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NewAmsterdam Pharma Announces Appointment of William "BJ" Jones, Formerly of Biohaven Pharmaceuticals, as Chief Commercial Officer

NewAmsterdam Pharma Announces Appointment of William "BJ" Jones, Formerly of Biohaven Pharmaceuticals, as Chief Commercial Officer

NewAmsterdam Pharma 宣布任命曾在 Biohaven Pharmicals 任职 William “BJ” Jones
GlobeNewswire ·  2023/08/14 16:01

NAARDEN, The Netherlands and MIAMI, Aug. 14, 2023 (GLOBE NEWSWIRE) -- NewAmsterdam Pharma Company N.V. (Nasdaq: NAMS or "NewAmsterdam" or the "Company"), a clinical-stage biopharmaceutical company developing oral, non-statin medicines for patients at high risk of cardiovascular disease with residual elevation of low-density lipoprotein cholesterol ("LDL-C"), for whom existing therapies are not sufficiently effective or well-tolerated, today announced the appointment of William "BJ" Jones as the Company's first Chief Commercial Officer ("CCO"), effective August 14, 2023. Mr. Jones brings 30 years of commercial and launch experience in the U.S. and globally, with particular experience in driving mass market product launch strategies for industry-leading brands. At NewAmsterdam, he will build and lead all commercial functions, including marketing, market access, sales, medical science engagement and commercial operations.

荷兰纳尔登和迈阿密,2023年8月14日(环球网)--新阿姆斯特丹制药公司(纳斯达克代码:NAMS或“新阿姆斯特丹”或“公司”)是一家临床阶段的生物制药公司,为心血管疾病高风险、低密度脂蛋白胆固醇(“LDL-C”)残留升高的患者开发口服非他汀类药物,现有疗法对这些患者不够有效或耐受性不佳。该公司今天宣布任命威廉·“BJ”琼斯为公司首任首席商务官,自2023年8月14日起生效。Mr.Jones在美国和全球拥有30年的商业和产品发布经验,尤其是在推动行业领先品牌的大众市场产品发布战略方面具有丰富的经验。在新阿姆斯特丹,他将建立和领导所有商业职能,包括营销、市场准入、销售、医学科学参与和商业运营。

"We are delighted to welcome BJ to our team. With obicetrapib progressing through pivotal Phase 3 development, now is the right time to begin building a powerful commercial organization, with the potential to deliver our oral, low-dose, once-daily CETP inhibitor, if approved, to the millions of dyslipidemia patients globally in need of better options," said Dr. Michael Davidson, M.D., President & Chief Executive Officer. "BJ is an exceptional leader with a proven track record of building commercial organizations, developing strategic and creative go-to-market strategies, and launching industry-leading products in mass markets, including in the cardiovascular disease space. We believe BJ's expertise uniquely complements our existing team, and we look forward to his leadership as we mature NewAmsterdam into a fully integrated company and work to ultimately deliver on the promise of CETP inhibition to address major unmet needs across cardiometabolic diseases."

“我们很高兴欢迎BJ加入我们的团队。随着ObicetRapib在关键的3期开发中取得进展,现在是开始建立一个强大的商业组织的合适时机,如果获得批准,我们有可能向全球数百万需要更好选择的血脂异常患者提供我们的口服、低剂量、每天一次的CETP抑制剂,”医学博士、总裁和首席执行官迈克尔·戴维森博士说。BJ是一位杰出的领导者,在建立商业组织、开发战略性和创造性的上市战略以及在大众市场(包括心血管疾病领域)推出业界领先产品方面有着良好的业绩记录。我们相信BJ的专业知识是对我们现有团队的独特补充,我们期待着他的领导,随着我们将新阿姆斯特丹发展成为一家完全整合的公司,并努力最终兑现抑制CETP的承诺,以满足心脏代谢疾病方面尚未得到满足的主要需求。“

Mr. Jones joins NewAmsterdam with three decades of commercial and launch experience in both large pharmaceutical and small biotech companies. Most recently, he served as CCO, Migraine & Common Diseases at Biohaven Pharmaceuticals, which was acquired by Pfizer for $11.6B. During his tenure, Mr. Jones led the commercial enterprise that launched Biohaven's Nurtec ODT. Earlier in his career, Mr. Jones held leadership roles of increasing responsibility at Takeda Pharmaceuticals, AstraZeneca, Bristol-Myers Squibb, Boehringer Ingelheim and NitroMed, during which time he supported mass market product launches for notable brands including Excedrin Migraine, Farxiga, Pradaxa, BiDil, and Abilify. Mr. Jones is a graduate of the United Air Force Academy and attained the rank of Major through his active duty and reserve service. He holds an M.B.A from Stanford Graduate School of Business and an M.S. in Industrial Engineering from Texas A&M University.

