- ICH GCP
- Реестр клинических исследований США
- Клиническое испытание NCT01204164
Phase 1 Study of TG02 Citrate in Patients With Advanced Hematological Malignancies (TG02-101)
Phase 1 Dose-Escalation and Pharmacokinetic Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Обзор исследования
Статус
Условия
Вмешательство/лечение
Подробное описание
This is a multicenter, open-label, dose escalation, Phase 1/1b study.
For Parts 1, 2, and 3 of the study, the primary objective is to determine the highest dose of TG02 citrate that can safely be given to patients with different types of hematological malignancy.
For Part 4, the primary objective is to evaluate the safety and tolerability of once-weekly dosing at the maximum-tolerated dose/ Recommended Phase 2 Dose of TG02 in combination with carfilzomib.
This study consists of four parts:
- Part 1: single agent TG02 in acute leukemia patients
- Part 2: single agent TG02 in multiple myeloma patients
- Part 3: TG02 in combination with carfilzomib in multiple myeloma patients
- Part 4: TG02 in combination with carfilzomib in carfilzomib refractory multiple myeloma patients.
Тип исследования
Регистрация (Ожидаемый)
Фаза
- Фаза 1
Контакты и местонахождение
Места учебы
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Colorado
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Denver, Colorado, Соединенные Штаты, 80218
- RMCC
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Georgia
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Atlanta, Georgia, Соединенные Штаты, 30322
- EMORY
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Illinois
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Chicago, Illinois, Соединенные Штаты, 60612
- Rush
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Indiana
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Indianapolis, Indiana, Соединенные Штаты, 46202
- IU
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New Jersey
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Hackensack, New Jersey, Соединенные Штаты, 07601
- HUMC
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New York
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New York City, New York, Соединенные Штаты, 10021
- Cornell
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Ohio
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Columbus, Ohio, Соединенные Штаты, 43210
- OSU
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Tennessee
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Nashville, Tennessee, Соединенные Штаты, 37203
- SCRI
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Texas
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Houston, Texas, Соединенные Штаты, 77030
- MDACC
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-
Критерии участия
Критерии приемлемости
Возраст, подходящий для обучения
Принимает здоровых добровольцев
Полы, имеющие право на обучение
Описание
Part 1 Inclusion Criteria:
- Relapsed AML, ALL, CML in blast crisis, or MDS
- 65+ yrs with AML not eligible for standard frontline chemo
- Interval from prior treatment to time of study drug at least 5 half-lives for cytotoxic/ noncytotoxic agents.
- Persistent clinically significant toxicities from prior chemo ≤ Grd 1
- ECOG PS 0-2
Lab values:
- Cr ≤ 2X ULN
- ALT and/or AST ≤2.5 X ULN
- Total bilirubin ≤1.5 X ULN unless considered due to Gilbert's syndrome
- Negative pregnancy test
- Can take oral med
Part 2 Inclusion Criteria:
- Relapsed multiple myeloma. At least ≥1 line of therapy and progressed after ≥1 prior therapy
Measurable disease defined as at least one of the following:
- Serum M ≥500 mg/dL
- Urine M ≥200 mg per 24hr
- Involved FLC ≥10 mg/dL and abnormal FLC ratio in serum (<0.26 or >1.65)
- Measurable soft tissue plasmacytoma
- Persistent clinically significant toxicities from prior chemo ≤ Grd 1
- ECOG PS 0-2
Lab values:
- ANC of >1000/mm3
- Platelets ≥50,000/mm3
- Cr ≤2X the ULN
- ALT and/or AST ≤2.5X ULN
- Total bilirubin ≤1.5X ULN, unless considered due to Gilbert's syndrome
- Negative pregnancy test
- Can take oral med
Part 3 Inclusion Criteria:
Measurable disease defined as at least one of the following:
- Serum M ≥500 mg/dL
- Urine M protein ≥200 mg per 24hr
- Involved FLC level ≥10 mg/dL and abnormal FLC ratio in serum (<0.26 or >1.65)
Meet at least one of the criteria below:
- a. ≥2 prior therapies including proteasome inhibitor and immunomodulatory agent (IMiD)
- b. ≥1 prior therapy and one of the following abnormalities: 17p del, p53, 1q amp, 1p del, t(4;14)
- Interval from prior treatment to time of study drug at least 5 half-lives or 3 wks, which ever is shorter, for noncytotoxic agents
- Persistent clinically significant toxicities from prior chemo ≤ Grd 1 or Grd 2 neuropathy without pain
- ECOG PS 0-2
Lab values:
- ANC of >1000/mm3 independent of G-CSF
- Platelets ≥50,000/mm3 independent of transfusion
- MDRD calculated or measured CrCl of ≥30 mL/min
- ALT and/or AST ≤3X ULN
- Total bilirubin ≤2X ULN, unless considered due to Gilbert's syndrome
- Negative pregnancy test
- Can take oral med
Part 4 Inclusion Criteria:
Measurable disease defined as at least one of the following:
- Serum M ≥500 mg/dL
- Urine M protein ≥200 mg per 24hr
- Involved FLC level ≥10 mg/dL and an abnormal FLC ratio in serum (<0.26 or >1.65)
Received prior therapies including:
- a. bortezomib
- b. an IMiD
- c. carfilzomib. Demonstrated disease progression on or within 60d of completion of carfilzomib therapy
- Interval from prior treatment to time of study drug at least 5 half-lives or 3 wks, which ever is shorter, for noncytotoxic agents.
