A Phase 3 Multinational Study of Golidocitinib Versus Investigator's Choice in r/r PTCL (JACKPOT19)
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: Golidocitinib, Chidamide, Gemcitabine.
- Кому может быть актуально
- Состояния в реестре: Peripheral T-cell Lymphoma. 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
- Китай, Тайвань, Таиланд
- 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 Phase 3, Open-Label, Randomized, Multinational Study to Investigate the Anti-tumor Efficacy of Golidocitinib Versus Investigator's Choice in Adult Patients With Relapsed/Refractory Peripheral T-cell Lymphoma
Обзор
This is a phase 3, open-label, randomized, multinational study to evaluate the anti-tumor efficacy of golidocitinib versus investigator's choice in adult patients with relapsed/refractory peripheral T-cell lymphoma (r/r PTCL). This study will treat patients with pathologically confirmed PTCL who have relapsed after or been refractory/intolerant to at least one prior systemic treatment regimen(s).
Вмешательства
- Препарат Golidocitinib
150 mg, orally, once daily, with or without food, in a 21-day cycle - Препарат Chidamide
30 mg, orally, twice a week, with an interval of no less than 3 days in a 21-day cycle - Препарат Gemcitabine
1000 mg/m2, intravenous infusion, administered on Day 1, Day 8 and Day 15 of a 28-day cycle
Первичные конечные точки
- Progression-free survival (PFS) assessed by the Independent Review Committee (IRC) according to Lugano 2014 [Срок оценки: The time from the date of randomization to the date of first progressive disease, death due to any cause whichever occurred first. Approximately 4 years.]
Вторичные конечные точки (1)
- Overall survival (OS) [Срок оценки: The time from randomization to death due to any cause. Approximately 4 years.]
Критерии участия
Критерии включения
- The participants should sign the ICF and be able to comply with the relevant requirements in the ICF and protocol
- Age ≥ 18 years
- ECOG 0-2 score, life expectancy ≥ 12 weeks
- Patients must have histologically confirmed peripheral T-cell lymphoma according to the World Health Organization classification of lymphoma. Eligible subtypes are restricted to: PTCL-not otherwise specified, NOS (PTCL, NOS), Angioimmunoblastic T-cell lymphoma (AITL), anaplastic large-cell lymphoma ALK-positive (ALCL ALK+), anaplastic large-cell lymphoma ALK-negative (ALCL ALK-), Follicular T-cell lymphoma, or PTCL with T-follicular helper (TFH) phenotype (FTCL or PTCL-TFH), Enteropathy-associated T-cell lymphoma (EATL), Monomorphic epitheliotropic intestinal T-cell lymphoma (MEITL), Natural killer/T-cell lymphoma (NK/TCL), Hepatosplenic T-cell lymphoma (HSTCL), Subcutaneous panniculitis-like T-cell lymphoma (SPTCL)
- Progressed on, were refractory to or intolerant to at least one line of prior standard systemic therapies assessed by investigator
- Adequate bone marrow reserve and organ system functions
- Willing to comply with contraceptive restrictions
Критерии исключения
- Any of previous or current treatment prohibited by protocol
- Any unresolved > grade 2 drug-related adverse events
- Lymphoma involving central nervous system
- Any of severe cardiac or pulmonary abnormalities
- Disease condition requires immunosuppressants, biologics, or NSAIDs
- Active infection
- Malignancy disease within five years
- Poorly controlled gastrointestinal disorder or inadequate absorption of medication
- Severe or poorly controlled systemic diseases
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
- Открытое
- Основная цель
- Лечение
Центры проведения
Китай · 36 центров
- Anhui Provincial Cancer Hospital — Хэфэй
- The Second Hospital of Anhui Medical University — Хэфэй
- Beijing Hospital — Пекин
- Beijing Tongren Hospital, CMU — Пекин
- Peking University Third Hospital — Пекин
- The First Affiliated Hospital of Chongqing Medical University — Чунцин
- Fujian Cancer Hospital — Фучжоу
- The First Affiliated Hospital of Xiamen University — Xiamen
- … и ещё 28 центров
Тайвань · 8 центров
- Chang Bing Show Chwan Memorial Hospital — Changhua
- Kaohsiung Chang Gung Memorial Hospital — Kaohsiung City
- Taipei Medical University - Shuang Ho Hospital — New Taipei City
- China Medical University Hospital — Taichung
- Chi Mei Medical Center - Liouying Branch — Tainan
- National Cheng Kung University Hospital — Tainan
- National Taiwan University Hospital — Taipei
- Koo Foundation Sun Yat-Sen Cancer Center — Taipei
Таиланд · 7 центров
- King Chulalongkorn Memorial Hospital — Bangkok
- Mahidol University - Faculty of Medicine - Ramathibodi Hospital — Bangkok
- Phramongkutklao Hospital — Bangkok
- Siriraj Hospital - Mahidol University — Bangkok
- Maharaj Nakorn Chiang Mai Hospital — Chiang Mai
- Prince of Songkla University-Faculty of Medicine — Hat Yai
- Srinagarind Hospital - Faculty of Medicine Khon Kaen University — Khon Kaen
Идентификаторы
NCT: NCT07234162 · DZ2022J0004