- ICH GCP
- Реестр клинических исследований США
- Клиническое испытание NCT07932730
Disulfiram for Preventing Treatment Complications in Patients Undergoing CAR T-cell Therapy for Relapsed or Refractory Diffuse Large B-cell Lymphoma
A Single Center, Phase I/II Study of Disulfiram for the Prevention of Immunotoxicity in Patients Undergoing CAR T-Cell Therapy
This phase I/II trial tests the safety, best dose, and effectiveness of disulfiram for preventing treatment complications in patients with large B-cell lymphoma that has come back after a period of improvement (relapsed) or that does not respond to treatment (refractory) and who are undergoing chimeric antigen receptor (CAR) T-cell therapy. Two major complications of CAR T-cell therapy include cytokine release syndrome (CRS) and immune effector cell-associated neurotoxicity syndrome (ICANS). CRS results from inflammation in the body when the immune system responds too aggressively to the modified T cells working to attack cancer cells. ICANS is inflammation of the brain or nerves. CRS is most often a prelude to ICANS, and both of these toxicities currently require immunosuppression for treatment, which can inhibit CAR T-cell response. Disulfiram has been found to impact several biologic pathways that cause CRS. Disulfiram may be safe and effective for reducing the incidence and severity of reactions to CAR T-cell therapy without inhibiting CAR T-cell response.
Обзор исследования
Статус
Условия
Тип исследования
Регистрация (Оцененный)
Фаза
- Фаза 2
- Фаза 1
Контакты и местонахождение
Контакты исследования
- Имя: Tracey Churay
- Номер телефона: 1-800-865-1125
- Электронная почта: tchuray@umich.edu
Места учебы
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Michigan
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Ann Arbor, Michigan, Соединенные Штаты, 48109
- University of Michigan Rogel Cancer Center
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Контакт:
- Tracey Churay
- Номер телефона: 800-865-1125
- Электронная почта: tchuray@umich.edu
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Главный следователь:
- Marcus Geer
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Критерии участия
Критерии приемлемости
Возраст, подходящий для обучения
Принимает здоровых добровольцев
Полы, имеющие право на обучение
Описание
Inclusion Criteria:
- Histologic diagnosis of relapsed/refractory large B-cell lymphoma
- >= 18 years of age at the time of signing informed consent (ICF)
- Understands and voluntarily signs the ICF prior to conduct of any study-related assessments or procedures
- Willing to adhere to the study visit schedule and other protocol requirements
- Willing/able to abstain from any drug/substance at risk for reaction with disulfiram for the duration of treatment
- Eastern Cooperative Oncology Group (ECOG) performance status =< 2
- Eligible for therapy with axicabtagene ciloleucel per institutional criteria
- Confirmation of a manufactured CAR T-cell product within clinical specifications for axicabtagene ciloleucel
- Females and males of childbearing potential must be willing to use effective methods of contraception from the time of informed consent until 12 months (female) or 4 months (males with female partners of reproductive potential) after the cyclophosphamide infusion
- Willingness to consent / co-enroll on the University of Michigan cellular therapy long-term follow-up study - HUM00043287 (UMCC2001-0234)
Exclusion Criteria:
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Serious or uncontrolled infection defined as not having cleared infection despite being on appropriate antimicrobial therapy for 5 days would be excluded. Also any infection which, in the opinion of the investigator, places the patient at an unacceptable risk for treatment-related complications, could impede the ability to safely administer therapy, or could interfere with evaluation of study intervention
