advisor to Sarissa Capital Management LP where he previously served as a Partner, Senior Managing Director, and Head of Research. Prior to joining Sarissa Capital, Dr. Kostas served as a Director at Evercore ISI (formerly ISI), covering the biotechnology and pharmaceutical industries. Previously, he practiced internal medicine as part of the Yale New Haven Health System and was engaged as a consultant to various biotechnology companies. Dr. Kostas also previously served on the board of directors of Innoviva and Enzon Pharmaceuticals.Dr. Kostas has a B.S from Massachusetts Institute of Technology (MIT) and an M.D. from the University of Texas Southwestern Medical School.
- Sarah J. Schlesinger
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Sarah J. Schlesinger医学博士在细胞免疫领域工作了20多年,担任过由Ralph M. Steinman医学博士领导的实验室的主任,或得了2011年诺贝尔生理医学奖。她目前是洛克菲勒大学细胞生理学和免疫学实验室的高级主治医生和临床研究副教授。2002年到2003年,在加入洛克菲勒大学前,她是纽约国际艾滋病疫苗行动组织一个科学家。1996年到2002年,她是 Walter Reed Army Institute of Research的医学、病理学家,作为Armed Force Institute of Pathology 员工住在华盛顿特区。她在华盛顿乔治敦大学爱因斯坦医学院开始她外科手术的职业生涯,并在纽约多家医院包括Buffalo General,、Hospital New York和 the Manhattan Eye, Ear and Throat Hospital工作过。她取得了韦尔斯利学院学位和芝加哥拉什医学院的医学博士学位。
Sarah J. Schlesinger has served as a member of Armata Pharmaceuticals, Inc.'s Board of Directors since February 2020. She also currently serves as a member of the board of directors of Innoviva, Inc. and serves on its Compensation Committee and as chairperson of its Nominating/Corporate Governance Committee. Dr. Schlesinger is an Associate Professor of Clinical Investigation at Rockefeller University and Senior Attending Physician at Rockefeller University Hospital. She is also President of the Rockefeller University Medical Staff. Dr. Schlesinger was the Clinical Director of the laboratory of Dr. Ralph Steinman (Nobel Laureate 2011) from 2002 until his death in 2011. Dr. Schlesinger led the Dendritic Cell section of the Division of Retrovirology at the Walter Reed Army Institute of Research and was also a member of the Division of Infectious and Parasitic Disease Pathology at the Armed Forces Institute of Pathology from 1994 to 2002. In 2002, Dr. Schlesinger rejoined Rockefeller University and began working with the International AIDS Vaccine Initiative as a Scientist in Vaccine Research and Design. Dr. Schlesinger has been a member of Rockefeller University Hospital's Institutional Review Board ("IRB") (Ethics Committee) since 2003 and previously served as IRB's vice chairperson. In 2017, Dr. Schlesinger assumed the position of chairperson of the IRB. She is currently the director of the education and training programs at Rockefeller University Center for Clinical and Translational Science and serves on the Medical Staff Executive Committee of Rockefeller University Hospital. Dr. Schlesinger previously served on the board of three non profit organizations: the AIDS Vaccines Advocacy Coalition, Global Viral and The Hastings Center, the pre eminent center for the study of bioethics. Dr. Schlesinger currently serves on the board of the Albert Einstein College of Medicine. Dr. Schlesinger served as an independent corporate director of Ariad Pharmaceuticals from 2013 until its sale to Takeda Pharmaceutical Company Limited in 2017. She also served as an independent corporate director of The Medicines Company from 2018 until its acquisition by Novartis in 2020. Dr. Schlesinger has a B.A. from Wellesley College and an M.D. from Rush Medical College in Chicago, Illinois. She trained in Anatomic Pathology at The New York Hospital where she served as Chief Resident. - Sarah J. Schlesinger医学博士在细胞免疫领域工作了20多年,担任过由Ralph M. Steinman医学博士领导的实验室的主任,或得了2011年诺贝尔生理医学奖。她目前是洛克菲勒大学细胞生理学和免疫学实验室的高级主治医生和临床研究副教授。2002年到2003年,在加入洛克菲勒大学前,她是纽约国际艾滋病疫苗行动组织一个科学家。1996年到2002年,她是 Walter Reed Army Institute of Research的医学、病理学家,作为Armed Force Institute of Pathology 员工住在华盛顿特区。她在华盛顿乔治敦大学爱因斯坦医学院开始她外科手术的职业生涯,并在纽约多家医院包括Buffalo General,、Hospital New York和 the Manhattan Eye, Ear and Throat Hospital工作过。她取得了韦尔斯利学院学位和芝加哥拉什医学院的医学博士学位。
