- ICH GCP
- Реестр клинических исследований США
- Клиническое испытание NCT06523556
Аксатилимаб с азацитидином или без него для лечения пациентов с миелопролиферативными новообразованиями поздней фазы, перекрытием миелопролиферативных новообразований/миелодиспластического синдрома или хроническим миеломоноцитарным лейкозом высокого риска
Исследование фазы 1b/2 аксатилимаба (SNDX-6352) + азацитидина (AZA) на поздней стадии МПН, совпадения МПН/МДС или ХММЛ высокого риска
This phase Ib/II trial tests the best dose of axatilimab and effectiveness of axatilimab with or without azacitidine for the treatment of patients with advanced phase myeloproliferative neoplasms (MPN), myeloproliferative neoplasm/myelodysplastic syndrome (MPN/MDS) overlap or high risk chronic myelomonocytic leukemia (CMML). Axatilimab is an antibody that is cloned from a single white blood cell that is known to be able to recognize cancer cells and block a protein on the surface of the white blood cells that may be involved in cancer cell growth. By blocking the proteins, this may slow or halt the growth of the cancer. Azacitidine is in a class of medications called antimetabolites. It works by stopping or slowing the growth of cancer cells. Giving axatilimab with or without azacitidine may be safe and effective in treating patients with advanced phase MPN, MPN/MDS overlap or high risk CMML.
Обзор исследования
Статус
Условия
- Хронический миеломоноцитарный лейкоз
- Рефрактерный хронический миеломоноцитарный лейкоз
- Миелодиспластическое/миелопролиферативное новообразование
- Рецидивирующее миелодиспластическое/миелопролиферативное новообразование
- Атипичный хронический миелоидный лейкоз
- Рецидивирующее миелопролиферативное новообразование
- Рефрактерное миелодиспластическое/миелопролиферативное новообразование
- Рефрактерное миелопролиферативное новообразование
Подробное описание
PRIMARY OBJECTIVES:
I. To determine the recommended phase 2 dose (RP2D) of axatilimab in relapsed or refractory patients with advanced phase MPN, MPN/MDS overlap or high-risk CMML.
II. To evaluate the overall response rate of axatilimab + azacitidine (AZA) in newly diagnosed patients with advanced phase MPN, MPN/MDS overlap or high-risk CMML using Savona response criteria.
SECONDARY OBJECTIVES:
I. Determine the safety and tolerability of axatilimab + azacitidine combination therapy in those with newly diagnosed advanced phase MPN, MPN/MDS overlap or high-risk CMML.
II. Determine the quality of life in patients receiving axatilimab + AZA using a Modified Myeloproliferative Neoplasm Symptom Assessment Form (MPNSAF).
III. Determine the effect of axatilimab + azacitidine on symptom relief which will be measured by transfusion burden (platelet and/or packed red blood cell), time in hospital, and immune related side effects specifically reactivation of tuberculosis (TB), infusion-related reactions, hepatotoxicity, pneumonia, pyrexia, sepsis, shortness of breath (SBO), hemoptysis, periorbital edema, fatigue, and pancreatitis.
EXPLORATORY OBJECTIVES:
I. To assess the pharmacokinetics of axatilimab in combination with AZA. II. To describe the prevalence and trajectories of patients' physical activity during treatment.
III. To perform detailed correlative studies related to genetic, biochemical, and immunologic changes that occur with axatilimab in combination with AZA.
OUTLINE: This is a phase I, dose-escalation study of axatilimab followed by a phase II study.
PHASE I: Patients receive axatilimab intravenously (IV) over 30 minutes on days 1 and 15 of each cycle. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. At time of phase Ib completion, patients with clinical improvement may transition to phase II. Patients undergo bone marrow biopsy and aspiration and blood sample collection throughout the study.
PHASE II: Patients receive axatilimab IV over 30 minutes on days 1 and 15 and azacitidine IV over 10-40 minutes or subcutaneously (SC) on days 1-7 of each cycle. Cycles repeat every 28 days for up to 4 cycles in the absence of disease progression or unacceptable toxicity. Patients who achieve partial response (PR) or better may continue for up to 24 total cycles. Patients who achieve less than PR receive 2 additional cycles and, if PR or better is achieved, may complete up to 24 total cycles. Patients undergo bone marrow biopsy and aspiration and blood sample collection throughout the study.
After completion of study treatment, patients are followed up at 30 days and then every 6 months for up to 24 months after last dose of study medication.
