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New Interim Venous Ulcer Healing Data From the EnVVeno Medical VenoValve(R) Pivotal Trial to Be Presented at the Society for Vascular Surgery 2024 Vascular Annual Meeting on June 21, 2024

New Interim Venous Ulcer Healing Data From the EnVVeno Medical VenoValve(R) Pivotal Trial to Be Presented at the Society for Vascular Surgery 2024 Vascular Annual Meeting on June 21, 2024

2024年6月21日,EnVVeno 醫療公司 VenoValve(R) 關鍵試驗的新中期靜脈潰瘍癒合數據將在 2024 年血管年會上展示。
Accesswire ·  06/18 00:00

IRVINE, CA / ACCESSWIRE / June 17, 2024 / enVVeno Medical Corporation (Nasdaq:NVNO) ("enVVeno" or the "Company"), a company setting new standards of care for the treatment of venous disease, today announced that new interim venous ulcer healing data from the VenoValve U.S. pivotal trial will be presented at the Society for Vascular Surgery 2024 Vascular Annual Meeting (VAM2024) being held June 18-22, 2024 in Chicago, IL. The presentation, entitled "The Impact of VenoValve Implantation on Venous Ulcer Healing in Patients with Deep Venous Reflux," will be made on Friday, June 21, 2024 by primary investigator Dr. Cassius Iyad Ochoa Chaar MD, MS, RPVI, Associate Professor of Surgery, Division of Vascular Surgery, Yale School of Medicine, the top enrolling site for the trial.

enVVeno醫療公司(Nasdaq:NVNO)(“enVVeno”或“公司”)是一家爲靜脈疾病治療制定新標準的公司。它今天宣佈,來自VenoValve美國關鍵試驗的新的中期靜脈潰瘍癒合數據將在2024年6月18日至22日在伊利諾伊州芝加哥舉行的2024年血管年會(VAM2024)上公佈。此次發佈的題目是“VenoValve植入對患有下肢靜脈逆流的靜脈潰瘍癒合的影響”,由主要調查員Cassius Iyad Ochoa Chaar醫學博士、外科學副教授、血管外科學部的耶魯醫學院,該醫學院是該次試驗的最佳招募站,在6月21日星期五發布。VenoValve植入對患有下肢靜脈逆流的靜脈潰瘍癒合的影響今年的研究最重要的招募站雅芳·醫學院血管外科的心臟外科醫生塞倫·衆(VenVPoCir)。他有一個團隊,被重點研究的病例都是拉斐爾是什麼,VLCRP及阿洛伊斯·戈司以及其他心血管方面的問題。

The data to be presented will include venous ulcer healing and improvement rates for venous ulcer patients who have now reached the one-year milestone in the Company's Surgical Anti-reflux Venous Valve Endoprosthesis (SAVVE) U.S. pivotal study for the VenoValve. Overall healing or improvement rate data for thirty-one ulcers among twenty-one patients will be presented, and the presentation will also include sub-categories for ulcers that existed for more than one year and less than one year prior to the VenoValve surgery. Recurrence rate data for any venous ulcers that fully healed, and then recurred, will also be presented. Excerpts from the presentation will be made available on the Company's website.

在該公司的手術體系設計改進(SAVVE)美國關鍵研究中,治療靜脈潰瘍的數據將包括現已達到一年裏程碑的靜脈潰瘍癒合和改善率。共呈現了21位患者的31個潰瘍的整體癒合或改善率數據,這次發佈還將包括在VenoValve手術之前存在一年以上和一年以下的潰瘍的亞類別。對於任何完全癒合,然後復發的靜脈潰瘍的複發率數據也將被提供。從報告中摘錄的內容也將在公司網站上公開。S手術A抗反流V靜脈V門瓣E內植物(SAVVE)

In assessing the benefit and risk of a novel technology such as the VenoValve, which addresses an unmet medical need, the U.S. Food and Drug Administration (FDA) considers whether a medical device provides a clinically meaningful benefit compared to existing technologies. Subjects with venous ulcers who were enrolled in the SAVVE study all received at least three (3) months of conventional treatment with existing technologies (compression therapy, leg elevation, and wound care) and many also received vein ablations for superficial venous disease, and venous stenting for obstruction, if indicated. As a result, the venous ulcer patients in the SAVVE study are the most difficult to treat, having venous ulcers that remained after at least three and as many as five types of existing treatments.

在評估VenoValve這種解決未滿足的醫療需求的新技術的收益和風險時,美國食品和藥物管理局(FDA)考慮醫療設備是否提供與現有技術相比的臨床有意義的益處。參加SAVVE研究的患有靜脈潰瘍的受試者均接受了至少三個月的常規治療(壓縮治療、抬高腿部位置和創面護理),許多人還接受了針對表淺靜脈疾病的靜脈消融和靜脈梗阻的靜脈支架植入等治療。因此,SAVVE研究中的靜脈潰瘍患者是最難治療的,大部分病人已經接受了至少三種,最多五種的現有治療技術。

Severe Chronic Venous Insufficiency (CVI) is a debilitating disease that most often occurs when valves inside of the veins of the leg fail, causing blood to flow in the wrong direction (reflux) and increased pressure within the veins of the leg (venous hypertension). Symptoms of severe CVI include leg swelling, pain, edema, and recurrent open sores known as venous ulcers. The disease can severely impact everyday functions such as sleeping, bathing, and walking, and is known to result in high rates of depression and anxiety. There are currently no effective treatments for severe CVI of the deep vein system caused by valvular incompetence and the Company estimates that there are approximately 2.5 million new patients each year in the U.S. that could be candidates for the VenoValve.