- Sarah J. Schlesinger has served as a member of Armata Pharmaceuticals, Inc.'s Board of Directors since February 2020. She also currently serves as a member of the board of directors of Innoviva, Inc. and serves on its Compensation Committee and as chairperson of its Nominating/Corporate Governance Committee. Dr. Schlesinger is an Associate Professor of Clinical Investigation at Rockefeller University and Senior Attending Physician at Rockefeller University Hospital. She is also President of the Rockefeller University Medical Staff. Dr. Schlesinger was the Clinical Director of the laboratory of Dr. Ralph Steinman (Nobel Laureate 2011) from 2002 until his death in 2011. Dr. Schlesinger led the Dendritic Cell section of the Division of Retrovirology at the Walter Reed Army Institute of Research and was also a member of the Division of Infectious and Parasitic Disease Pathology at the Armed Forces Institute of Pathology from 1994 to 2002. In 2002, Dr. Schlesinger rejoined Rockefeller University and began working with the International AIDS Vaccine Initiative as a Scientist in Vaccine Research and Design. Dr. Schlesinger has been a member of Rockefeller University Hospital's Institutional Review Board ("IRB") (Ethics Committee) since 2003 and previously served as IRB's vice chairperson. In 2017, Dr. Schlesinger assumed the position of chairperson of the IRB. She is currently the director of the education and training programs at Rockefeller University Center for Clinical and Translational Science and serves on the Medical Staff Executive Committee of Rockefeller University Hospital. Dr. Schlesinger previously served on the board of three non profit organizations: the AIDS Vaccines Advocacy Coalition, Global Viral and The Hastings Center, the pre eminent center for the study of bioethics. Dr. Schlesinger currently serves on the board of the Albert Einstein College of Medicine. Dr. Schlesinger served as an independent corporate director of Ariad Pharmaceuticals from 2013 until its sale to Takeda Pharmaceutical Company Limited in 2017. She also served as an independent corporate director of The Medicines Company from 2018 until its acquisition by Novartis in 2020. Dr. Schlesinger has a B.A. from Wellesley College and an M.D. from Rush Medical College in Chicago, Illinois. She trained in Anatomic Pathology at The New York Hospital where she served as Chief Resident.
高管简历
中英对照 |  中文 |  英文- Deborah L. Birx
Deborah L. Birx自2023年7月起担任Armata Pharmaceuticals, Inc.的首席执行官。在被任命为公司首席执行官之前,Birx博士于2021年3月辞去了公司最大股东Innoviva, Inc.的董事会成员职务。Birx博士曾担任白宫冠状病毒特别工作组的应对协调员,在那里她向副总统提出建议,利用数据整合来推动决策,并与全国各地的州官员密切合作,提供具体的州建议和指导。2014年,伯克斯博士成为一名在逃大使,当时她担任美国政府抗击艾滋病毒/艾滋病活动协调员和美国全球卫生外交特别代表(每年60亿美元的项目),她在该职位任职至2021年1月。作为美国全球艾滋病协调员,伯克斯博士在疾病预防控制中心监督总统的艾滋病紧急救援计划(PEPFAR),这是历史上任何国家对抗单一疾病的最大承诺,以及美国政府与全球抗击艾滋病、结核病和疟疾基金的所有接触。从2005年到2014年,Birx博士在CDC全球健康中心成功担任CDC全球艾滋病毒/艾滋病(DGHA)司司长,在那里她在全球开发了ISO和CAP认证实验室。从1996年到2005年,她在沃尔特里德陆军研究所担任美国军事HIV研究项目(USMHRP)主任,指导HIV疫苗的研发通过完整的III期试验,包括GLP和GMP制造。在这段时间里,她也升到了上校军衔。当时被称为Birx上校的她在国防部(DOD)任职期间凭借开创性的研究、领导和管理技能,获得了三项享有盛誉的美国立功奖章和军团功勋奖。1985年,Birx博士开始了她在国防部的职业生涯,成为一名受过军事训练的细胞免疫学临床医生,专注于HIV/AIDS疫苗研究。Birx博士在同行评审的期刊上发表了230多篇稿件,在科学出版物中撰写了近十几个章节,还开发了疫苗和专利疫苗。Birx博士目前担任Nanolive SA.Dr董事会成员。伯克斯于1980年获得宾夕法尼亚州立大学赫尔希医学院的医学学位,并于1976年获得霍顿学院的学士学位。Birx博士在内科、过敏和免疫学以及诊断和临床实验室免疫学方面获得董事会认证。Birx博士是世界著名的医学专家和领导者,其长期职业生涯专注于临床和基础免疫学、传染病、大流行防范、疫苗研究和全球健康。