Mr.Jones加盟新阿姆斯特丹,拥有30年的大型制药和小型生物技术公司的商业和发布经验。最近,他在生物港制药公司担任首席运营官,负责偏头痛和常见病,该公司被辉瑞以116亿美元的价格收购。在任职期间,Mr.Jones领导的商业企业推出了生物港的Nurtec奥特。在他职业生涯的早期,Mr.Jones在武田制药、阿斯利康、百时美施贵宝、勃林格-英格尔海姆和硝化甘油担任领导职务,在此期间,他支持包括Excedrin Migraine在内的知名品牌的大众市场产品发布,Farxiga,普拉达萨,BiDil、和Abilify。Mr.Jones毕业于联合空军学院,通过现役和预备役获得少校军衔。他拥有斯坦福大学商学院的工商管理硕士学位和德克萨斯农工大学的工业工程硕士学位。

"I am excited to be a part of NewAmsterdam Pharma, a company that I believe is uniquely positioned in the quest to alleviate the impact of the world's leading cause of mortality—cardiovascular disease. Based on data reported to-date, I believe obicetrapib, if approved, has the potential to solve a substantial challenge in cardiovascular disease, helping many more patients achieve their risk-based LDL-C goals, while positively impacting a number of other lipid and lipoprotein parameters associated with cardiovascular disease risk," said Mr. Jones. "I look forward to leveraging my experience to build NewAmsterdam's commercial team and operations and to partnering with the management team to unlock obicetrapib's value as a potentially safe and effective oral therapy that could change the treatment paradigm for patients worldwide."

Mr.Jones说:“我很高兴能成为新阿姆斯特丹制药公司的一员,我相信这家公司在寻求减轻世界主要死亡原因-心血管疾病的影响方面处于独特的地位。根据迄今报告的数据,我相信如果获得批准,obicetRapib有可能解决心血管疾病方面的重大挑战,帮助更多的患者实现基于风险的低密度脂蛋白-C目标,同时对其他一些与心血管疾病风险相关的血脂和脂蛋白参数产生积极影响。”我期待着利用我的经验来建立新阿姆斯特丹的商业团队和业务,并与管理团队合作,释放obicetRapib作为一种潜在的安全有效的口服疗法的价值,这可能会改变世界各地患者的治疗模式。“

About NewAmsterdam

关于新阿姆斯特丹

Based in the Netherlands, NewAmsterdam (Nasdaq: NAMS) is a clinical-stage biopharmaceutical company whose mission is to improve patient care in populations with metabolic diseases where currently approved therapies have not been sufficiently adequate or well tolerated. We seek to fill a significant unmet need for a safe, cost-effective and convenient LDL-lowering therapy as an adjunct to statins, a class of lipid-lowering medications that are the current standard of care for high-risk CVD patients with high cholesterol. NewAmsterdam is investigating obicetrapib, an oral, low-dose and once-daily CETP inhibitor, as the preferred LDL-C lowering therapy to be used as an adjunct to maximally tolerated statin therapy for high-risk cardiovascular disease patients.

总部设在荷兰的新阿姆斯特丹公司(纳斯达克代码:NAMS)是一家临床阶段的生物制药公司,其使命是改善患有代谢性疾病的人群的患者护理,这些人群目前批准的治疗方法不够充分或耐受性不佳。我们寻求满足一个重要的未得到满足的需求,即作为他汀类药物的补充,安全、成本效益高和方便的降低低密度脂蛋白疗法,他汀类药物是一类降脂药物,目前是高风险心血管疾病高胆固醇患者的护理标准。新阿姆斯特丹正在研究ObicetRapib,一种口服、低剂量、每天一次的CETP抑制剂,作为高风险心血管疾病患者最大耐受性他汀类药物的首选降低低密度脂蛋白的辅助疗法。

Forward-Looking Statements

前瞻性陈述

Certain statements included in this document that are not historical facts are forward-looking statements for purposes of the safe harbor provisions under the United States Private Securities Litigation Reform Act of 1995. Forward-looking statements generally are accompanied by words such as "believe," "may," "will," "estimate," "continue," "anticipate," "intend," "expect," "should," "would," "plan," "predict," "potential," "seem," "seek," "future," "outlook" and similar expressions that predict or indicate future events or trends or that are not statements of historical matters. These forward-looking statements include, but are not limited to, statements regarding the Company's business and strategic plans, the Company's commercial opportunity, the therapeutic and curative potential of the Company's product candidate, the Company's clinical trials and the timing for enrolling patients, the timing and forums for announcing data, the achievement and timing of regulatory approvals, and plans for commercialization. These statements are based on various assumptions, whether or not identified in this document, and on the current expectations of the Company's management and are not predictions of actual performance. These forward-looking statements are provided for illustrative purposes only and are not intended to serve as and must not be relied on as a guarantee, an assurance, a prediction, or a definitive statement of fact or probability. Actual events and circumstances are difficult or impossible to predict and may differ from assumptions. Many actual events and circumstances are beyond the control of the Company. These forward-looking statements are subject to a number of risks and uncertainties, including changes in domestic and foreign business, market, financial, political, and legal conditions; risks related to the approval of the Company's product candidate and the timing of expected regulatory and business milestones, including potential commercialization; ability to negotiate definitive contractual arrangements with potential customers; the impact of competitive product candidates; ability to obtain sufficient supply of materials; global economic and political conditions, including the Russia-Ukraine conflict; the effects of competition on the Company's future business; and those factors described in the Company's public filings with the Securities Exchange Commission. Additional risks related to the Company's business include, but are not limited to: uncertainty regarding outcomes of the Company's ongoing clinical trials, particularly as they relate to regulatory review and potential approval for its product candidate; risks associated with the Company's efforts to commercialize a product candidate; the Company's ability to negotiate and enter into definitive agreements on favorable terms, if at all; the impact of competing product candidates on the Company's business; intellectual property related claims; the Company's ability to attract and retain qualified personnel; ability to continue to source the raw materials for its product candidate. If any of these risks materialize or the Company's assumptions prove incorrect, actual results could differ materially from the results implied by these forward-looking statements. There may be additional risks that the Company does not presently know or that the Company currently believes are immaterial that could also cause actual results to differ from those contained in the forward-looking statements. In addition, forward-looking statements reflect the Company's expectations, plans, or forecasts of future events and views as of the date of this document and are qualified in their entirety by reference to the cautionary statements herein. The Company anticipates that subsequent events and developments may cause the Company's assessments to change. These forward-looking statements should not be relied upon as representing the Company's assessment as of any date subsequent to the date of this communication. Accordingly, undue reliance should not be placed upon the forward-looking statements. Neither the Company nor any of its affiliates undertakes any obligation to update these forward-looking statements, except as may be required by law.

