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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

EnVVeno 医疗成功完成预临床GLP研究的最后一波植入。
Accesswire ·  12/16 05:50

Successful Completion of All Planned Implants in GLP Study

成功完成GLP研究中所有计划的植入

enVVe Delivery System Demonstrates Consistent Performance

enVVe输送系统展示了一致的性能

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申请的时间表,等待GLP研究结果

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.

加利福尼亚州欧文 / ACCESSWIRE / 2024年12月16日 / enVVeno医疗公司(纳斯达克:NVNO)("enVVeno"或"公司"),一家为静脉疾病治疗设定新护理标准的公司,今天宣布为其六个月的临床前GLP研究成功完成了短期受试者的最后一波植入。

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研究中所有计划的植入,包括长期和短期受试者,完成了研究的关键阶段。随访期从第一波植入开始,按计划持续进行。待GLP研究成功完成,公司预计将在2025年中期向FDA提交其IDE申请。该申请若获得批准,将允许公司启动enVVe的关键临床试验。

"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."

“随着enVVe GLP研究中所有计划植入的成功完成,我们达成了2024年的最后一个里程碑,”enVVeno医疗公司首席执行官罗伯特·伯曼表示。“我们增强的enVVe压缩和输送系统在整个研究中表现非常出色,准备进行关键试验。我们将继续监测enVVe瓣膜在研究余下部分的表现,若数据和病理结果成功,应能在2025年中期按时提交IDE申请。我们始终专注于成为重度深静脉CVI患者外科和非外科替代静脉瓣市场的确立领导者。”

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.

重度深静脉慢性静脉功能不全(CVI)是一种致残性疾病,通常由腿部深静脉中的血栓(深静脉血栓形成或DVT)引起。当腿部静脉内的瓣膜失效时,血液朝错误的方向流动并在小腿内淤积,导致腿部静脉内的压力增加(静脉高血压)。重度CVI的症状包括腿部肿胀、疼痛、水肿,在最严重的情况下,出现称为静脉性溃疡的复发性开放性伤口。这种疾病可以严重影响日常功能,例如睡眠、洗澡、穿衣和行走,并且已知会导致高发的抑郁和焦虑。目前没有有效的治疗方法可以解决由瓣膜功能不全引起的深静脉系统的重度CVI。估计CVI每年给美国医疗系统造成超过40亿美元的费用。

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.

公司的主打产品是VenoValve,这是一种潜在的首创外科手术更换静脉瓣,适用于严重深静脉慢性静脉功能不全(CVI)患者。在11月, 公司向美国食品和药物管理局提交了一份PMA申请,寻求在美国市场和销售VenoValve的批准。公司估计,美国每年大约有250万名潜在新患者可能成为VenoValve的候选者。公司还在开发enVVe,这是一种基于导管的下一代更换静脉瓣,可能吸引更大市场的患者和医生。

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.

从明年初开始,公司将开始实施其策略,将VenoValve的开发阶段转变为商业实体,同时完成enVVe的必要非临床和GLP测试,以为其IDE申请做好准备。

About enVVeno Medical Corporation

关于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(纳斯达克:NVNO)是一家位于加利福尼亚尔湾的晚期临床阶段医疗器械公司,专注于推动创新生物假体(基于组织的)解决方案,以改善静脉疾病治疗的标准。从的主打产品VenoValve是一种首创的外科手术更换静脉瓣,旨在治疗深静脉慢性静脉功能不全(CVI)。公司还在开发一种用于治疗深静脉CVI的非外科、基于导管的更换静脉瓣,称为enVVe。CVI发生在腿部静脉内的瓣膜受到损害时,导致血液反向流动(返流)、血液在小腿处聚集、腿部静脉压力增加(静脉高血压),在严重情况下会出现难以愈合的静脉溃疡,并且变得慢性。VenoValve和enVVe都设计为单向瓣膜,帮助推动血液上行到腿部,并返回心脏和肺部。VenoValve目前在SAVVE美国关键研究中进行评估,公司正在进行最终测试,以寻求对enVVe关键试验的批准。

Cautionary Note on Forward-Looking Statements

关于前瞻性声明的警示说明

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.

本新闻稿及enVVeno Medical Corporation(“公司”)的股东、董事、员工、代表和合伙人相关的任何声明含有或可能含有在1995年《私人证券诉讼改革法》意义上的某些“前瞻性陈述”。这些前瞻性陈述涉及重大风险和不确定性。这些陈述可能包括但不限于使用“项目”、“可能”、“将”、“可以”、“会”、“应该”、“相信”、“期望”、“预期”、“估计”、“打算”、“计划”、“潜在”或类似表达的陈述。这些陈述基于公司管理层当前的信念和期望,并受到重大风险和不确定性的制约,包括在公司向证券交易委员会的文件中详细列出的风险。实际结果和时机可能与前瞻性陈述中所设定或暗示的内容存在显著差异。前瞻性陈述涉及某些风险和不确定性,可能会因各种因素的变化而变化(其中许多因素超出公司的控制)。公司并不承担公开更新任何前瞻性陈述的义务,无论是由于新信息、未来演示还是其他情况,除非法律要求。

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INVESTOR CONTACT:
Jenene Thomas, JTC Team, LLC
NVNO@jtcir.com
(908) 824-0775

投资者联系方式:
Jenene Thomas, JTC团队,有限责任公司
NVNO@jtcir.com
(908) 824-0775

SOURCE: enVVeno Medical Corporation

来源:enVVeno Medical Corporation


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