Deborah L. Birx has served as Armata Pharmaceuticals, Inc.'s Chief Executive Officer since July 2023. Prior to her appointment as Chief Executive Officer of the Company, Dr. Birx resigned as a member of the Board of Directors of Innoviva, Inc., the Company's largest shareholder, a position she assumed in March 2021. Dr. Birx served as the response coordinator of the White House Coronavirus Task Force, where she made recommendations to the vice president using data integration to drive decision making, as well as worked closely with state officials across the country to provide state specific advice and guidance. In 2014, Dr. Birx became an Ambassador at Large, when she assumed the role of the Coordinator of the United States Government Activities to Combat HIV/AIDS and U.S. Special Representative for Global Health Diplomacy (a $6 billion per year program), a position she served in until January 2021. As the U.S. Global AIDS Coordinator, Dr. Birx oversaw the President's Emergency Plan for AIDS Relief (PEPFAR), the largest commitment by any nation to combat a single disease in history, at the CDC as well as all U.S. Government engagement with the Global Fund to Fight AIDS, Tuberculosis and Malaria. From 2005 until 2014, Dr. Birx served successfully as the Director of CDC's Division of Global HIV/AIDS (DGHA) in the CDC Center for Global Health where she developed ISO and CAP certified laboratories across the globe. From 1996 until 2005, she served as the Director of the U.S. Military HIV Research Program (USMHRP) at the Walter Reed Army Institute of Research directing research and development of HIV vaccines through full Phase III trials, including GLP and GMP manufacturing. During this time, she also rose to the rank of Colonel. Then known as Colonel Birx, she was awarded three prestigious U.S. Meritorious Service Medals and the Legion of Merit Award for her groundbreaking research, leadership and management skills during her tenure at the Department of Defense (DoD). In 1985, Dr. Birx began her career with the DoD as a military trained clinician in cellular immunology, focusing on HIV/AIDS vaccine research. Dr. Birx has published over 230 manuscripts in peer reviewed journals, authored nearly a dozen chapters in scientific publications, as well as developed and patented vaccines. Dr. Birx currently serves as a member of the Board of Directors of Nanolive SA.Dr. Birx received her medical degree from the Hershey School of Medicine, Pennsylvania State University in 1980 and her B.S. from Houghton College in 1976. Dr. Birx is board certified in internal medicine, allergy and immunology, and diagnostic and clinical laboratory immunology. Dr. Birx is a world renowned medical expert and leader whose long career has focused on clinical and basic immunology, infectious diseases, pandemic preparedness, vaccine research, and global health.- Deborah L. Birx自2023年7月起担任Armata Pharmaceuticals, Inc.的首席执行官。在被任命为公司首席执行官之前,Birx博士于2021年3月辞去了公司最大股东Innoviva, Inc.的董事会成员职务。Birx博士曾担任白宫冠状病毒特别工作组的应对协调员,在那里她向副总统提出建议,利用数据整合来推动决策,并与全国各地的州官员密切合作,提供具体的州建议和指导。2014年,伯克斯博士成为一名在逃大使,当时她担任美国政府抗击艾滋病毒/艾滋病活动协调员和美国全球卫生外交特别代表(每年60亿美元的项目),她在该职位任职至2021年1月。