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Shockwave Medical Enrolls First Patient in Disrupt BTK II Study for Long, Calcified, Below the Knee Lesions

Shockwave Medical Enrolls First Patient in Disrupt BTK II Study for Long, Calcified, Below the Knee Lesions

Shockwave Medical公司招募第一名患者參加Disrupt BTK II研究,研究對象為膝關節以下的長期鈣化病變
GlobeNewswire ·  2021/11/22 21:10

Global Post-Market Study Will Assess Long-Term Benefit of Peripheral IVL on the Most Challenging Calcified Lesions, Including Patients with Critical Limb Ischemia

全球上市後研究將評估外周IVL對包括嚴重肢體缺血患者在內的最具挑戰性的鈣化病變的長期益處

SANTA CLARA, Calif., Nov. 22, 2021 (GLOBE NEWSWIRE) -- Shockwave Medical, Inc. (NASDAQ: SWAV), a pioneer in the development of Intravascular Lithotripsy (IVL) to treat severely calcified cardiovascular disease, today announced the start of the Disrupt BTK II post-market study to assess the safety, effectiveness and optimal clinical use of the Shockwave Peripheral IVL System for the treatment of calcified peripheral lesions below the knee (BTK), including some of the most challenging patients with critical limb ischemia (CLI).

加利福尼亞州聖克拉拉,2021年11月22日(環球通訊社)--衝擊波醫療公司(納斯達克代碼:SWAV)是開發血管內碎石術治療嚴重鈣化心血管疾病的先驅,該公司今天宣佈啟動Disrupt BTK II上市後研究,以評估Shockwave外周體外碎石術系統治療膝關節以下鈣化周圍病變的安全性、有效性和最佳臨牀應用,包括

Disrupt BTK II is a post-market, prospective, multicenter, single-arm study led by Ehrin Armstrong, M.D., Medical Director and Interventional Cardiologist, Adventist Heart & Vascular Institute, and Venita Chandra, M.D., Vascular Surgeon and Clinical Associate Professor, Division of Vascular Surgery, Stanford Health Care. The study is expected to enroll 250 patients across 40 sites globally that will be followed for two years to assess the long-term durability of IVL in this difficult to treat patient population. The first Disrupt BTK II patient was enrolled at Midwest Cardiovascular Research Foundation by Dr. Nicolas Shammas.

Disrupt BTK II是一項上市後、前瞻性、多中心、單臂研究,由基督復臨安息日會心臟與血管研究所醫學主任兼介入心臟病學家Ehrin Armstrong醫學博士和斯坦福醫療保健公司血管外科醫學博士、血管外科臨牀副教授Venita Chandra領導。這項研究預計將在全球40個地點招募250名患者,並將進行為期兩年的跟蹤調查,以評估IVL在這一難以治療的患者羣體中的長期持久性。美國中西部心血管研究基金會的尼古拉斯·沙馬斯博士招募了首位Disrupt BTK II患者。

"Patients with severely calcified, diffuse below the knee disease, and especially those with critical limb ischemia, are often in severe pain with limited treatment options to achieve adequate arterial revascularization. The unmet clinical need for this population is extremely high," said Dr. Armstrong. "Disrupt BTK II will further evaluate how IVL may be optimally used to treat patients who have historically been excluded from most endovascular treatment trials."

阿姆斯特朗博士説:“患有嚴重鈣化、瀰漫在膝關節以下的患者,尤其是肢體嚴重缺血的患者,往往疼痛劇烈,實現充分的動脈血運重建的治療選擇有限。這一人羣尚未得到滿足的臨牀需求非常高。”Disrupt BTK II將進一步評估如何以最佳方式使用IVL治療歷史上被排除在大多數血管內治療試驗之外的患者。“

The primary effectiveness endpoint of Disrupt BTK II is procedural success, defined as ≤50 percent residual stenosis for all treated target lesions without serious angiographic complications (flow-limiting dissection, perforation, distal embolization, or acute vessel closure), as assessed by an independent angiographic core lab. The study will assess the absence of major adverse limb events (MALE) within 30 days of the index procedure as a primary safety endpoint.

Disrupte BTK II的主要療效終點是操作成功,由獨立的血管造影核心實驗室評估,定義為所有治療的目標病變的≤50%殘餘狹窄,沒有嚴重的血管造影併發症(限流性夾層、穿孔、遠端栓塞或急性血管關閉)。這項研究將評估指標操作後30天內是否出現主要不良肢體事件(男性),作為主要安全終點。

"More and more patients with CLI also present with end-stage renal disease, advanced diabetes, or other comorbidities that impact their overall health and our ability to effectively treat their CLI," said Dr. Chandra. "We already know that IVL can reduce significant dissection as well as reduce the need for provisional stenting over conventional PTA in peripheral vessel beds, but what makes Disrupt BTK II even more exciting is that we are now isolating the treatment effect to get a clearer picture about what role IVL can offer as a definitive therapy for these very complex patients."

錢德拉博士説:“越來越多的CLI患者還出現終末期腎病、晚期糖尿病或其他影響他們整體健康和我們有效治療CLI的能力的併發症。”我們已經知道,與傳統的PTA相比,IVL可以減少嚴重的夾層,並減少在外周血管牀上臨時植入支架的需要,但更令人興奮的是,我們現在正在隔離治療效果,以便更清楚地瞭解IVL作為這些非常複雜的患者的最終療法可以起到什麼作用。“

About Shockwave Medical, Inc.
Shockwave is focused on developing and commercializing products intended to transform the way calcified cardiovascular disease is treated. Shockwave aims to establish a new standard of care for the interventional treatment of atherosclerotic cardiovascular disease through differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque, which the company refers to as Intravascular Lithotripsy (IVL). IVL is a minimally invasive, easy-to-use and safe way to significantly improve patient outcomes. To view an animation of the IVL procedure and for more information, visit www.shockwavemedical.com.

