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Y-mAbs Appoints Seasoned Biopharma Executive Peter Pfreundschuh as Chief Financial Officer

Y-mAbs Appoints Seasoned Biopharma Executive Peter Pfreundschuh as Chief Financial Officer

Y-mAbs任命经验丰富的生物制药高管Peter Pfreundschuh为致富金融(临时代码)。
Y-mAbs Therapeutics ·  07/01 00:00

NEW YORK, July 01, 2024 (GLOBE NEWSWIRE) -- Y-mAbs Therapeutics, Inc. (the "Company" or "Y-mAbs") (Nasdaq: YMAB), a commercial-stage biopharmaceutical company focused on the development and commercialization of novel radioimmunotherapy and antibody-based therapeutic products for the treatment of cancer, today announced the appointment of Peter Pfreundschuh as Chief Financial Officer, effective June 28, 2024. Mr. Pfreundschuh will report to Mike Rossi, President and Chief Executive Officer.

2024年7月1日,纽约(GLOBE NEWSWIRE)——Y-mAbs Therapeutics,Inc.(以下简称“公司”或“Y-mAbs”)(纳斯达克股票代码:YMAB)是一家面向医疗、公共卫生领域的商业化生物制药公司,致力于开发和商业化新型放射免疫治疗和抗体类治疗产品,用于治疗癌症。今天宣布,彼得·普福伦奇(Peter Pfreundschuh)已于2024年6月28日正式担任首席财务官。普福伦奇将向总裁兼首席执行官迈克·罗西(Mike Rossi)汇报。

"Y-mAbs is at a critical inflection point as we continue to gain U.S. commercial traction with DANYELZA while simultaneously advancing the development of our differentiated Self-Assembly DisAssembly Pretargeted Radioimmunotherapy, or SADA-PRIT, technology platform," said Mr. Rossi. "With Peter on board as our new U.S.-based Chief Financial Officer, we believe we are in a strong position to make strategic decisions that will serve our mission of improving the lives of patients with cancer and other serious diseases. Peter brings a wealth of leadership experience across the healthcare sector with deep experience in developing and commercializing novel pharmaceutical products, and we are excited to welcome him to our team."

罗西先生表示:“在我们继续拓展DANYELZA在美国的商业推广的同时,不断推进我们不同寻常的自组装-自解组放射免疫治疗技术平台(SADA-PRIT)的开发时,Y-mAbs正处于承受关键点。”他说:“有了彼得作为我们新的美国首席财务官,我们相信我们已经处于强有力的位置,能够做出战略决策,服务于我们改善癌症和其他重大疾病患者生活的使命。彼得在医疗保健领域拥有丰富的领导经验,在开发和商业化新型药物方面经验丰富,我们很高兴迎接他加入我们的团队。”普福伦奇曾担任旅行者生物技术公司的首席财务官。在这之前,普福伦奇先生还担任过Frequency Therapeutics公司的首席财务官、业务拓展负责人,以及UroGen Pharma Ltd的首席财务官、首席合规官和公司秘书。他还曾在Sucampo Pharmaceuticals, Inc、Immunomedics, Inc和Circulite, Inc等公司担任高管职务。早期工作阶段,普福伦奇在弗吉尼亚联合会(Ernst & Young)工作,成为一名审计师。普福伦奇现任NorthStar Medical Technologies, LLC的董事会成员,NorthStar Medical Radioisotopes, LLC的母公司。他毕业于罗格斯大学商学院,获会计学学士学位,并获得莱德大学工商管理硕士学位。普福伦奇先生是新泽西州的注册会计师。

Mr. Pfreundschuh previously served as Chief Financial Officer at Voyager Therapeutics, Inc. Prior to Voyager, Mr. Pfreundschuh served as Chief Financial Officer, Head of Business Development at Frequency Therapeutics, Inc., and before that, he served as Chief Financial Officer, Chief Compliance Officer and Corporate Secretary at UroGen Pharma Ltd. He also served in executive roles at Sucampo Pharmaceuticals, Inc.Immunomedics, Inc. and Circulite, Inc. Earlier, Mr. Pfreundschuh held progressively senior roles across Finance, Commercial Operations, and Business Development at Johnson & Johnson and AstraZeneca. He began his career as an auditor at Ernst & Young, LLP. Mr. Pfreundschuh currently serves on the Board of Directors of NorthStar Medical Technologies, LLC, the parent company of NorthStar Medical Radioisotopes, LLC. He graduated from Rutgers University School of Business with a Bachelor of Science in Accounting and earned a Master of Business Administration from Rider University. Mr. Pfreundschuh is a Certified Public Accountant in the State of New Jersey.