作为美国全球艾滋病协调员,伯克斯博士在疾病预防控制中心监督总统的艾滋病紧急救援计划(PEPFAR),这是历史上任何国家对抗单一疾病的最大承诺,以及美国政府与全球抗击艾滋病、结核病和疟疾基金的所有接触。从2005年到2014年,Birx博士在CDC全球健康中心成功担任CDC全球艾滋病毒/艾滋病(DGHA)司司长,在那里她在全球开发了ISO和CAP认证实验室。从1996年到2005年,她在沃尔特里德陆军研究所担任美国军事HIV研究项目(USMHRP)主任,指导HIV疫苗的研发通过完整的III期试验,包括GLP和GMP制造。在这段时间里,她也升到了上校军衔。当时被称为Birx上校的她在国防部(DOD)任职期间凭借开创性的研究、领导和管理技能,获得了三项享有盛誉的美国立功奖章和军团功勋奖。1985年,Birx博士开始了她在国防部的职业生涯,成为一名受过军事训练的细胞免疫学临床医生,专注于HIV/AIDS疫苗研究。Birx博士在同行评审的期刊上发表了230多篇稿件,在科学出版物中撰写了近十几个章节,还开发了疫苗和专利疫苗。Birx博士目前担任Nanolive SA.Dr董事会成员。伯克斯于1980年获得宾夕法尼亚州立大学赫尔希医学院的医学学位,并于1976年获得霍顿学院的学士学位。Birx博士在内科、过敏和免疫学以及诊断和临床实验室免疫学方面获得董事会认证。Birx博士是世界著名的医学专家和领导者,其长期职业生涯专注于临床和基础免疫学、传染病、大流行防范、疫苗研究和全球健康。
- Deborah L. Birx has served as Armata Pharmaceuticals, Inc.'s Chief Executive Officer since July 2023. Prior to her appointment as Chief Executive Officer of the Company, Dr. Birx resigned as a member of the Board of Directors of Innoviva, Inc., the Company's largest shareholder, a position she assumed in March 2021. Dr. Birx served as the response coordinator of the White House Coronavirus Task Force, where she made recommendations to the vice president using data integration to drive decision making, as well as worked closely with state officials across the country to provide state specific advice and guidance. In 2014, Dr. Birx became an Ambassador at Large, when she assumed the role of the Coordinator of the United States Government Activities to Combat HIV/AIDS and U.S. Special Representative for Global Health Diplomacy (a $6 billion per year program), a position she served in until January 2021. As the U.S. Global AIDS Coordinator, Dr. Birx oversaw the President's Emergency Plan for AIDS Relief (PEPFAR), the largest commitment by any nation to combat a single disease in history, at the CDC as well as all U.S. Government engagement with the Global Fund to Fight AIDS, Tuberculosis and Malaria. From 2005 until 2014, Dr. Birx served successfully as the Director of CDC's Division of Global HIV/AIDS (DGHA) in the CDC Center for Global Health where she developed ISO and CAP certified laboratories across the globe. From 1996 until 2005, she served as the Director of the U.S. Military HIV Research Program (USMHRP) at the Walter Reed Army Institute of Research directing research and development of HIV vaccines through full Phase III trials, including GLP and GMP manufacturing. During this time, she also rose to the rank of Colonel. Then known as Colonel Birx, she was awarded three prestigious U.S. Meritorious Service Medals and the Legion of Merit Award for her groundbreaking research, leadership and management skills during her tenure at the Department of Defense (DoD). In 1985, Dr. Birx began her career with the DoD as a military trained clinician in cellular immunology, focusing on HIV/AIDS vaccine research. Dr. Birx has published over 230 manuscripts in peer reviewed journals, authored nearly a dozen chapters in scientific publications, as well as developed and patented vaccines. Dr. Birx currently serves as a member of the Board of Directors of Nanolive SA.Dr. Birx received her medical degree from the Hershey School of Medicine, Pennsylvania State University in 1980 and her B.S. from Houghton College in 1976. Dr. Birx is board certified in internal medicine, allergy and immunology, and diagnostic and clinical laboratory immunology. Dr. Birx is a world renowned medical expert and leader whose long career has focused on clinical and basic immunology, infectious diseases, pandemic preparedness, vaccine research, and global health.