關於衝擊波醫療公司
Shockwave專注於開發和商業化旨在改變鈣化心血管疾病治療方式的產品。Shockwave旨在為動脈粥樣硬化性心血管疾病的介入治療建立一種新的護理標準,通過差異化和專有的局部聲波壓力波治療鈣化斑塊,該公司將其稱為血管內碎石術(IVL)。IVL是一種微創、易用和安全的方法,可以顯著改善患者的預後。要觀看IVL過程的動畫並瞭解更多信息,請訪問www.shockwave emedical.com。

Forward-Looking Statements
This press release contains statements relating to our expectations, projections, beliefs, and prospects, which are "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995. In some cases, you can identify these statements by forward-looking words such as "may," "might," "will," "should," "expects," "plans," "anticipates," "believes," "estimates," "predicts," "potential" or "continue," and similar expressions, and the negative of these terms. You are cautioned not to place undue reliance on these forward-looking statements. Forward-looking statements are only predictions based on our current expectations, estimates, and assumptions, valid only as of the date they are made, and subject to risks and uncertainties, some of which we are not currently aware.

前瞻性陳述
本新聞稿包含與我們的預期、預測、信念和前景有關的陳述,這些陳述屬於1995年“私人證券訴訟改革法案”所指的“前瞻性陳述”。在某些情況下,您可以通過“可能”、“可能”、“將會”、“應該”、“預期”、“計劃”、“預期”、“相信”、“估計”、“預測”、“潛在”或“繼續”等前瞻性詞語以及類似的表達方式,以及這些術語的負面含義來識別這些陳述。告誡您不要過度依賴這些前瞻性陳述。前瞻性陳述僅是基於我們目前的預期、估計和假設做出的預測,僅在它們作出之日有效,會受到風險和不確定性的影響,其中一些風險和不確定性我們目前還沒有意識到。

Important factors that could cause our actual results and financial condition to differ materially from those indicated in the forward-looking statements include, among others: the impact of the COVID-19 pandemic on our operations, financial results, and liquidity and capital resources, including the impact on our sales, expenses, supply chain, manufacturing, research and development activities, clinical trials, and employees; our ability to develop, manufacture, obtain and maintain regulatory approvals for, market and sell, our products; our expected future growth, including the size and growth potential of the markets for our products; our ability to obtain coverage and reimbursement for procedures performed using our products; our ability to scale our organizational culture; the impact of the development, regulatory approval, efficacy and commercialization of competing products; the loss of key scientific or management personnel; our ability to develop and maintain our corporate infrastructure, including our internal controls; our financial performance and capital requirements; and our ability to obtain and maintain intellectual property protection for our products, as well as our ability to operate our business without infringing the intellectual property rights of others. These factors, as well as others, are discussed in our filings with the Securities and Exchange Commission (SEC), including in Part I, Item IA - Risk Factors in our most recent Annual Report on Form 10-K filed with the SEC, and in our other periodic and other reports filed with the SEC. Except to the extent required by law, we do not undertake to update any of these forward-looking statements after the date hereof to conform these statements to actual results or revised expectations

可能導致我們的實際結果和財務狀況與前瞻性陳述中顯示的結果大不相同的重要因素包括但不限於:新冠肺炎疫情對我們的運營、財務業績、流動性和資本資源的影響,包括對我們的銷售、費用、供應鏈、製造、研發活動、臨牀試驗和員工的影響;我們開發、製造、獲得和維持監管部門對我們產品的批准、營銷和銷售的能力;我們預期的未來增長,包括我們產品市場的規模和增長潛力;我們獲得保險和報銷的能力。這些因素包括:我們擴大組織文化的能力;競爭產品的開發、監管批准、效力和商業化的影響;關鍵科學或管理人員的流失;我們開發和維護公司基礎設施(包括內部控制)的能力;我們的財務業績和資本要求;以及我們為產品獲得和維護知識產權保護的能力,以及我們在不侵犯他人知識產權的情況下運營業務的能力。這些因素以及其他因素已在我們提交給美國證券交易委員會(美國證券交易委員會)的文件中進行了討論,包括在我們提交給美國證券交易委員會的最新10-K表格年度報告中的第I部分IA項-風險因素,以及我們提交給美國證券交易委員會的其他定期報告和其他報告中。除法律要求的範圍外,我們不承諾在本新聞稿發佈之日後更新這些前瞻性陳述中的任何一項,以使這些陳述與實際結果或修訂後的預期相符。

Media Contact:
Scott Shadiow
+1.317.432.9210
sshadiow@shockwavemedical.com

媒體聯繫人:
斯科特·沙迪奧
+1.317.432.9210
郵箱:sshadiow@shockwave emedical.com

Investor Contact:
Debbie Kaster
dkaster@shockwavemedical.com

投資者聯繫方式:
黛比·卡斯特
郵箱:dkaster@shockwave emedical.com


譯文內容由第三人軟體翻譯。


以上內容僅用作資訊或教育之目的,不構成與富途相關的任何投資建議。富途竭力但無法保證上述全部內容的真實性、準確性和原創性。
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