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Boston Scientific Obtains CE Mark for ACURATE Prime Aortic Valve System

Boston Scientific Obtains CE Mark for ACURATE Prime Aortic Valve System

波士顿科学获得ACURATE Prime主动脉瓣系统的CE标志。
PR Newswire ·  08/27 06:57

MARLBOROUGH, Mass., Aug. 27, 2024 /PRNewswire/ -- Boston Scientific Corporation (NYSE: BSX) today announced it has obtained CE mark for the ACURATE Prime Aortic Valve System, the newest transcatheter aortic valve replacement (TAVR) technology in the company's structural heart portfolio. The ACURATE Prime valve system is designed with several features to build upon the clinical performance of the ACURATE neo2 platform including an additional valve size, which expands the treatment range to patients with a larger anatomy.

波士顿科学公司(纽交所:BSX)今日宣布,其最新转导主动脉瓣系统ACURATE Prime获得CE标志,这是该公司结构性心脏产品组合中最新的经导管主动脉瓣置换(TAVR)技术。ACURATE Prime主动脉瓣系统采用了多项功能,以便在ACURATE neo2平台的临床性能的基础上进一步提高,包括一个额外的瓣膜尺寸,将治疗范围扩大到有较大解剖结构的患者。

Video: ACURATE Prime Aortic Valve System
视频:ACURATE Prime经导管主动脉瓣系统
ACURATE Prime Aortic Valve System
ACURATE Prime经导管主动脉瓣系统

The new ACURATE Prime valve system is indicated to restore function and normal blood flow through a narrowed aortic valve in low, intermediate and high-risk patients with severe aortic stenosis. With a self-expanding, supra-annular design, this device has an enhanced frame that equalizes force across the valve for a stable fit against the native, diseased valve. It also offers physicians a redesigned deployment mechanism for highly accurate valve positioning to help ensure positive patient outcomes.

ACURATE Prime瓣系统适用于低、中和高风险重症主动脉狭窄患者,以恢复狭窄的主动脉瓣的功能和正常血液流动。该装置采用了自扩张的象限上方设计,具有增强的框架,可使阀门稳固贴合在原有的病变阀门上,并均衡施加力量。它还提供医生重新设计的部署机制,以实现高精确的阀位,确保患者的阳性结果。

"The introduction of the ACURATE Prime technology offers physicians a TAVR option designed for streamlined procedural preparation, improved performance in complex cases and simplified delivery for quick and controlled deployment," said Janar Sathananthan, M.D., chief medical officer, Interventional Cardiology Therapies, Boston Scientific. "Further, our clinical experience with the valve to date has shown the ability for precise positioning of the device in a broader population of patients, allowing more clinicians to consider this technology for treatment in challenging or larger heart structures."

波士顿科学介入心脏病学治疗的首席医学官Janar Sathananthan万.D.表示:“ACURATE Prime技术的推出为医生提供了一种经导管主动脉瓣置换选项,旨在简化手术准备流程,提高复杂病例的性能,并简化交付,以快速而精确的部署。”我们对该瓣膜迄今的临床经验显示,能够在更广泛的患者群体中精确定位设备,使更多临床医生考虑在具有挑战性或更大的心脏结构的患者中使用这项技术。

The ACURATE Prime valve system will now be available for the treatment of aortic annulus diameters between 20.5 and 29 mm. It will also carry through many of the design features and clinical outcomes demonstrated in global studies with the ACURATE neo2 platform, including low pacemaker and paravalvular leak rates,1,2 strong hemodynamic performance,1 as well as unrestricted coronary access for future procedures.

ACURATE Prime瓣系统现在可以用于治疗20.5至2900万之间的主动脉环直径。它还延续了全球研究中ACURATE neo2平台所展示的许多设计特点和临床结果,包括低起搏器和瓣周漏率、强大的血流动力学性能,以及未来操作的不受限制的冠状动脉通道。

"We are thrilled to offer physicians a new valve with meaningful improvements for the treatment of an increasing number of patients with aortic valve disease," said Lance Bates, senior vice president and president, Interventional Cardiology Therapies, Boston Scientific. "Built on the ACURATE valve platform, which has been implanted in nearly 80,000 patients globally to date, the ACURATE Prime valve system is engineered to improve long-term cardiac function and provide access for future treatment needs, thereby supporting the lifetime management of these patients."

“我们很高兴能为越来越多患有主动脉瓣病的患者提供具有实质性改进的新型瓣膜。”波士顿科学公司介入心脏治疗业务高级副总裁兼总裁兰斯·贝茨表示:“ACURATE瓣膜平台已在全球范围内植入近8万名患者身上,ACURATE Prime瓣膜系统的工程设计可以改善长期心脏功能,为未来的治疗需求提供入路,从而支持这些患者的终身管理。”

The company will initiate the launch of the ACURATE Prime valve system in Europe in the coming weeks. For more information on the system, visit .

该公司将在未来几周内在欧洲推出ACURATE Prime瓣膜系统。有关该系统的更多信息,请访问 。

*In Europe, the ACURATE neo2 Aortic Valve System and the ACURATE Prime Aortic Valve System are CE-marked. In the USA, the ACURATE neo2 Aortic Valve System and the ACURATE Prime Aortic Valve System are investigational devices and are restricted under federal law to investigational use only. Not available for sale.

*在欧洲,ACURATE neo2主动脉瓣系统和ACURATE Prime主动脉瓣系统已经获得CE标志。在美国,ACURATE neo2主动脉瓣系统和ACURATE Prime主动脉瓣系统是研究性设备,仅限于进行研究性使用,不能出售。

About Boston Scientific
Boston Scientific transforms lives through innovative medical technologies that improve the health of patients around the world. As a global medical technology leader for more than 45 years, we advance science for life by providing a broad range of high-performance solutions that address unmet patient needs and reduce the cost of health care. Our portfolio of devices and therapies helps physicians diagnose and treat complex cardiovascular, respiratory, digestive, oncological, neurological and urological diseases and conditions. Learn more at and connect on LinkedIn and X, formerly Twitter.