- David D. House
David D. House自2024年8月起担任Armata Pharmaceuticals, Inc.高级副总裁、财务和首席财务官。在加入公司之前,House先生曾于2018年10月至2024年5月在多渠道医师配发护肤品公司ZO Skin Health,Inc.担任公司财务总监和会计副总裁。在ZO皮肤健康,他领导了全球会计业务,管理财务报告,并在该公司被黑石收购的过程中发挥了关键作用。他还成立了国际子公司,并监督并购的财务整合。House先生的经验包括在临床阶段生物制药公司Peregrine Pharmaceuticals,Inc.和Avid Bioservices, Inc.(CDMO)担任类似的财务领导职务,他在一家合同开发和制造组织担任财务总监,负责实施ASC 606、管理技术会计以及进行SEC报告。他的职业生涯还包括在Viant,Inc.(DSP)、Sourcing Solutions,LLC和Apria Healthcare(APR)担任职务,在那里他担任过多个会计和财务管理职位。在其职业生涯的早期阶段,豪斯曾在公共会计师事务所Windes担任高级审计员。在那里,他管理着针对公共、私人和非盈利实体的全面审计,并为SEC文件和内部控制评估做出了贡献。豪斯拥有加州州立大学富勒顿分校会计专业的工商管理文学学士学位。他于2011年1月5日获得加州注册会计师执照,目前处于非活动状态。
David D. House has served as Armata Pharmaceuticals, Inc.'s Senior Vice President, Finance and Principal Financial Officer since August 2024. Before joining the Company, Mr. House, served as Corporate Controller and Vice President of Accounting at ZO Skin Health, Inc., a multi channel physician dispensed skincare company, from October 2018 to May 2024. At ZO Skin Health, he led global accounting operations, managed financial reporting, and played a crucial role in the company's acquisition by Blackstone. He also established international subsidiaries and oversaw financial integration for mergers and acquisitions. Mr. House's experience includes similar financial leadership roles at Peregrine Pharmaceuticals, Inc., a clinical stage biopharmaceutical company, and Avid Bioservices, Inc. (CDMO), a contract development and manufacturing organization where he served as Controller and was responsible for implementing ASC 606, managing technical accounting, and conducting SEC reporting. His career also includes roles at Viant, Inc. (DSP), Sourcing Solutions, LLC, and Apria Healthcare (APR), where he held various accounting and financial management positions. In the early stages of his career, Mr. House worked as a Senior Auditor at Windes, a public accounting firm. There, he managed comprehensive audits for public, private, and not for profit entities and contributed to SEC filings and internal control evaluations.Mr. House holds a Bachelor of Arts in Business Administration with an Accounting concentration from California State University, Fullerton. He obtained his California CPA license on January 5, 2011, which is currently inactive.- David D. House自2024年8月起担任Armata Pharmaceuticals, Inc.高级副总裁、财务和首席财务官。在加入公司之前,House先生曾于2018年10月至2024年5月在多渠道医师配发护肤品公司ZO Skin Health,Inc.担任公司财务总监和会计副总裁。在ZO皮肤健康,他领导了全球会计业务,管理财务报告,并在该公司被黑石收购的过程中发挥了关键作用。他还成立了国际子公司,并监督并购的财务整合。House先生的经验包括在临床阶段生物制药公司Peregrine Pharmaceuticals,Inc.和Avid Bioservices, Inc.(CDMO)担任类似的财务领导职务,他在一家合同开发和制造组织担任财务总监,负责实施ASC 606、管理技术会计以及进行SEC报告。他的职业生涯还包括在Viant,Inc.(DSP)、Sourcing Solutions,LLC和Apria Healthcare(APR)担任职务,在那里他担任过多个会计和财务管理职位。在其职业生涯的早期阶段,豪斯曾在公共会计师事务所Windes担任高级审计员。在那里,他管理着针对公共、私人和非盈利实体的全面审计,并为SEC文件和内部控制评估做出了贡献。豪斯拥有加州州立大学富勒顿分校会计专业的工商管理文学学士学位。他于2011年1月5日获得加州注册会计师执照,目前处于非活动状态。
- David D. House has served as Armata Pharmaceuticals, Inc.'s Senior Vice President, Finance and Principal Financial Officer since August 2024. Before joining the Company, Mr. House, served as Corporate Controller and Vice President of Accounting at ZO Skin Health, Inc., a multi channel physician dispensed skincare company, from October 2018 to May 2024. At ZO Skin Health, he led global accounting operations, managed financial reporting, and played a crucial role in the company's acquisition by Blackstone. He also established international subsidiaries and oversaw financial integration for mergers and acquisitions. Mr. House's experience includes similar financial leadership roles at Peregrine Pharmaceuticals, Inc., a clinical stage biopharmaceutical company, and Avid Bioservices, Inc. (CDMO), a contract development and manufacturing organization where he served as Controller and was responsible for implementing ASC 606, managing technical accounting, and conducting SEC reporting. His career also includes roles at Viant, Inc. (DSP), Sourcing Solutions, LLC, and Apria Healthcare (APR), where he held various accounting and financial management positions. In the early stages of his career, Mr. House worked as a Senior Auditor at Windes, a public accounting firm. There, he managed comprehensive audits for public, private, and not for profit entities and contributed to SEC filings and internal control evaluations.Mr. House holds a Bachelor of Arts in Business Administration with an Accounting concentration from California State University, Fullerton. He obtained his California CPA license on January 5, 2011, which is currently inactive.
