A Novel Endovascular Approach to Remove Atherosclerotic Plaque Lesions In Situ

一种原位去除动脉粥样硬化斑块病变的新型血管内方法

• 批准号: 10577344
• 负责人: Melina Rae Kibbe
• 金额: $ 63.56万
• 依托单位: UNIVERSITY OF VIRGINIA
• 依托单位国家: 美国
• 财政年份: 2019
• 资助国家: 美国
• 起止时间: 2019-01-01 至 2024-12-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/10577344
• 关键词: Affect; Aneurysm; Angiography; Animal Model; Area; Arterial Fatty Streak; Arteries; Atherosclerosis; Balloon Angioplasty; Balloon Occlusion; Blood; Blood Vessels; Calcium; Cardiovascular Diseases; Carotid Arteries; Catheters; Cause of Death; Cells; Clinical; Coagulation Process; Collagen; Complement Activation; Custom; Data; Development; Digestion; Dilatation - action; Dissection; Distal; Elastases; Embolism; Endothelium; FDA approved; Family suidae; Fibrin; Goals; Health; Human; Hyperplasia; Immunohistochemistry; In Situ; In Situ Lesion; Individual; Inflammation; Inflammatory; Intervention; Knowledge; Lead; Life; Lipids; Longitudinal Studies; Mechanics; Metals; Methods; Mission; Outcome Measure; Persons; Phase I Clinical Trials; Platelet aggregation; Procedures; Proteoglycan; Research Personnel; Safety; Secondary to; Smooth Muscle Myocytes; Sonication; Stents; Superficial Femoral Artery; Techniques; Technology; Testing; Thick; Thrombosis; Time; Trauma; Tumor Debulking; Ultrasonography; United States; United States National Institutes of Health; Vasomotor; base; clinically relevant; conventional therapy; disability; efficacy study; first-in-human; heat injury; iliac artery; improved outcome; in vivo Model; innovation; medical specialties; multidisciplinary; new technology; non-compliance; novel; optimal treatments; porcine model; pre-clinical; restenosis; safety study; sex; systemic inflammatory response; targeted agent; time use; ultrasound

SUMMARY Cardiovascular disease secondary to atherosclerosis is the leading cause of death in the United States. Current percutaneous vascular interventions that treat severe atherosclerosis require inflation of a balloon with or without deployment of a rigid, non-compliant metal stent. Yet, this technique fails to remove the atherosclerotic plaque burden and causes mechanical trauma to the arterial wall, resulting in significant restenosis rates. FDA-approved plaque debulking technologies do exist and are used in the clinical arena. However, to debulk the plaque, each of these therapies induces some form of mechanical or thermal injury to the vessel wall, which ultimately stimulates the development of neointimal hyperplasia and results in significant arterial restenosis. Therefore, the goal of this study is to develop a novel endovascular technology to reduce atherosclerotic plaque burden without inducing thermal or mechanical trauma to the arterial wall. Our paradigm-shifting technology is based on a safe method of digesting atherosclerotic plaque in situ through the use of a double occlusion balloon catheter, sonication wire, and a highly customized solution tailored to safely digest atherosclerotic plaque. Given that most atherosclerotic plaques are composed of collagen, fibrin, lipids, proteoglycans, inflammatory cells, smooth muscle cells, and calcium, we hypothesize that a digestion solution containing agents that target these plaque components will dissolve and digest the plaque in situ within a clinically relevant time frame. Avoidance of the use of elastases in our solution limits digestion of the plaque to the elastic lamina. With our multidisciplinary team of investigators, we have already demonstrated the feasibility and initial safety of our approach through preliminary data. We have demonstrated effective digestion of excised human carotid artery atherosclerotic plaques as well as the plaque inside intact human superficial femoral arteries. We have evaluated our approach in a non-atherosclerotic porcine model in vivo and showed that our therapy did not injure the arterial wall, was limited to the internal elastic lamina, and did not result in dissections or aneurysm formation, suggesting that our therapy is safe. Lastly, we evaluated our approach in an atherosclerotic porcine model and demonstrated initial efficacy at reducing plaque without inducing thrombosis or aneurysmal degeneration. Given the feasibility and promise of these preliminary data, we believe further scientific exploration and development of this novel technology is warranted and will lead to an innovative clinical therapy for the treatment of atherosclerosis in humans. Thus, the overall objective of this proposal is to robustly evaluate the safety, efficacy, durability, and repeatability of this therapy in a preclinical porcine animal model of atherosclerosis. Successful completion of these studies will directly lead to an FDA application for a first-in-human Phase 1 clinical trial, and is thus highly aligned with the mission of the National Institutes of Health to “enhance health, lengthen life, and reduce illness and disability” through the application of new knowledge.

总结 在美国，继发于动脉粥样硬化的心血管疾病是导致死亡的主要原因。 目前治疗严重动脉粥样硬化的经皮血管介入治疗需要用球囊充胀， 或者不使用刚性的、非顺应性的金属支架。然而，这种技术无法消除 动脉粥样硬化斑块负担并对动脉壁造成机械创伤，导致显著的 再狭窄率。FDA批准的斑块减积技术确实存在并用于临床竞技场。 然而，为了使斑块变小，这些疗法中的每一种都会引起某种形式的机械或热损伤， 血管壁，最终刺激新生内膜增生的发展，并导致显著的 动脉再狭窄因此，本研究的目标是开发一种新型血管内技术， 减少动脉粥样硬化斑块负荷，而不会对动脉造成热损伤或机械损伤 墙我们的范式转换技术是基于一种安全的原位消化动脉粥样硬化斑块的方法 通过使用双闭塞球囊导管、超声导丝和高度定制的解决方案， 能够安全消化动脉粥样硬化斑块考虑到大多数动脉粥样硬化斑块是由 胶原蛋白、纤维蛋白、脂质、蛋白多糖、炎症细胞、平滑肌细胞和钙，我们假设 含有靶向这些菌斑组分的试剂的消化溶液将溶解， 在临床相关的时间范围内原位消化斑块。在我们的研究中避免使用弹性蛋白酶 溶液将斑块的消化限制在弹性膜上。通过我们的多学科研究团队，我们 已经通过初步数据证明了我们方法的可行性和初步安全性。我们有 证实了有效消化切除的人颈动脉粥样硬化斑块以及斑块 完整的人类股浅动脉内我们已经在非动脉粥样硬化性 猪体内模型，并表明我们的治疗不损伤动脉壁，仅限于内部 弹性膜，并没有导致夹层或动脉瘤形成，这表明我们的治疗是安全的。 最后，我们在动脉粥样硬化猪模型中评估了我们的方法，并证明了在 减少斑块，而不诱导血栓形成或囊性变性。考虑到可行性和前景， 根据这些初步数据，我们相信，进一步的科学探索和发展这项新技术， 并将导致用于治疗人类动脉粥样硬化的创新临床疗法。因此，在本发明中， 本提案的总体目标是对安全性、有效性、耐久性和 在动脉粥样硬化的临床前猪动物模型中的这种疗法的可重复性。成功 这些研究的完成将直接导致FDA申请进行首次人体I期临床试验， 因此与美国国立卫生研究院的使命“增强健康，延长寿命， 减少疾病和残疾”。