EnVVeno Medical Successfully Completes Final Wave of Implants in Pre-Clinical GLP Study for EnVVe
EnVVeno Medical Successfully Completes Final Wave of Implants in Pre-Clinical GLP Study for EnVVe
Successful Completion of All Planned Implants in GLP Study
成功完成GLP研究中所有計劃的植入
enVVe Delivery System Demonstrates Consistent Performance
enVVe輸送系統展示了一致的性能
Company Maintains Timeline for IDE Application Submission by Mid-2025, Pending GLP Study Results
公司保持在2025年中期提交IDE申請的時間表,等待GLP研究結果
IRVINE, CA / ACCESSWIRE / December 16, 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 the successful completion of the final wave of implants for shorter-term subjects in its six-month pre-clinical GLP study for enVVe, its transcatheter-delivered replacement venous valve.
加利福尼亞州歐文 / ACCESSWIRE / 2024年12月16日 / enVVeno醫療公司(納斯達克:NVNO)("enVVeno"或"公司"),一家爲靜脈疾病治療設定新護理標準的公司,今天宣佈爲其六個月的臨床前GLP研究成功完成了短期受試者的最後一波植入。
The successful completion of all planned implants in the GLP study, including both long-term and short-term subjects, completes a critical phase of the study. The follow-up period, which began with the first wave of implants, is ongoing as scheduled. Pending successful completion of the GLP study, the Company anticipates submitting its IDE application to the FDA in mid-2025. The submission, if approved, would allow the Company to initiate the pivotal clinical trial for enVVe.
成功完成GLP研究中所有計劃的植入,包括長期和短期受試者,完成了研究的關鍵階段。隨訪期從第一波植入開始,按計劃持續進行。待GLP研究成功完成,公司預計將在2025年中期向FDA提交其IDE申請。該申請若獲得批准,將允許公司啓動enVVe的關鍵臨床試驗。
"With the successful completion of all planned implants in the enVVe GLP study, we have achieved the last of our milestones for 2024," said Robert Berman, enVVeno Medical's Chief Executive Officer. "Our enhanced enVVe crimping and delivery system has performed very well throughout the study and is ready for the pivotal trial. We will continue to monitor the performance of the enVVe valves throughout the remainder of the study and with successful data and pathology, should be in a position to file the IDE on schedule in mid 2025. We remain focused on our goal of becoming the established leader in both the surgical and non-surgical replacement venous valve markets for patients with severe deep venous CVI."
「隨着enVVe GLP研究中所有計劃植入的成功完成,我們達成了2024年的最後一個里程碑,」enVVeno醫療公司首席執行官羅伯特·伯曼表示。「我們增強的enVVe壓縮和輸送系統在整個研究中表現非常出色,準備進行關鍵試驗。我們將繼續監測enVVe瓣膜在研究餘下部分的表現,若數據和病理結果成功,應能在2025年中期按時提交IDE申請。我們始終專注於成爲重度深靜脈CVI患者外科和非外科替代靜脈瓣市場的確立領導者。」
Severe, deep venous Chronic Venous Insufficiency (CVI) is a debilitating disease that is most often caused by blood clots (deep vein thromboses or DVTs) in the deep veins of the leg. When valves inside of the veins of the leg fail, blood flows in the wrong direction and pools in the lower leg, causing pressure within the veins of the leg to increase (venous hypertension). Symptoms of severe CVI include leg swelling, pain, edema, and in the most severe cases, recurrent open sores known as venous ulcers. The disease can severely impact everyday functions such as sleeping, bathing, dressing, 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. Estimates indicate that CVI costs the U.S. healthcare system in excess of $4 billion each year.