- Pierre Kyme
Pierre Kyme于2024年6月被任命为Armata的首席商务官。Kyme博士目前还担任Armata澳大利亚子公司的董事会成员。Kyme博士致力于Armata的商业和企业发展活动,这一角色始于2015年的C3J Therapeutics。此前,Kyme博士从2012年起担任C3J Therapeutics的首席科学家和产品开发总监,领导一个团队制定战略并交付关键数据,这些数据对于推进一种领先的抗菌分子通过2期人体临床试验至关重要。他还为该公司的管道项目做出了贡献,提供了医疗和商业理由来证明管道扩张的合理性。在加入Armata之前,Kyme博士花了五年时间在Cedars Sinai医疗中心成熟他的药物开发生涯,领导项目团队从概念到传染病和免疫学的临床前研究。他以这一身份与技术转让办公室密切合作,是马拉尼亚克卓越研究奖的获得者。在此之前,Kyme博士与Qiagen Pty. Ltd.合作,在悉尼千年研究所工作,作为国家优先拨款的一部分,用于紧急研究禽流感。Kyme博士还曾担任精品投资银行Cappello Global的澳大利亚服务台和生命科学与医疗保健实践的科学顾问,并担任一家全球专业生命科学投资公司的顾问分析师,评估多个治疗领域。他的工作为美国一家私营肿瘤生物技术公司筹集了6000万美元的资金,该公司于2012年启动了世界上最大的黑色素瘤疫苗3期人体临床试验。Kyme博士在澳大利亚悉尼大学获得医学博士学位,其中大部分是作为德国蒂宾根大学的特邀学者完成的。他在加拿大温哥华的Michael Smith实验室完成了博士后培训,在盖茨基金会全球健康大挑战倡议的800万美元资助下,与Inimex Pharmaceuticals(已被Soligenix收购)合作开发先天防御调节器。
Pierre Kyme was appointed Chief Business Officer of Armata in June 2024. Dr. Kyme also currently serves as a member of the boards of directors of Armata's Australian subsidiaries. Dr. Kyme is devoted to Armata's business and corporate development activities, a role that started at C3J Therapeutics in 2015. Previously, Dr. Kyme served as a lead Scientist and Director of Product Development at C3J Therapeutics from 2012, leading a team that set strategy and delivered key data essential for advancing a lead antimicrobial molecule through Phase 2 human clinical trials. He also contributed to the company's pipeline programs, providing medical and commercial rationale to justify pipeline expansion. Prior to joining Armata, Dr. Kyme spent five years maturing his drug development career at Cedars Sinai Medical Center leading project teams from concept through preclinical research in infectious disease and immunology. In this capacity, he worked closely with the Technology Transfer Office, and was the recipient of the Malaniak Award for Excellence in Research. Prior to this, in partnership with Qiagen Pty. Ltd., Dr. Kyme worked at Sydney's Millennium Institute, as part of a priority national grant for urgent research into avian influenza. Dr. Kyme has also served as Scientific Advisor for the Australia Desk and Life Sciences & Healthcare Practice at Cappello Global, a boutique investment bank, and as consultant analyst to a global specialist life sciences investment firm, evaluating multiple therapeutic areas. His work contributed to a $60 million capital raising for a private U.S. oncology biotech, which in 2012 initiated the world's largest Phase 3 human clinical trial for a melanoma vaccine. Dr. Kyme earned his Ph.D. in Medicine from the University of Sydney, Australia, the bulk of which was accomplished as an invited scholar at the University of Tübingen, Germany. He completed his postdoctoral training at the Michael Smith Laboratories in Vancouver, Canada, under an $8 million grant from the Gates Foundation Grand Challenges in Global Health initiative, developing Innate Defense Regulators in partnership with Inimex Pharmaceuticals (acquired by Soligenix).