- Persistent clinically significant toxicities from prior chemo ≤ Grd 1, or Grd 2 neuropathy without pain.
- ECOG PS 0-2
Lab values:
- ANC of >1000/mm3 independent of G-CSF
- Platelets ≥50,000/mm3 independent of transfusion
- MDRD calculated or measured CrCl of ≥30 mL/min
- ALT and/or AST ≤3X ULN
- Total bilirubin ≤2X ULN, unless considered due to Gilbert's syndrome
- Negative pregnancy test
- Can take oral med
Parts 1 and 2 Exclusion Criteria:
- Previous allogenic hematopoietic transplant within 90 d
- Concurrent severe or uncontrolled medical disease that would compromise the safety or compromise the ability of the patient to complete the study
- Prolonged QTC interval >450ms
- Symptomatic CNS metastases
- Known HIV or AIDS
- Actively treated for a second malignancy
- Pregnant or nursing women
Part 3 Exclusion Criteria:
- Multiple myeloma of IgM subtype, POEMS, plasma cell leukemia
- Corticosteroids discontinued ≥7 days of initiating therapy
- Previous chemo within 2 wks
- Hx of ventricular arrhythmia or symptomatic conduction abnormality within 12m
- CHF, symptomatic ischemia, conduction abnormalities uncontrolled by conventional intervention, myocardial infarction within 6m
- Prolonged QTc interval (males >450ms, females >470ms)
- Previous allogeneic hematopoietic transplant within 90 days of study enrollment, Active GVHD requiring treatment.
- Concurrent severe or uncontrolled medical disease that would compromise the safety or compromise the ability of the patient to complete the study
- Symptomatic CNS metastases
- Known HIV or AIDS
- Prior or 2nd malignancy, except non-melanoma skin cancer, completely resected cervical or prostate cancer (with PSA of less than or equal to 0.1 ng/ml), or other cancer for which the subject has received curative therapy at least 3 yrs prior to study entry
- Treatment-related MDS
- Significant neuropathy (Grd 3-4 or Grd 2 with pain) at the time of 1st dose
- Primary AL amyloidosis
- Pleural effusions requiring thoracentesis or ascites requiring paracentesis
- Pregnant or nursing women
Part 4 Exclusion Criteria:
- Multiple myeloma of IgM subtype, POEMS, plasma cell leukemia
- Previous chemo within 2 wks
- Hx ventricular arrhythmia or symptomatic conduction abnormality within 12m
- CHF, symptomatic ischemia, conduction abnormalities uncontrolled by conventional intervention, and myocardial infarction within 6m
- Prolonged QTc interval (males >450ms, females >470ms)
- Previous allogeneic hematopoietic transplant within 90 days. Active GVHD requiring treatment
- Concurrent severe or uncontrolled medical disease that would compromise the safety or compromise the ability of the patient to complete study
- Symptomatic CNS metastases
- Known HIV or AIDS
- Prior or 2nd malignancy, except non-melanoma skin cancer, completely resected cervical or prostate cancer (with PSA of less than or equal to 0.1 ng/ml), or other cancer for which the subject has received curative therapy at least 3 yrs prior to study entry
- Treatment-related MDS
- Significant neuropathy (Grd 3-4 or Grd 2 with pain) at the time of 1st dose
- Primary AL amyloidosis
- Pleural effusions requiring thoracentesis or ascites requiring paracentesis
- Pregnant or nursing women
Учебный план
Как устроено исследование?
Детали дизайна
- Основная цель: Уход
- Распределение: Нерандомизированный
- Интервенционная модель: Одногрупповое задание
- Маскировка: Нет (открытая этикетка)
Оружие и интервенции
Группа участников / Армия |
Вмешательство/лечение |
|---|---|
|
Экспериментальный: TG02 in AL
Single agent TG02 citrate in acute leukemia patients
|
TG02 citrate capsules given orally.