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Active hepatitis B or C (latent hepatitis B will not be excluded), or HIV. Entecavir prophylaxis can be used for latent hepatitis B. A patient's viral load must be undetectable per quantitative polymerase chain reaction (PCR) and/or nucleic acid testing at screening
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Total bilirubin of >= 1.5 x upper limit of normal (ULN) unless attributed to Gilbert's syndrome or underlying primary malignancy. Patients with Gilbert syndrome or underlying primary malignancy involving the liver with total bilirubin >= 2.5 x ULN (or absolute total bilirubin >= 3 mg/dL) should be excluded. Aspartate aminotransferase (AST): >= 2.5 x ULN, alanine aminotransferase (ALT): >= 2.5 x ULN
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Active concurrent autoimmune disease requiring systemic immunosuppression
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Active primary or secondary central nervous system (CNS) lymphoma
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Active clinically relevant central nervous system disease including but not limited to:
- Seizures/Epilepsy
- Stroke or unstable neurologic deficits within the past 12 months prior to enrollment
- Cerebral edema
- Aphasia
- Severe brain injury
- Cerebellar disease
- Documented history of dementia as confirmed by neuropsychiatric testing
- Parkinson's disease
- Psychosis
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Any other significant medical condition (including neurological or psychiatric) which, in the opinion of the investigator, places the participant at an unacceptable risk for treatment-related complications, could interfere with the successful or safe delivery of therapy, or could interfere with evaluation of study intervention or interpretation of participant safety or study results. Including but not limited to:
- Diabetes with associated autonomic dysfunction
- Uncontrolled Hypothyroidism
- Chronic or acute nephritis
- Hepatic cirrhosis/insufficiency
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Pregnant or nursing females
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Current or previous treatment with any other agents explicitly for prophylaxis of CRS or ICANS, including corticosteroids and investigational agents during the study enrollment period. Corticosteroids given for disease treatment should have a washout of at least 5 half-lives prior to cell infusion. Use of prophylactic antiseizure medications is not contraindicated
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History of, or a concurrent, clinically significant illness, medical condition or laboratory abnormality that, in the investigator's opinion, could affect the conduct of the study
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Concurrent use of prohibited medications or substances at risk of precipitating a disulfiram reaction
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Hypersensitivity to disulfiram or to other thiuram derivatives used in pesticides and rubber vulcanization
Учебный план
Как устроено исследование?
Детали дизайна
- Основная цель: Поддерживающая терапия
- Распределение: Н/Д
- Интервенционная модель: Одногрупповое задание
- Маскировка: Нет (открытая этикетка)
Оружие и интервенции
Группа участников / Армия |
Вмешательство/лечение |
|---|---|
|
Экспериментальный: Supportive care (disulfiram)
Patients receive disulfiram PO QD on days -5 to +21. Patients receive cyclophosphamide IV and fludarabine IV on days -5 to -3 and then receive axi-cel IV on day 0. Patients also undergo CT or PET/CT at screening and follow-up and undergo collection of blood samples throughout the trial. |
Given IV
Другие имена:
Undergo collection of blood samples
Другие имена:
Undergo CT or PET/CT
Другие имена:
Undergo PET/CT
Другие имена:
Given IV
Другие имена:
Given IV
Другие имена:
Given PO
Другие имена:
|
Что измеряет исследование?
Первичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
Incidence of dose-limiting toxicities
Временное ограничение: Within day +35 post-chimeric antigen receptor (CAR) T-cell therapy
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At the end of the trial, will report number of patients assigned to each dose, as well as the number of patients experiencing toxicity at each dose. |
Within day +35 post-chimeric antigen receptor (CAR) T-cell therapy
|
|
Proportion of patients that are alive and free from grade 2-4 cytokine release syndrome (CRS) with no intervening treatment of CRS
Временное ограничение: Through day +28 post-CAR T-cell therapy
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At the end of the trial, will report number of patients assigned to each dose, as well as the number of patients experiencing efficacy outcomes at each dose. |
Through day +28 post-CAR T-cell therapy
|
Вторичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
Incidence of grade 2-4 CRS
Временное ограничение: By day +28 post-CAR T-cell therapy
|
The occurrence of severe CRS will be considered binary, and the rate will be defined as number of patients with severe CRS divided by the number of evaluable patients. The rate will be reported along with the 95% exact binomial confidence interval. |
By day +28 post-CAR T-cell therapy
|
|
Incidence of all-grade CRS
Временное ограничение: By day +28 post-CAR T-cell therapy
|
The occurrence of CRS will be considered binary, and the rate will be defined as number of patients with CRS divided by the number of evaluable patients. The rate will be reported along with the 95% exact binomial confidence interval. |
By day +28 post-CAR T-cell therapy
|
|
Incidence of all-grade immune effector cell associated neurotoxicity syndrome (ICANS)
Временное ограничение: By day +28 post-CAR T-cell therapy
|
The occurrence of severe ICANS will be considered binary and the rate will be defined as number of patients with severe ICANS divided by the number of evaluable patients. The rate will be reported along with the 95% exact binomial confidence interval. |
By day +28 post-CAR T-cell therapy
|
|
Incidence of disulfiram-related grade 2 to 5 non-hematologic toxicity
Временное ограничение: By day +28 post-CAR T-cell therapy
|
Will be assessed by Common Terminology Criteria for Adverse Events, version 5.0. The occurrence of drug related grade 2-5 non-hematologic toxicity with at least a 'possible' attribution to disulfiram will be considered binary, and the rate will be defined as number of patients experiencing toxicity divided by the number of evaluable patients. The rate will be reported along with the 95% exact binomial confidence interval. |
By day +28 post-CAR T-cell therapy
|
Соавторы и исследователи
Следователи
- Главный следователь: Marcus Geer, University of Michigan Rogel Cancer Center
Даты записи исследования
Изучение основных дат
Начало исследования (Оцененный)
Первичное завершение (Оцененный)
Завершение исследования (Оцененный)
Даты регистрации исследования
Первый отправленный
Впервые представлено, что соответствует критериям контроля качества
Первый опубликованный (Действительный)
Обновления учебных записей
Последнее опубликованное обновление (Действительный)
Последнее отправленное обновление, отвечающее критериям контроля качества
Последняя проверка
Дополнительная информация
Термины, связанные с этим исследованием
Дополнительные соответствующие термины MeSH
- Новообразования
- Заболевания иммунной системы
- Новообразования по гистологическому типу
- Лимфатические заболевания
- Лимфопролиферативные заболевания
- Иммунопролиферативные заболевания
- Лимфома, неходжкинская
- Лимфома, В-клеточная
- Лимфома
- Гемики и лимфатические заболевания
- Лимфома, крупная В-клеточная, диффузная
- Средние соединения
- Органические химические вещества
- Следственные методы
- Клинические лабораторные методы
- Диагностические методы и процедуры
- Диагноз
- Углеводороды
- Кислоты, ациклические
- Карбоновые кислоты
- Химические методы, аналитические
- Анализ спектра
- Фосфорамид горчицы
- Азотные соединения горчицы
- Горчичные соединения
- Углеводороды, галогенированные
- Фосфорамиды
- Соединения органофосфора
- Сульфиды
- Карбаматы
- Ditiocarb
- Тиокарбаматы
- Дисульфиды
- Циклофосфамид
- Дисульфирам
- Обработка образца
- Магнитно -резонансная спектроскопия
- флударабин
- Аксимабтагеновая цилолеузель
Другие идентификационные номера исследования
- UMCC 2025.132
- NCI-2026-05448 (Идентификатор реестра: CTRP (Clinical Trial Reporting Program))
- HUM00287270 (Другой идентификатор: University of Michigan Rogel Cancer Center)
Планирование данных отдельных участников (IPD)
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Информация о лекарствах и устройствах, исследовательские документы
Изучает лекарственный продукт, регулируемый FDA США.
Изучает продукт устройства, регулируемый Управлением по санитарному надзору за качеством пищевых продуктов и медикаментов США.
продукт, произведенный в США и экспортированный из США.
Эта информация была получена непосредственно с веб-сайта clinicaltrials.gov без каких-либо изменений. Если у вас есть запросы на изменение, удаление или обновление сведений об исследовании, обращайтесь по адресу register@clinicaltrials.gov. Как только изменение будет реализовано на clinicaltrials.gov, оно будет автоматически обновлено и на нашем веб-сайте. .