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Идёт набор NCT04925492

PET Imaging of Vaso-Occlusive Crisis (VOC) in SCD

Фаза I С лечением Sickle Cell Disease

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: Positron Emission Tomography, Cu-64]-LLP2A.
Кому может быть актуально
Состояния в реестре: Sickle Cell Disease. 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
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Официальное название

Positron Emission Tomography (PET) Imaging of Vaso-occlusive Crisis(VOC) in Sickle Cell Disease (SCD).

Обзор

The purpose of this study is to find objective biomarkers of vaso-occlusion (blood vessel blockage) in people with SCD. Using information from earlier studies and work being done, researchers have developed a strategy to image VOC, using positron emission tomography (PET). The ability to see and measure VOC in SCD patients can help patient care, by showing when and how a VOC is occurring or going to occur. Studying this method will also help in future drug research, as it will allow researchers to deliver promising new medications that target hyper-adhesion and sickling in people with SCD.

Подробное описание

The purpose of this study is to find objective biomarkers of vaso-occlusion (blood vessel blockage) in people with Sickle Cell Disease(SCD). Using information from earlier studies, and work being done at Washington University, a strategy to image vaso-occulusive crisis (VOC) has been developed, using positron emission tomography (PET) for anatomical localization only. 64Cu-LLP2A is the radio tracer used for the study.

Aim: To develop quantitative PET imaging of VOC in patients with SCD. The researchers hypothesize that the radio tracer 64Cu-LLP2A uptake increases proportionally to the intensity of pain in patients with VOC, compared to baseline values. This increase in uptake will be assessed focally in areas of pain as well as globally to reflect heightened systemic inflammation.

Primary and secondary study endpoint: The overarching hypothesis of this study is that PET tracer uptake of intensity of 64Cu-LLP2A is a real time, quantitative measure of hyper adhesion in VOC.

Вмешательства

  • Лучевая терапия Positron Emission Tomography
    An imaging method that uses radiotracers to view changes in the metabolic process.
  • Препарат Cu-64]-LLP2A
    A radioactive tracer used in PET imaging.

Первичные конечные точки

  • Change in PET tracer uptake in VOC [Срок оценки: Up to five years from first assessment depending on when VOC occurs.]
  • Association of PET tracer uptake with intensity of pain in VOC [Срок оценки: 2 hours during an assessment while in VOC.]
  • Association of PET tracer uptake with clinical VOC markers [Срок оценки: Up to the length of a hospital visit for treatment of VOC. On average, about 5 days.]

Критерии участия

Критерии включения

  • Have a confirmed diagnosis of SCD (HbSS, SC, S/β-thalassemia, SD, SE, SO) by hemoglobin electrophoresis/High Performance Liquid Chromatography (HPLC)
  • Aged 18 and above
  • Ability to understand and provide informed consent.
  • If receiving hydroxyurea or L-glutamine, crizanlizumab, voxelotor or erythropoietin stimulating agents, must have been receiving the drug for at least 12 weeks prior to screening and plan to continue taking the drug at the same dose and schedule during the study
  • Experienced at least 2 VOCs leading to healthcare visit within the 12 months prior to screening visit as determined by medical history.

Критерии исключения

  • Active malignancy
  • Current pregnancy or breast feeding
  • Participating in a chronic transfusion program (pre-planned series of transfusions for prophylactic purposes) and/or planning on undergoing an exchange transfusion during the duration of the study; episodic transfusion in response to worsened anemia or VOC is permitted
  • Received active treatment on another investigational trial within 30 days (or 5 half-lives of that agent, whichever is greater) prior to screening visit or plans to participate in another investigational drug trial

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

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Нерандомизированное
Модель
Последовательный дизайн
Маскирование
Открытое
Основная цель
Скрининг

Центры проведения

США · 1 центр
  • UPMC — Pittsburgh

Идентификаторы

NCT: NCT04925492 · STUDY20020135 · R01HL154629

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