- Pierre Kyme于2024年6月被任命为Armata的首席商务官。Kyme博士目前还担任Armata澳大利亚子公司的董事会成员。Kyme博士致力于Armata的商业和企业发展活动,这一角色始于2015年的C3J Therapeutics。此前,Kyme博士从2012年起担任C3J Therapeutics的首席科学家和产品开发总监,领导一个团队制定战略并交付关键数据,这些数据对于推进一种领先的抗菌分子通过2期人体临床试验至关重要。他还为该公司的管道项目做出了贡献,提供了医疗和商业理由来证明管道扩张的合理性。在加入Armata之前,Kyme博士花了五年时间在Cedars Sinai医疗中心成熟他的药物开发生涯,领导项目团队从概念到传染病和免疫学的临床前研究。他以这一身份与技术转让办公室密切合作,是马拉尼亚克卓越研究奖的获得者。在此之前,Kyme博士与Qiagen Pty. Ltd.合作,在悉尼千年研究所工作,作为国家优先拨款的一部分,用于紧急研究禽流感。Kyme博士还曾担任精品投资银行Cappello Global的澳大利亚服务台和生命科学与医疗保健实践的科学顾问,并担任一家全球专业生命科学投资公司的顾问分析师,评估多个治疗领域。他的工作为美国一家私营肿瘤生物技术公司筹集了6000万美元的资金,该公司于2012年启动了世界上最大的黑色素瘤疫苗3期人体临床试验。Kyme博士在澳大利亚悉尼大学获得医学博士学位,其中大部分是作为德国蒂宾根大学的特邀学者完成的。他在加拿大温哥华的Michael Smith实验室完成了博士后培训,在盖茨基金会全球健康大挑战倡议的800万美元资助下,与Inimex Pharmaceuticals(已被Soligenix收购)合作开发先天防御调节器。
- Pierre Kyme was appointed Chief Business Officer of Armata in June 2024. Dr. Kyme also currently serves as a member of the boards of directors of Armata's Australian subsidiaries. Dr. Kyme is devoted to Armata's business and corporate development activities, a role that started at C3J Therapeutics in 2015. Previously, Dr. Kyme served as a lead Scientist and Director of Product Development at C3J Therapeutics from 2012, leading a team that set strategy and delivered key data essential for advancing a lead antimicrobial molecule through Phase 2 human clinical trials. He also contributed to the company's pipeline programs, providing medical and commercial rationale to justify pipeline expansion. Prior to joining Armata, Dr. Kyme spent five years maturing his drug development career at Cedars Sinai Medical Center leading project teams from concept through preclinical research in infectious disease and immunology. In this capacity, he worked closely with the Technology Transfer Office, and was the recipient of the Malaniak Award for Excellence in Research. Prior to this, in partnership with Qiagen Pty. Ltd., Dr. Kyme worked at Sydney's Millennium Institute, as part of a priority national grant for urgent research into avian influenza. Dr. Kyme has also served as Scientific Advisor for the Australia Desk and Life Sciences & Healthcare Practice at Cappello Global, a boutique investment bank, and as consultant analyst to a global specialist life sciences investment firm, evaluating multiple therapeutic areas. His work contributed to a $60 million capital raising for a private U.S. oncology biotech, which in 2012 initiated the world's largest Phase 3 human clinical trial for a melanoma vaccine. Dr. Kyme earned his Ph.D. in Medicine from the University of Sydney, Australia, the bulk of which was accomplished as an invited scholar at the University of Tübingen, Germany. He completed his postdoctoral training at the Michael Smith Laboratories in Vancouver, Canada, under an $8 million grant from the Gates Foundation Grand Challenges in Global Health initiative, developing Innate Defense Regulators in partnership with Inimex Pharmaceuticals (acquired by Soligenix).