关于波士顿科学
波士顿科学通过创新医疗技术改善世界各地患者的健康,改变他们的生活。作为全球医疗技术领先企业,我们致力于为患者提供一系列高性能解决方案,满足未满足的患者需求,并降低医疗保健成本。我们的设备和疗法产品组合帮助医生诊断和治疗复杂的心血管、呼吸、消化、肿瘤、神经和泌尿系统疾病和病症。了解更多,请访问网址 ,并在LinkedIn和X(以前的Twitter)上进行交流。

Cautionary Statement Regarding Forward-Looking Statements

关于前瞻性声明的警示声明

This press release contains 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. Forward-looking statements may be identified by words like "anticipate," "expect," "project," "believe," "plan," "estimate," "intend" and similar words. These forward-looking statements are based on our beliefs, assumptions and estimates using information available to us at the time and are not intended to be guarantees of future events or performance. These forward-looking statements include, among other things, statements regarding our business plans and product performance and impact, and new and anticipated product approvals and launches. If our underlying assumptions turn out to be incorrect, or if certain risks or uncertainties materialize, actual results could vary materially from the expectations and projections expressed or implied by our forward-looking statements. These factors, in some cases, have affected and in the future (together with other factors) could affect our ability to implement our business strategy and may cause actual results to differ materially from those contemplated by the statements expressed in this press release. As a result, readers are cautioned not to place undue reliance on any of our forward-looking statements.

本新闻稿包含根据1933年证券法第27A条和1934年证券交易法第21E条的前瞻性陈述。前瞻性陈述可能被识别出来,例如“预计”、“期望”、“计划”、“相信”、“估计”、“打算”等类似的字眼。这些前瞻性陈述基于我们在时候可得到的信仰、假设和估计,并且不打算作为未来事件或业绩的保证。这些前瞻性陈述包括但不限于关于我们的业务计划、产品业绩和影响、新产品的批准和发布等的声明。如果我们的基本假设被证明是不正确的,或者如果某些风险或不确定性出现,实际结果可能会与我们的前瞻性陈述表达的期望和预测有很大的差异。在某些情况下,这些因素已经影响了并且将来(与其他因素一起)可能会影响我们实施业务策略的能力,并导致实际结果与本新闻稿所表达的声明所预期的结果出现差异。因此,读者被警告不要过分依赖我们的任何前瞻性陈述。

Factors that may cause such differences include, among other things: future economic, competitive, reimbursement and regulatory conditions; manufacturing, distribution and supply chain disruptions and cost increases; variations in outcomes of ongoing and future clinical trials and market studies; new product introductions; demographic trends; intellectual property; litigation; financial market conditions; and future business decisions made by us and our competitors. All of these factors are difficult or impossible to predict accurately and many of them are beyond our control. For a further list and description of these and other important risks and uncertainties that may affect our future operations, see Part I, Item 1A – Risk Factors in our most recent Annual Report on Form 10-K filed with the Securities and Exchange Commission, which we may update in Part II, Item 1A – Risk Factors in Quarterly Reports on Form 10-Q we have filed or will file hereafter. We disclaim any intention or obligation to publicly update or revise any forward-looking statements to reflect any change in our expectations or in events, conditions or circumstances on which those expectations may be based, or that may affect the likelihood that actual results will differ from those contained in the forward-looking statements, except as required by law. This cautionary statement is applicable to all forward-looking statements contained in this document.

可能导致这些差异的因素包括但不限于:未来经济、竞争、报销和监管条件;制造、分销和供应链中断和成本增加;正在进行和将来进行的临床试验和市场研究结果的变化;新产品推出;人口统计趋势;知识产权;诉讼;金融市场条件;以及我们和竞争对手未来的业务决策。所有这些因素都难以准确预测,而且其中许多因素超出我们的控制范围。有关可能影响我们未来运营的其他重要风险和不确定性的进一步清单和描述,请参阅我们最近提交给证券交易委员会的年度报告Form 10-k的第I部分,第1A条 - 风险因素,我们可能在此之后更新的季度报告Form 10-Q的第II部分,第1A条 - 风险因素。我们不承担公开更新或修订任何前瞻性声明以反映我们对期望的任何变化或在可能影响实际结果可能与前瞻性声明中所含结果不同的事件、条件或情况上的期望,除非法律要求。此警告声明适用于本文件中包含的所有前瞻性声明。

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1 Rück A, Kim WK, Abdel-Wahab M, et al. The Early neo2 Registry: Transcatheter Aortic Valve Implantation with ACURATE neo2 in a European Population. J Am Heart Assoc. 2023 Aug;12(15):e029464.
2 Kim WK, Tamburino C, Möllmann H, et al. Clinical outcomes of the ACURATE neo2 transcatheter heart valve: a prospective, multicenter, observational, post-market surveillance study. EuroIntervention. 2023 May 12;19(1):83-92.

1. Ruück A, Kim Wk, Abdel-Wahab m等人。《早期neo2注册表:使用ACURATE neo2进行经导管主动脉瓣植入术在欧洲人群中的结果》。《美国心脏协会志》2023年8月;12(15):e029464。
2.Kim Wk, Tamburino C, Möllmann H等人。《ACURATE neo2经导管心脏瓣成像学临床结果:一项前瞻性、多中心、观察性、市场后期监测研究》。《EuroIntervention》2023年5月12日;19(1):83-92。

SOURCE Boston Scientific Corporation

资讯来源:波士顿科学

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