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Arvinas Appoints Paul McInulty as Senior Vice President, Regulatory Affairs
Arvinas Appoints Paul McInulty as Senior Vice President, Regulatory Affairs
NEW HAVEN, Conn., Oct. 03, 2022 (GLOBE NEWSWIRE) -- Arvinas, Inc. (Nasdaq: ARVN), a clinical-stage biotechnology company creating a new class of drugs based on targeted protein degradation, today announced that Paul McInulty has joined the company as Senior Vice President, Regulatory Affairs.
"We are delighted to welcome Paul to our leadership team in this crucial role as we enter the next phase of Arvinas – a late-stage development company," said John Houston, Ph.D., Arvinas President and Chief Executive Officer. "Paul's vast experience leading global and regional development programs from discovery through commercialization in a wide range of therapeutic areas and modalities will be very valuable as Arvinas continues on an incredible growth trajectory."
Mr. McInulty brings more than 25 years of biopharmaceutical experience to Arvinas. He recently served as Vice President, Therapeutic Head, Hematology and Precision Medicines Regulatory Affairs at Bristol Myers Squibb and spent just over 15 years at Celgene Corporation in various roles of increasing responsibility including serving as Vice President, Regulatory Affairs, Hematology and Oncology.
"I am excited to join Arvinas and to be part of the company that is truly leading the way in the targeted protein degradation industry through its validated PROTAC® protein degradation platform," said Mr. McInulty. "As Arvinas transitions into a late-stage development company, I look forward to supporting the organization on this journey and the opportunity to contribute my experience in leading global regulatory strategies."
About Arvinas
Arvinas is a clinical-stage biotechnology company dedicated to improving the lives of patients suffering from debilitating and life-threatening diseases through the discovery, development, and commercialization of therapies that degrade disease-causing proteins. Arvinas uses its proprietary PROTAC® Discovery Engine platform to engineer proteolysis targeting chimeras, or PROTAC® targeted protein degraders, that are designed to harness the body's own natural protein disposal system to selectively and efficiently degrade and remove disease-causing proteins. In addition to its robust preclinical pipeline of PROTAC® protein degraders against validated and "undruggable" targets, the company has three investigational clinical-stage programs: bavdegalutamide and ARV-766 for the treatment of men with metastatic castration-resistant prostate cancer; and ARV-471 for the treatment of patients with locally advanced or metastatic ER+/HER2- breast cancer. For more information, visit .
Forward-Looking Statements
This press release contains forward-looking statements that involve substantial risks and uncertainties, including statements regarding the potential advantages and therapeutic benefits of our product candidates, the future development and potential marketing approval and commercialization of our product candidates, including the initiation of and timing of data from our clinical trials. All statements, other than statements of historical facts, contained in this press release, including statements regarding our strategy, future operations, prospects, plans and objectives of management, are forward-looking statements. The words "anticipate," "believe," "estimate," "expect," "intend," "may," "might," "plan," "predict," "project," "target," "potential," "will," "would," "could," "should," "continue," and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words.
We may not actually achieve the plans, intentions or expectations disclosed in our forward-looking statements, and you should not place undue reliance on our forward-looking statements. Actual results or events could differ materially from the plans, intentions and expectations disclosed in the forward-looking statements we make as a result of various risks and uncertainties, including but not limited to:, whether we will be able to successfully conduct and complete clinical development of our product candidates, including whether we initiate and receive results from our clinical trials on our expected timelines or at all, obtain marketing approval for and commercialize our product candidates on our current timelines or at all and other important factors discussed in the "Risk Factors" sections contained in our quarterly and annual reports on file with the Securities and Exchange Commission. The forward-looking statements contained in this press release reflect our current views with respect to future events, and we assume no obligation to update any forward-looking statements except as required by applicable law. These forward-looking statements should not be relied upon as representing our views as of any date subsequent to the date of this release.