普福伦奇先生表示:“在我们继续拓展DANYELZA在美国的商业化的同时,不断推进我们不同寻常的自组装-自解组放射免疫治疗技术平台(SADA-PRIT)的开发时,Y-mAbs正处于建立自己的强大财务基础的关键时期。” 他说:“DANYELZA在全球范围内不断拓展,凭借稳步增长的商业成功,我相信Y-mAbs有能力进一步推进我们的SADA-PRIT技术平台,并对我们思考和使用放射性药物治疗方案以改善患者生活方式做出实质性的改变。我期待与执行领导团队以及全体同事紧密合作,继续在Y-mAbs取得更大的成功。”

"I am thrilled to join the Y-mAbs team during this pivotal time for the company," said Mr. Pfreundschuh. "With a solid financial foundation fueled by the growing commercial success of DANYELZA on a global scale, I believe Y-mAbs is well positioned to further advance our SADA-PRIT technology platform and materially change the way we think about and use radiopharmaceutical therapies to improve patient lives. I look forward to working closely with the executive leadership team and others across the organization as we continue to build upon the great success at Y-mAbs."

普福伦奇先生将在Y-mAbs位于纽约和新泽西的办事处工作。Y-mAbs是一家面向医疗、公共卫生领域的商业化生物制药公司,致力于开发和商业化新式放射性免疫治疗和抗体类治疗癌症产品。公司技术包括其自行组装 - 自行拆卸("SADA")靶向放射免疫治疗平台("PRIT")和利用Y-BiClone平台生成的双特异性抗体。公司的产品线包括抗GD2疗法DANYELZA(naxitamab-gqgk),这是第一种被FDA批准用于骨髓或骨髓异位高危神经母细胞瘤患者,用于部分缓解、轻微缓解或稳定疾病之后的病情复发或难治性患者的治疗方案。

Mr. Pfreundschuh will be based in Y-mAbs' New York and New Jersey offices.

本新闻稿中有关未来期望、计划和前景的声明,以及任何其他关于不是历史事实的事项的声明,均可能构成《证券法》第27A条和第21E条所述的“前瞻性声明”。诸如 “预计”、“相信”、“考虑”、“继续”、“可能”、“估计”、“期望”、“希望”、“打算”、“可能”、“计划”、“潜在”、“预测”、“项目”、“应”、“目标”、“将”、“愿景”等类似表达未来态势的用语,旨在确定前瞻性声明,但并非所有前瞻性声明都包含这些区分符号。我们的产品候选人和相关技术是癌症治疗的新方法,存在重大挑战。由于各种因素,这些前瞻性声明或者保留各种与其相关的不确定性和重大风险,实际结果可能与此相差甚远。您不应过分依赖前瞻性声明,这些前瞻性声明仅有效期截至本新闻稿发布之日,公司不承担义务更新任何前瞻性声明,无论是基于新信息、未来事件还是其他因素。

About Y-mAbs
Y-mAbs is a commercial-stage biopharmaceutical company focused on the development and commercialization of novel, radioimmunotherapy, and antibody-based therapeutic cancer products. The Company's technologies include its investigational Self-Assembly DisAssembly ("SADA") Pretargeted Radioimmunotherapy Platform ("PRIT") and bispecific antibodies generated using the Y-BiClone platform. The Company's product pipeline includes the anti-GD2 therapy DANYELZA(naxitamab-gqgk), the first FDA-approved treatment for patients with relapsed or refractory high-risk neuroblastoma in the bone or bone marrow after a partial response, minor response, or stable disease to prior therapy.

关于Y-mAbs
DANYELZA和Y-mAbs是Y-mAbs Therapeutics, Inc.的注册商标。DANYELZA(naxitamab-gqgk)是FDA已批准的治疗复发性或难治高危神经母细胞瘤患者的第一种药物,在部分缓解、轻微缓解或稳定疾病之后,可以用于骨髓或骨髓异位部位治疗。