Другие имена:
|
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Экспериментальный: TG02 in MM
Single Agent TG02 citrate in multiple myeloma patients
|
TG02 citrate capsules given orally.
Другие имена:
|
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Экспериментальный: TG02 + CFZ in MM
TG02 in combination with carfilzomib and dexamethasone in multiple myeloma patients
|
TG02 citrate capsules given orally.
Другие имена:
Carfilzomib per PI
Другие имена:
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Экспериментальный: TG02 + CFZ + DEX in CFZ refractory MM
TG02 in combination with carfilzomib and dexamethasone in carfilzomib refractory multiple myeloma patients
|
TG02 citrate capsules given orally.
Другие имена:
Carfilzomib per PI
Другие имена:
Dexamethasone (Oral or IV)
Другие имена:
|
Что измеряет исследование?
Первичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
Maximum Tolerated Dose
Временное ограничение: 28 days
|
Maximum Tolerated Dose refers to the highest dose of TG02 administered that will produce the desired effect without unacceptable toxicity.
|
28 days
|
Вторичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
Safety
Временное ограничение: 28 days
|
Safety data will include vital signs, ECGs, PE findings, clinical laboratory parameters, ECOG PS, AEs/SAEs and concomitant medications.
|
28 days
|
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Pharmacokinetics of TG02
Временное ограничение: 28 days
|
Plasma will be analyzed to determine TG02 concentration.
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28 days
|
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Clinical Benefit Response
Временное ограничение: 28 days
|
Clinical Benefit Response is defined as the sum of all response categories for Overall Response Rate (ORR is defined as the sum of patients with sCR, CR, VGPR and PR) plus minimal response (MR).
|
28 days
|
|
Overall Response Rate
Временное ограничение: 28 days
|
Overall Response Rate is defined as the sum of patients with sCR, CR, VGPR and PR.
|
28 days
|
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Progression-Free Survival
Временное ограничение: 28 days
|
Progression-Free Survival is the time to disease progression or death, which is measured from the date of first study drug administration until the first date that recurrent or progressive disease is objectively documented or the date of death.
|
28 days
|
|
Overall Survival
Временное ограничение: 28 days
|
Overall Survival is time to death, which is measured from the date of first study drug administration until the date of death.
|
28 days
|
|
Duration of Response
Временное ограничение: 28 days
|
Duration of Response is the duration from first observation of response to the first documentation of disease progression, with deaths from causes other than disease progression censored.
For the purposes of the calculation of the DOR, the date at which the response status was first observed rather than the date of confirmation is used as the start date.
|
28 days
|
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Pharmacodynamics
Временное ограничение: 28 days
|
Pharmacodynamic sampling may include whole blood and bone marrow at baseline and post-treatment for pathway determination if available.
|
28 days
|
Соавторы и исследователи
Спонсор
Следователи
- Директор по исследованиям: T Parrott, Tragara Pharmaceuticals
Даты записи исследования
Изучение основных дат
Начало исследования
Первичное завершение (Действительный)
Завершение исследования (Действительный)
Даты регистрации исследования
Первый отправленный
Впервые представлено, что соответствует критериям контроля качества
Первый опубликованный (Оценивать)
Обновления учебных записей
Последнее опубликованное обновление (Оценивать)
Последнее отправленное обновление, отвечающее критериям контроля качества
Последняя проверка
Дополнительная информация
Термины, связанные с этим исследованием
Ключевые слова
Дополнительные соответствующие термины MeSH
- Патологические процессы
- Сердечно-сосудистые заболевания
- Сосудистые заболевания
- Заболевания иммунной системы
- Новообразования по гистологическому типу
- Новообразования
- Лимфопролиферативные заболевания
- Иммунопролиферативные заболевания
- Новообразования по локализации
- Заболевания костного мозга
- Гематологические заболевания
- Геморрагические расстройства
- Миелопролиферативные заболевания
- Нарушения гемостаза
- Парапротеинемии
- Нарушения белков крови
- Неопластические процессы
- Новообразования, Плазматические клетки
- Лейкемия
- Трансформация клеток, новообразования
- Канцерогенез
- Лейкоз, миелоидный
- Лейкоз, миелогенный, хронический, BCR-ABL положительный
- Гематологические новообразования
- Множественная миелома
- Взрывной кризис
- Физиологические эффекты лекарств
- Автономные агенты
- Агенты периферической нервной системы
- Противовоспалительные агенты
- Противоопухолевые агенты
- Противорвотные средства
- Желудочно-кишечные агенты
- Глюкокортикоиды
- Гормоны
- Гормоны, заменители гормонов и антагонисты гормонов
- Противоопухолевые агенты, гормональные
- Дексаметазон
Другие идентификационные номера исследования
- TG02-101
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. .