本文件中包含的非历史事实的某些陈述是为了1995年美国私人证券诉讼改革法中的安全港条款的目的而作出的前瞻性陈述。前瞻性陈述通常伴随着“相信”、“可能”、“将会”、“估计”、“继续”、“预期”、“打算”、“预期”、“应该”、“将会”、“计划”、“预测”、“潜在”、“似乎”、“寻求”、“未来”、“展望”等词汇,以及预测或表明未来事件或趋势或不是历史事件的类似表述。这些前瞻性陈述包括但不限于以下陈述:公司的业务和战略计划、公司的商业机会、公司候选产品的治疗和治疗潜力、公司的临床试验和招募患者的时机、宣布数据的时机和论坛、监管部门批准的成就和时机以及商业化计划。这些陈述基于各种假设,无论是否在本文件中确定,并基于公司管理层目前的预期,而不是对实际业绩的预测。这些前瞻性陈述仅用于说明目的,不打算也不能作为对事实或可能性的保证、保证、预测或确定性陈述。实际事件和情况很难或不可能预测,可能与假设不同。许多实际事件和情况都不是本公司所能控制的。这些前瞻性陈述会受到许多风险和不确定因素的影响,包括国内外商业、市场、金融、政治和法律条件的变化;与公司候选产品的批准和预期的监管和业务里程碑的时间相关的风险,包括潜在的商业化;与潜在客户谈判最终合同安排的能力;候选竞争产品的影响;获得充足材料的能力;全球经济和政治状况,包括俄罗斯和乌克兰的冲突;竞争对公司未来业务的影响;以及公司向证券交易委员会提交的公开文件中描述的那些因素。与公司业务相关的其他风险包括但不限于:公司正在进行的临床试验结果的不确定性,特别是与监管审查和对其候选产品的潜在批准有关的不确定性;与公司将候选产品商业化的努力相关的风险;公司以有利条件谈判并达成最终协议的能力(如果有的话);竞争产品候选产品对公司业务的影响;与知识产权相关的索赔;公司吸引和保留合格人员的能力;继续为其候选产品采购原材料的能力。如果这些风险中的任何一个成为现实,或者公司的假设被证明是不正确的,实际结果可能与这些前瞻性陈述中暗示的结果大不相同。可能存在公司目前不知道的或公司目前认为不重要的其他风险,这些风险也可能导致实际结果与前瞻性陈述中包含的结果不同。此外,前瞻性表述反映了截至本文件发表之日公司对未来事件和观点的预期、计划或预测,其全部内容均参考本文中的警告性表述予以保留。公司预计随后发生的事件和发展可能会导致公司的评估发生变化。这些前瞻性陈述不应被视为代表公司在本通讯日期之后的任何日期的评估。因此,不应过分依赖前瞻性陈述。除法律要求外,公司或其任何关联公司均不承担更新这些前瞻性陈述的义务。

Company Contact

公司联系人

Matthew Philippe
matthew.philippe@newamsterdampharma.com

马修·菲利普
邮箱:matthew.philippe@newamsterDampharma.com

Media Contact

媒体联系人

Spectrum Science on behalf of NewAmsterdam
Jenn Gordon
P: 1-202-957-7795
jgordon@spectrumscience.com

代表新阿姆斯特丹的光谱科学
珍妮·戈登
电话:1-202-957-7795
邮箱:jgordon@spectrumcerence.com

Investor Contact

投资者联系方式

Stern Investor Relations on behalf of NewAmsterdam
Hannah Deresiewicz
P: 1 212-362-1200
hannah.deresiewicz@sternir.com

代表新阿姆斯特丹的斯特恩投资者关系
汉娜·德雷谢维奇
电话:1212-362-1200
邮箱:hannah.deresiewicz@sternir.com


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