Тип исследования
Регистрация (Оцененный)
Фаза
- Фаза 2
- Фаза 1
Контакты и местонахождение
Контакты исследования
- Имя: The Ohio State University Comprehensive Cancer Center
- Номер телефона: 800-293-5066
- Электронная почта: OSUCCCClinicaltrials@osumc.edu
Места учебы
-
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Ohio
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Columbus, Ohio, Соединенные Штаты, 43210
- Рекрутинг
- Ohio State University Comprehensive Cancer Center
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Контакт:
- Uma M. Borate
- Номер телефона: 614-293-3316
- Электронная почта: Uma.Borate@osumc.edu
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Главный следователь:
- Uma M. Borate
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Oregon
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Portland, Oregon, Соединенные Штаты, 97239
- Рекрутинг
- Oregon Health & Science University
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Контакт:
- Knight Cancer Institute Clinical Trials
- Номер телефона: 503-494-1080
- Электронная почта: trials@ohsu.edu
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Контакт:
- Ted Braun, MD, PhD
- Номер телефона: 503-494-1080
- Электронная почта: braunt@ohsu.edu
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Главный следователь:
- Ted Braun, MD, PhD
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-
Критерии участия
Критерии приемлемости
Возраст, подходящий для обучения
Принимает здоровых добровольцев
Полы, имеющие право на обучение
Описание
Inclusion Criteria:
-
Signed informed consent must be obtained prior to participation in the study
-
Age ≥ 18 years at the date of signing the informed consent form (ICF)
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Morphologically confirmed diagnosis of the following based on 2016 World Health Organization (WHO) classification (Arber et al 2016): Phase 1b, patients with relapsed or refractory of any of the following; phase 2, patients with newly diagnosed of any of the following:
- Chronic myelomonocytic leukemia (CMML), classified as intermediate-2, OR high-risk per the CMML Specific Prognostic Scoring System (CPSS) Molecular Model
- Atypical chronic myelocytic leukemia (aCML)
- MDS/MPN unclassified (MDS/MPN-U)
- Myeloproliferative neoplasm accelerated phase (MPN-AP)
- MPN-AP requires a previous diagnosis of polycythemia vera (PV), essential thrombocythemia (ET), or primary myelofibrosis (PMF) with intermediate-2 or high risk disease according to International Prostate Symptom Score (IPSS) as well as progression on or failure to respond to at least one line of therapy.
- Myelodysplastic syndrome/myeloproliferative neoplasm with ring sideroblasts and thrombocytosis (MDS/MPN-RS-T) or MDS/MPN with SF3B1 mutation and thrombocytosis (MDS/MPN-SF3B1-T).
- Not suitable for immediate myeloablative/intensive chemotherapy based on investigator assessment of age, comorbidities, local guidelines, institutional practice (any or all of these)
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PHASE Ib (RELAPSE [R]/ REFRACTORY [R]): Relapse/refractory patients who have received at least two cycles of disease directed therapy (prior therapies can include hypomethylating agents [HMAs], HMA combination therapies, and other disease directed therapies)
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PHASE II (NEWLY DIAGNOSED PHASE): Newly diagnosed patients without prior treatment, including intensive induction chemotherapy. However, previous treatment with hydroxyurea, ruxolitinib, and/or up to 2 cycles of HMAs (decitabine, azacitidine, oral decitabine [INQOVI]) is permitted
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Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1 or 2
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Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 3 × upper limit of normal (ULN)
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Total bilirubin ≤ 1.5 × ULN (except in the setting of isolated Gilbert syndrome)
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Estimated glomerular filtration rate (eGFR) ≥ 30 mL/min/1.73m^2 (estimation based on Modification of Diet in Renal Disease [MDRD] formula, by local laboratory)
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Patient is able to communicate with the investigator and has the ability to comply with the requirements of the study procedures
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Women of childbearing potential and men, if not surgically sterilized, should use adequate contraception from 14 days prior to study entry and until 90 days after the last follow-up visit. Adequate contraception is defined as using hormonal contraceptives or an intrauterine device combined with at least 1 of the following forms of contraception: a diaphragm or cervical cap, or a condom
Exclusion Criteria:
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Diagnosis of acute myeloid leukemia (AML) including acute promyelocytic leukemia and extra-medullary AML based on WHO 2016 classification (Arber et al 2016)
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Patients who are candidates for myeloablative or intensive chemotherapy treatment or who do not provide consent for this treatment
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History of organ transplant or allogenic hematopoietic stem cell transplant
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Participants with prior malignancy, except:
- Participants with history of adequately treated malignancy for which no anticancer systemic therapy (namely chemotherapy, radiotherapy or surgery) is ongoing or required during the course of the study.
- Participants who are receiving adjuvant therapy such as hormone therapy are eligible. However, participants who developed therapy related neoplasms are not eligible
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Previous known allergy/sensitivity to components of axatilimab
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History of acute or chronic pancreatitis
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History of myositis
Учебный план
Как устроено исследование?
