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Набор скоро начнётся NCT06081153

Mechanistic Clinical Trial of PCSK9 Inhibition for AAA

Ранняя фаза I С лечением Abdominal Aortic Aneurysm

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: Evolocumab, Placebo.
Кому может быть актуально
Состояния в реестре: Abdominal Aortic Aneurysm. Базовые параметры: от 18 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
США
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →

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Официальное название

A Randomized, Placebo-Controlled Mechanistic Clinical Trial of PCSK9 Inhibition With Evolocumab in Patients Undergoing Open Abdominal Aortic Aneurysm Repair

Обзор

The goal of this mechanistic clinical trial is to assess whether lowering the low-density lipoprotein cholesterol (LDL-C) levels in the blood with the injections of the medication evolocumab will have any effect on the tissue or cells of patients with abdominal aortic aneurysm (AAA). Researchers will compare participants receiving evolocumab injections to participants receiving placebo injections to see how the tissue and cells of the aorta are affected by changes in LDL-C levels.

Подробное описание

After being informed about the study and its potential risks, all patients giving informed consent will undergo a baseline visit and be randomized to received either evolocumab 140mg subcutaneously or placebo. This baseline visit includes a vital signs assessment, laboratory tests, medical history and medication review, a pregnancy test (if applicable), and training on how to perform drug injections. Participants will receive 3 doses/autoinjectors of study drug or placebo and be instructed to perform injections every 14 days starting 5 weeks prior to their scheduled AAA repair. If the baseline assessment occurs 5 weeks prior to their scheduled AAA, the first injection will be performed during this visit. Participants will have the option of coming back to the site for injections 2 and 3 or perform these injections at home under telehealth supervision. At the time of open AAA repair, participants will repeat laboratory tests and have a sample of aneurysm tissue taken. Participants will then have a follow up phone call 4 weeks after AAA repair to assess for any adverse events. At the conclusion of the study investigators will examine gene expression and protein levels in the aortic tissue to determine the impact of LDL-C lowering with evolocumab.

Вмешательства

  • Препарат Evolocumab
    See arm description.
  • Препарат Placebo
    See arm description.

Первичные конечные точки

  • Interleukin (IL)-6 in myeloid derived monocytes/macrophages from in AAA tissue [Срок оценки: AAA Repair (Week 5)]
Вторичные конечные точки (3)
  • Matrix metalloproteinase (MMP)-9 in myeloid derived monocytes/macrophages from in AAA tissue [Срок оценки: AAA Repair (Week 5)]
  • Infiltrating immune cell composition and their activation/inflammatory states in AAA tissue [Срок оценки: AAA Repair (Week 5)]
  • Smooth muscle composition of AAA tissue [Срок оценки: AAA Repair (Week 5)]

Критерии участия

Критерии включения

  • Abdominal aortic aneurysm (AAA) requiring open surgical repair
  • Age > 18
  • Provision of signed and dated informed consent form
  • Stated willingness to comply with all study procedures and availability for the duration of the study

Критерии исключения

  • Prior use of a PCSK9 inhibitor (evolocumab, alirocumab, inclisiran) within 6 months of the baseline visit
  • LDL-C < 40 mg/dL (within 3 months of baseline visit)
  • Known allergy to PCSK9 inhibitor
  • Aortic dissection
  • Vascular connective tissue disorders
  • Type I-III or V Thoraco-abdominal Aortic Aneurysm
  • Vasculitis or inflammatory aneurysm
  • Pregnant or lactating women
  • Poorly controlled diabetes (A1C > 10%)
  • Chronic kidney disease Stage 4/5 or End Stage Renal Disease (ESRD) on hemodialysis (HD)
  • Liver Disease (alanine transaminase \[ALT\] or aspartate aminotransferase \[ALT\] > 3.0 x upper limits of normal) (within 3 months of baseline visit)
  • Known latex or naturally rubber allergy
  • Treatment with another investigational product within 30 days or 5 half-lives of the investigation drug before consent (whichever is longer) that would have an impact on endpoints associated with this trial.
  • Any other condition that the Investigator feels prohibits participants' ability to comply with study or follow up.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Четверное слепое
Основная цель
Другое

Центры проведения

США · 1 центр
  • Hospital of the University of Pennsylvania — Philadelphia

Идентификаторы

NCT: NCT06081153 · 852428 · R01HL166991

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