嚴重的慢性靜脈功能不全(CVI)是一種嚴重的疾病,當腿部靜脈內的瓣膜功能失敗時,會導致血液逆向流動(反流)以及腿部靜脈壓力增加(靜脈高壓)。嚴重CVI的症狀包括腿部腫脹、疼痛、水腫和反覆出現的潰瘍,稱爲靜脈性潰瘍。這種疾病可以嚴重影響日常生活功能,如睡眠、沐浴和行走,並已知會導致高發的抑鬱症和焦慮症。目前沒有有效的治療方案,用於治療瓣膜功能障礙引起的深靜脈系統嚴重CVI,該公司估計每年在美國有大約250萬新患者可能成爲VenoValve的候選人。

The FDA has asked the Company to collect one year data on all SAVVE patients to support its PMA application seeking FDA approval to market and sell the VenoValve, which the Company expects to file in Q4 of this year. For more information about the 2024 Vascular Annual Meeting, please visit vascular.org/vam-2024.

FDA要求該公司收集所有SAVVE研究患者的一年數據,以支持其PMA申請,以獲得FDA批准營銷和銷售VenoValve,該公司預計將在本年第四季度提出申請。有關2024年血管年會的更多信息,請訪問vascular.org/vam-2024。

About enVVeno Medical Corporation

關於enVVeno Medical Corporation

enVVeno Medical (NASDAQ:NVNO) is an Irvine, California-based, late clinical-stage medical device Company focused on the advancement of innovative bioprosthetic (tissue-based) solutions to improve the standard of care for the treatment of venous disease. The Company's lead product, the VenoValve, is a potential first-in-class surgical replacement venous valve being developed for the treatment of deep venous Chronic Venous Insufficiency (CVI). The Company is also developing a non-surgical, transcatheter based replacement venous valve for the treatment of deep venous CVI called enVVe. CVI occurs when valves inside of the veins of the leg become damaged, resulting in the backwards flow of blood (reflux), blood pooling in the lower leg, increased pressure in the veins of the leg (venous hypertension) and in severe cases, venous ulcers that are difficult to heal and become chronic. Both the VenoValve and enVVe are designed to act as one-way valves, to help assist in propelling blood up the leg, and back to the heart and lungs. The VenoValve is currently being evaluated in the SAVVE U.S. pivotal trial and the Company is currently performing the final testing necessary to seek approval for the enVVe pivotal trial.

enVVeno Medical(納斯達克股票代碼:NVNO)是一家總部位於加利福尼亞州爾灣的晚期臨床階段醫療器械公司,專注於推進創新的生物義肢(基於組織的)解決方案,以改善治療靜脈疾病的標準。該公司的主要產品VenoValve是一種潛在的首創外科替代靜脈瓣膜,用於治療深靜脈慢性靜脈功能不全(CVI)。該公司還開發基於非手術的介入替換靜脈瓣:enVVe,用於治療深靜脈CVI。當腿部的靜脈內瓣膜損壞時,CVI會發生,導致血液回流(反流)、血液滯留於下肢,靜脈高壓以及在嚴重情況下難以癒合並變爲慢性的靜脈潰瘍。VenoValve和enVVe都設計爲單向閥門,以幫助推動血液上行到腿部,並返回心臟和肺部。目前,VenoValve正處於SAVVE美國關鍵試驗中的評估階段,該公司正在進行最終測試,以尋求enVVe關鍵試驗的批准。

Cautionary Note on Forward-Looking Statements

前瞻性聲明的警示說明

This press release and any statements of stockholders, directors, employees, representatives and partners of enVVeno Medical Corporation (the "Company") related thereto contain, or may contain, among other things, certain "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995. Such forward-looking statements involve significant risks and uncertainties. Such statements may include, without limitation, statements identified by words such as "projects," "may," "will," "could," "would," "should," "believes," "expects," "anticipates," "estimates," "intends," "plans," "potential" or similar expressions. These statements are based upon the current beliefs and expectations of the Company's management and are subject to significant risks and uncertainties, including those detailed in the Company's filings with the Securities and Exchange Commission. Actual results and timing may differ significantly from those set forth or implied in the forward-looking statements. Forward-looking statements involve certain risks and uncertainties that are subject to change based on various factors (many of which are beyond the Company's control). The Company undertakes no obligation to publicly update any forward-looking statements, whether as a result of new information, future presentations or otherwise, except as required by applicable law.

本新聞稿以及與enVVeno Medical Corporation(以下簡稱“公司”)的股東、董事、員工、代表和合作夥伴有關的任何聲明可能包含或可能包含其他內容,除此之外,還包含某些《1995年私人證券訴訟改革法》規定的重要風險和不確定性。這種前瞻性聲明可能包括無關語句,例如“計劃”、“可能”、“將”,“可能”,“應該”,“相信”、“期望”、“預期”、“估計”、“意圖”、“計劃”、“潛力”或類似表達。這些聲明基於公司管理層的當前信仰和期望,並且受到重大的風險和不確定性的影響,包括那些在公司向證券交易委員會提交的文件中詳細描述的風險和不確定性。實際結果和時間可能會與前瞻性聲明所設定或暗示的結果和時間顯著不同。前瞻性聲明涉及某些風險和不確定性,這些風險和不確定性可能基於各種因素髮生變化(其中許多因素超出了公司的控制範圍)。公司無需公開更新任何前瞻性聲明,無論是因爲新的信息,還是由於未來的報告或其他原因,除非法律規定。

INVESTOR CONTACT:

投資者聯繫方式:

Jenene Thomas, JTC Team, LLC
NVNO@jtcir.com
(833) 475-8247

Jenene Thomas,JTC團隊LLC
NVNO@jtcir.com
(833) 475-8247

SOURCE: enVVeno Medical

來源:enVVeno Medical


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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