Детали дизайна
- Основная цель: Уход
- Распределение: Нерандомизированный
- Интервенционная модель: Назначение кроссовера
- Маскировка: Нет (открытая этикетка)
Оружие и интервенции
Группа участников / Армия |
Вмешательство/лечение |
|---|---|
|
Экспериментальный: Phase I (Axatilimab)
Patients receive axatilimab IV over 30 minutes on days 1 and 15 of each cycle. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. At time of phase Ib completion, patients with clinical improvement may transition to phase II. Patients undergo bone marrow biopsy and aspiration and blood sample collection throughout the study. |
Undergo blood sample collection
Другие имена:
Given IV
Другие имена:
Undergo bone marrow biopsy and aspiration |
|
Экспериментальный: Phase II (Axatilimab and azacitidine)
Patients receive axatilimab IV over 30 minutes on days 1 and 15 and azacitidine IV over 10-40 minutes or SC on days 1-7 of each cycle. Cycles repeat every 28 days for up to 4 cycles in the absence of disease progression or unacceptable toxicity. Patients who achieve PR or better may continue for up to 24 total cycles. Patients who achieve less than PR receive 2 additional cycles and, if PR or better is achieved, may complete up to 24 total cycles. Patients undergo bone marrow biopsy and aspiration and blood sample collection throughout the study. |
Undergo blood sample collection
Другие имена:
Given IV or SC
Другие имена:
Ancillary study Given IV
Другие имена:
Undergo bone marrow biopsy and aspiration |
Что измеряет исследование?
Первичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
Incidence of dose limiting toxicities
Временное ограничение: Up to 42 days after the first dose of study medication
|
Includes hematologic and non-hematologic toxicities |
Up to 42 days after the first dose of study medication
|
|
Overall response rate
Временное ограничение: Up to 5 years
|
The number of participants whose best response (according to the 2006 International Working Group response criteria) over the efficacy analysis period is a complete response or partial response will be tallied to estimate the overall response rate and provide a 95% exact confidence interval, according to the Clopper-Pearson method. |
Up to 5 years
|
Вторичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
Incidence of adverse events
Временное ограничение: Up to 30 days after end of treatment
|
Adverse events will be tabulated by toxicity grade and relationship with study medication and assessed by Common Terminology Criteria for Adverse Events version 5.0. |
Up to 30 days after end of treatment
|
|
Quality of life measured by Modified Myeloproliferative Neoplasm Symptom Assessment Form (MPNSAF)
Временное ограничение: Up to 5 years
|
Will be assessed in patients receiving axatilimab + azacitidine (AZA) and will be determined using a Modified Myeloproliferative Neoplasm Symptom Assessment Form (MPNSAF) score. The MPNSAF score has a range from 0 to 100 with 100 representing the highest level of symptom severity. Descriptive statistics, means and standard deviations or medians and ranges will be applied to summarize the MPNSAF score. |
Up to 5 years
|
|
Number of platelet transfusions
Временное ограничение: Up to 5 years
|
Will be assessed in patients receiving axatilimab + azacitidine and will be determined by descriptive statistics. |
Up to 5 years
|
|
Number of packed red blood cell transfusions
Временное ограничение: Up to 5 years
|
Will be assessed in patients receiving axatilimab + azacitidine and will be determined by descriptive statistics. |
Up to 5 years
|
|
Time in hospital
Временное ограничение: Up to 5 years
|
Will be assessed in patients receiving axatilimab + azacitidine and will be determined by descriptive statistics. |
Up to 5 years
|
Соавторы и исследователи
Спонсор
Соавторы
Следователи
- Главный следователь: Uma M Borate, MD, Ohio State University Comprehensive Cancer Center
Публикации и полезные ссылки
Полезные ссылки
Даты записи исследования
Изучение основных дат
Начало исследования (Действительный)
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
- Патологические процессы
- Новообразования
- Хроническое заболевание
- Атрибуты болезни
- Новообразования по гистологическому типу
- Гематологические заболевания
- Лейкоз, миелоидный
- Заболевания костного мозга
- Лейкемия
- Патологические состояния, признаки и симптомы
- Гемики и лимфатические заболевания
- Лейкемия, Миеломоноцитарная, Хроническая
- Миелопролиферативные заболевания
- Миелодиспластические-миелопролиферативные заболевания
- Лейкоз, миелоидный, хронический, атипичный, BCR-ABL отрицательный
- Органические химические вещества
- Гетероциклические соединения, 1-кольцо
- Гетероциклические соединения
- Следственные методы
- Клинические лабораторные методы
- Диагностические методы и процедуры
- Диагноз
- Хирургические процедуры, оперативные
- Цитологические методы
- Нуклеиновые кислоты, нуклеотиды и нуклеозиды
- Цитодиагностика
- Цитидин
- Пиримидиновые нуклеозиды
- Пиримидины
- Диагностические методы, хирургический
- Aza Compounds
- Нуклеозиды
- Рибонуклеозиды
- Азацитидин
- Биопсия
- Обработка образца
- Аксулимаб
Другие идентификационные номера исследования
- OSU-23442
- NCI-2024-05515 (Идентификатор реестра: CTRP (Clinical Trial Reporting Program))
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.
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