Forward-Looking Statements
Statements in this press release about future expectations, plans and prospects, as well as any other statements regarding matters that are not historical facts, may constitute "forward-looking statements" within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934. Such statements include, but are not limited to, statements about the Company's expectation that, with its new Chief Financial Officer, it is in a position to make strategic decisions that will serve its mission of improving the lives of patients with cancer and other serious diseases; the future of the Company's business, including with respect to expansion and its goals; the promising future of the Company; expectations with respect to the Company's products and product candidates, including potential territory expansion of DANYELZA and the potential market opportunity related thereto and the advancement and potential benefits thereof, and the potential of the SADA Technology and potential benefits and applications thereof; statements with respect to DANYELZA as a growing commercial product and SADA as a differentiated radioimmunotherapy platform; and other statements that are not historical facts. Words such as ''anticipate,'' ''believe,'' "contemplate," ''continue,'' ''could,'' ''estimate,'' ''expect,'' "hope," ''intend,'' ''may,'' ''might,'' ''plan,'' ''potential,'' ''predict,'' ''project,'' ''should,'' ''target,'' "will", ''would'', "guidance," and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. Our product candidates and related technologies are novel approaches to cancer treatment that present significant challenges. Actual results may differ materially from those indicated by such forward-looking statements as a result of various factors, including but not limited to: risks associated with the Company's financial condition and need for additional capital; the risks that actual results of the Company's restructuring plan and revised business plan will not be as expected; risks associated with the Company's development work; cost and success of the Company's product development activities and clinical trials; the risks of delay in the timing of the Company's regulatory submissions or failure to receive approval of its drug candidates; the risks related to commercializing any approved pharmaceutical product including the rate and degree of market acceptance of product candidates; development of sales and marketing capabilities and risks associated with failure to obtain sufficient reimbursement for products; the risks related to the Company's dependence on third parties including for conduct of clinical testing and product manufacture; the Company's inability to enter into partnerships; the risks related to government regulation; risks related to market approval, risks associated with protection of the Company's intellectual property rights; risks related to employee matters and managing growth; risks related to the Company's common stock, risks associated with macroeconomic conditions, including the conflict between Russia and Ukraine and sanctions related thereto, the state of war between Israel and Hamas and the related risk of a larger regional conflict, inflation, increased interest rates, uncertain global credit and capital markets and disruptions in banking systems; and other risks and uncertainties affecting the Company including those described in the "Risk Factors" section included in the Company's Annual Report on Form 10-K for the fiscal year ended December 31, 2023, the Company's Quarterly Report on Form 10-Q for the quarter ended March 31, 2024 and future filings and reports by the Company. Any forward-looking statements contained in this press release speak only as of the date hereof, and the Company undertakes no obligation to update any forward-looking statement, whether as a result of new information, future events or otherwise.

前瞻性声明
本新闻稿中有关未来期望、计划和前景的声明,以及任何其他关于不是历史事实的事项的声明,均可能构成《证券法》第27A条和第21E条所述的“前瞻性声明”。这些声明包括,但不限于,公司新任首席财务官将使财务结构更强大,从而更好地服务于改善癌症等重大疾病患者生活的使命;公司未来事业的发展,包括扩张和目标等;公司的产品和产品候选药物前景光明,包括DANYELZA的可能扩展区域以及市场机会和SADA技术的可能优势和应用等;DANYELZA作为增长中的商业产品和SADA作为不同的放射免疫治疗平台等。关键是,这些前瞻性声明可能与实际结果根据各种因素而有所不同,包括但不限于:公司的财务状况和需要额外的资本的风险;公司重组计划和修订业务计划的实际结果不如预期的风险;相关的开发工作的风险;公司产品开发活动和临床试验成本和成功率的风险;提交监管申请的时间延误的风险或未能获得药物候选人的批准;与商业化任何获得批准的药品有关的风险,包括产品候选人的市场接受率和市场开发的费用;开发销售和营销能力的风险;公司依赖于第三方包括进行临床检测和产品制造的风险;公司无法与他人建立合作关系的风险;与政府监管相关的风险;与市场批准有关的风险;与保护公司知识产权权利相关的风险;与员工问题和管理增长有关的风险;与公司普通股风险有关的风险;涉及宏观经济状况的风险,包括俄罗斯和乌克兰之间的冲突、制裁相关的风险、以色列和哈迈斯之间的战争状态以及有关更大的地区冲突的风险、通货膨胀、利率上涨、全球信贷和资本市场不确定以及银行系统瘫痪等因素的风险,以及公司未来的风险和不确定性,包括在2023财年结束的公司年报上的“风险因素”部分、2024年3月31日的公司季度报告以及公司未来的提交和报告。本新闻稿中的任何前瞻性声明仅适用于本新闻稿发布之日,并且公司没有义务更新任何前瞻性声明,也无义务因为新信息、未来事件或其他因素更新任何前瞻性声明。

DANYELZA and Y-mAbs are registered trademarks of Y-mAbs Therapeutics, Inc.

DANYELZA和Y-mAbs是Y-mAbs Therapeutics, Inc.的注册商标。

Investor Contact:
Courtney Dugan
VP, Head of Investor Relations
[email protected]

投资者联系人:
Courtney Dugan
VP,投资者关系负责人
[email protected]

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Source: Y-mAbs Therapeutics, Inc.

出处:Y-mAbs Therapeutics,Inc.

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