重度深靜脈慢性靜脈功能不全(CVI)是一種致殘性疾病,通常由腿部深靜脈中的血栓(深靜脈血栓形成或DVT)引起。當腿部靜脈內的瓣膜失效時,血液朝錯誤的方向流動並在小腿內淤積,導致腿部靜脈內的壓力增加(靜脈高血壓)。重度CVI的症狀包括腿部腫脹、疼痛、水腫,在最嚴重的情況下,出現稱爲靜脈性潰瘍的複發性開放性傷口。這種疾病可以嚴重影響日常功能,例如睡眠、洗澡、穿衣和行走,並且已知會導致高發的抑鬱和焦慮。目前沒有有效的治療方法可以解決由瓣膜功能不全引起的深靜脈系統的重度CVI。估計CVI每年給美國醫療系統造成超過40億美元的費用。
The Company's lead product is the VenoValve, a potential first-in-class, surgical replacement venous valve for patients with severe deep venous CVI. In November, the Company submitted a PMA application with the U.S. Food and Drug Administration seeking approval to market and sell the VenoValve in the U.S. The Company estimates that there are approximately 2.5 million potential new patients each year in the U.S. that could be candidates for the VenoValve. The Company is also developing enVVe, a next-generation, transcatheter based replacement venous valve, that could appeal to an even larger market in terms of both patients and physicians.
公司的主打產品是VenoValve,這是一種潛在的首創外科手術更換靜脈瓣,適用於嚴重深靜脈慢性靜脈功能不全(CVI)患者。在11月, 公司向美國食品和藥物管理局提交了一份PMA申請,尋求在美國市場和銷售VenoValve的批准。公司估計,美國每年大約有250萬名潛在新患者可能成爲VenoValve的候選者。公司還在開發enVVe,這是一種基於導管的下一代更換靜脈瓣,可能吸引更大市場的患者和醫生。
Beginning early next year, the Company will begin to implement its strategy to transition from a development stage to a commercial entity for the VenoValve, while completing the necessary non-clinical and GLP testing for enVVe in preparation for its IDE application.
從明年初開始,公司將開始實施其策略,將VenoValve的開發階段轉變爲商業實體,同時完成enVVe的必要非臨床和GLP測試,以爲其IDE申請做好準備。
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 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 study and the Company is currently performing the final testing necessary to seek approval for the pivotal trial for enVVe.
enVVeno Medical(納斯達克:NVNO)是一家位於加利福尼亞爾灣的晚期臨床階段醫療器械公司,專注於推動創新生物假體(基於組織的)解決方案,以改善靜脈疾病治療的標準。從的主打產品VenoValve是一種首創的外科手術更換靜脈瓣,旨在治療深靜脈慢性靜脈功能不全(CVI)。公司還在開發一種用於治療深靜脈CVI的非外科、基於導管的更換靜脈瓣,稱爲enVVe。CVI發生在腿部靜脈內的瓣膜受到損害時,導致血液反向流動(返流)、血液在小腿處聚集、腿部靜脈壓力增加(靜脈高血壓),在嚴重情況下會出現難以癒合的靜脈潰瘍,並且變得慢性。VenoValve和enVVe都設計爲單向瓣膜,幫助推動血液上行到腿部,並返回心臟和肺部。VenoValve目前在SAVVE美國關鍵研究中進行評估,公司正在進行最終測試,以尋求對enVVe關鍵試驗的批准。
Cautionary Note on Forward-Looking Statements
關於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.
本新聞稿及enVVeno Medical Corporation(「公司」)的股東、董事、員工、代表和合夥人相關的任何聲明含有或可能含有在1995年《私人證券訴訟改革法》意義上的某些「前瞻性陳述」。這些前瞻性陳述涉及重大風險和不確定性。這些陳述可能包括但不限於使用「項目」、「可能」、「將」、「可以」、「會」、「應該」、「相信」、「期望」、「預期」、「估計」、「打算」、「計劃」、「潛在」或類似表達的陳述。這些陳述基於公司管理層當前的信念和期望,並受到重大風險和不確定性的制約,包括在公司向證券交易委員會的文件中詳細列出的風險。實際結果和時機可能與前瞻性陳述中所設定或暗示的內容存在顯著差異。前瞻性陳述涉及某些風險和不確定性,可能會因各種因素的變化而變化(其中許多因素超出公司的控制)。公司並不承擔公開更新任何前瞻性陳述的義務,無論是由於新信息、未來演示還是其他情況,除非法律要求。
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INVESTOR CONTACT:
Jenene Thomas, JTC Team, LLC
NVNO@jtcir.com
(908) 824-0775
投資者聯繫方式:
Jenene Thomas, JTC團隊,有限責任公司
NVNO@jtcir.com
(908) 824-0775
SOURCE: enVVeno Medical Corporation
來源:enVVeno Medical Corporation
譯文內容由第三人軟體翻譯。