Contacts
Investors:
Jeff Boyle
347-247-5089
Jeff.Boyle@arvinas.com
Media:
Kirsten Owens
203-584-0307
Kirsten.Owens@arvinas.com
NEW HAVEN, Conn., Oct. 03, 2022 (GLOBE NEWSWIRE) -- Arvinas, Inc. (Nasdaq: ARVN), a clinical-stage biotechnology company creating a new class of drugs based on targeted protein degradation, today announced that Paul McInulty has joined the company as Senior Vice President, Regulatory Affairs.
康涅狄格州纽黑文,2022年10月3日(环球网)--阿维纳斯公司(纳斯达克:ARVN),一家临床阶段的生物技术公司,创造了一种基于靶向蛋白质降解的新型药物,今天宣布保罗·麦克纳尔蒂加盟该公司,担任监管事务高级副总裁。
"We are delighted to welcome Paul to our leadership team in this crucial role as we enter the next phase of Arvinas – a late-stage development company," said John Houston, Ph.D., Arvinas President and Chief Executive Officer. "Paul's vast experience leading global and regional development programs from discovery through commercialization in a wide range of therapeutic areas and modalities will be very valuable as Arvinas continues on an incredible growth trajectory."
Mr. McInulty brings more than 25 years of biopharmaceutical experience to Arvinas. He recently served as Vice President, Therapeutic Head, Hematology and Precision Medicines Regulatory Affairs at Bristol Myers Squibb and spent just over 15 years at Celgene Corporation in various roles of increasing responsibility including serving as Vice President, Regulatory Affairs, Hematology and Oncology.
阿维纳斯公司首席执行官兼首席执行官约翰·休斯顿博士说:“在我们进入阿维纳斯公司的下一阶段之际,我们很高兴欢迎保罗加入我们的领导团队,担任这一至关重要的角色。随着阿维纳斯公司继续在令人难以置信的增长轨道上前进,保罗领导全球和地区发展计划的丰富经验将非常宝贵,从发现到在广泛的治疗领域和方式进行商业化。“
麦克纳蒂先生为阿维纳斯公司带来了超过25年的生物制药经验。他最近担任百时美施贵宝治疗、血液和精密药物监管事务副主任总裁,并在Celgene Corporation工作了15年多,担任过各种职责,包括担任总裁副主任、监管事务、血液和肿瘤科。
"I am excited to join Arvinas and to be part of the company that is truly leading the way in the targeted protein degradation industry through its validated PROTAC® protein degradation platform," said Mr. McInulty. "As Arvinas transitions into a late-stage development company, I look forward to supporting the organization on this journey and the opportunity to contribute my experience in leading global regulatory strategies."
我很高兴能加入阿维纳斯,成为这家通过其经过验证的PROTAC在目标蛋白质降解行业中真正领先的公司的一员®随着Arvinas过渡到一家后期开发公司,我期待着在这段旅程中支持该组织,并有机会在领先的全球监管战略方面贡献我的经验。
About Arvinas
Arvinas is a clinical-stage biotechnology company dedicated to improving the lives of patients suffering from debilitating and life-threatening diseases through the discovery, development, and commercialization of therapies that degrade disease-causing proteins. Arvinas uses its proprietary PROTAC® Discovery Engine platform to engineer proteolysis targeting chimeras, or PROTAC® targeted protein degraders, that are designed to harness the body's own natural protein disposal system to selectively and efficiently degrade and remove disease-causing proteins. In addition to its robust preclinical pipeline of PROTAC® protein degraders against validated and "undruggable" targets, the company has three investigational clinical-stage programs: bavdegalutamide and ARV-766 for the treatment of men with metastatic castration-resistant prostate cancer; and ARV-471 for the treatment of patients with locally advanced or metastatic ER+/HER2- breast cancer. For more information, visit .
关于阿维纳斯
Arvinas是一家临床阶段的生物技术公司,致力于通过发现、开发和商业化降低致病蛋白的疗法来改善患有衰弱和危及生命的疾病患者的生活。Arvinas使用其专有的PROTAC®发现引擎平台,用于设计针对嵌合体的蛋白质分解,或PROTAC®靶向蛋白质降解剂,旨在利用人体自身的天然蛋白质处理系统,选择性、高效地降解和去除致病蛋白质。除了其强大的PROTAC临床前流水线®该公司有三个研究阶段的临床计划:用于治疗男性转移性去势耐受前列腺癌的巴夫地格鲁胺和ARV-766;以及用于治疗局部晚期或转移性ER+/HER2乳腺癌患者的ARV-471。有关更多信息,请访问。
Forward-Looking Statements
This press release contains forward-looking statements that involve substantial risks and uncertainties, including statements regarding the potential advantages and therapeutic benefits of our product candidates, the future development and potential marketing approval and commercialization of our product candidates, including the initiation of and timing of data from our clinical trials. All statements, other than statements of historical facts, contained in this press release, including statements regarding our strategy, future operations, prospects, plans and objectives of management, are forward-looking statements. The words "anticipate," "believe," "estimate," "expect," "intend," "may," "might," "plan," "predict," "project," "target," "potential," "will," "would," "could," "should," "continue," and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words.
前瞻性陈述
本新闻稿包含涉及重大风险和不确定性的前瞻性陈述,包括有关我们候选产品的潜在优势和治疗益处、我们候选产品的未来开发和潜在市场批准以及商业化的陈述,包括我们临床试验数据的启动和时间安排。除有关历史事实的陈述外,本新闻稿中包含的所有陈述,包括有关我们的战略、未来业务、前景、计划和管理目标的陈述,都是前瞻性陈述。“预期”、“相信”、“估计”、“预期”、“打算”、“可能”、“可能”、“计划”、“预测”、“项目”、“目标”、“潜在”、“将”、“可能”、“可能”、“应该”、“继续”以及类似的表述旨在识别前瞻性表述,尽管并不是所有前瞻性表述都包含这些识别词语。
We may not actually achieve the plans, intentions or expectations disclosed in our forward-looking statements, and you should not place undue reliance on our forward-looking statements. Actual results or events could differ materially from the plans, intentions and expectations disclosed in the forward-looking statements we make as a result of various risks and uncertainties, including but not limited to:, whether we will be able to successfully conduct and complete clinical development of our product candidates, including whether we initiate and receive results from our clinical trials on our expected timelines or at all, obtain marketing approval for and commercialize our product candidates on our current timelines or at all and other important factors discussed in the "Risk Factors" sections contained in our quarterly and annual reports on file with the Securities and Exchange Commission. The forward-looking statements contained in this press release reflect our current views with respect to future events, and we assume no obligation to update any forward-looking statements except as required by applicable law. These forward-looking statements should not be relied upon as representing our views as of any date subsequent to the date of this release.
我们可能无法实际实现我们的前瞻性声明中披露的计划、意图或预期,您不应过度依赖我们的前瞻性声明。由于各种风险和不确定性,实际结果或事件可能与我们在前瞻性声明中披露的计划、意图和预期大不相同,这些风险和不确定性包括但不限于:我们是否能够成功地对我们的候选产品进行和完成临床开发,包括我们是否能够在预期的时间表上启动我们的临床试验并收到结果,或者在我们目前的时间表上为我们的候选产品获得营销批准并将其商业化,以及在提交给美国证券交易委员会的季度和年度报告中的“风险因素”部分讨论的其他重要因素。本新闻稿中包含的前瞻性陈述反映了我们对未来事件的当前看法,除非适用法律要求,否则我们没有义务更新任何前瞻性陈述。这些前瞻性陈述不应被视为代表我们在本新闻稿发布之日之后的任何日期的观点。
Contacts
Investors:
Jeff Boyle
347-247-5089
Jeff.Boyle@arvinas.com
联系人
投资者:
Jeff·博伊尔
347-247-5089
邮箱:Jeff.Boyle@arvinas.com
Media:
Kirsten Owens
203-584-0307
Kirsten.Owens@arvinas.com
媒体:
柯尔斯滕·欧文斯
203-584-0307
邮箱:Kirst.Owens@arvinas.com
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