- ICH GCP
- Реестр клинических исследований США
- Клиническое испытание NCT02471820
Lenalidomide & Adriamycin & Dexamethasone (RAD) in Newly Diagnosed, Multiple Myeloma Patients (RAD)
14 октября 2016 г. обновлено: Meletios A. Dimopoulos
Phase II Open Label Study for the Assessment of the Efficacy and Safety of Lenalidomide & Adriamycin & Low Dose Dexamethasone (RAD) in Newly Diagnosed, Symptomatic Multiple Myeloma Patients
This study is to assess the efficacy and safety of lenalidomide in combination with adriamycin and low dose dexamethasone in newly diagnosed patients with symptomatic multiple myeloma as well as to collect information regarding the effect of this regimen on angiogenesis and bone remodeling of the study population.
Обзор исследования
Статус
Завершенный
Условия
Вмешательство/лечение
Подробное описание
This is a Phase II, non randomized, non- comparative, open label trial which assess the efficacy and safety of lenalidomide, adriamycin and low dose dexamethasone combination (RAD) in 45 newly diagnosed patients with symptomatic multiple myeloma as well as to collect information regarding the effect of this regimen on angiogenesis and bone remodeling of the study population.
The recruitment period is estimated for 5 months while the treatment period and the follow up period 4 months and 1 month respectively.
During the treatment initiation visit the response to the combination RAD according the International Myeloma Working Group (IMWG) criteria will be evaluated, biochemical markers of bone metabolism and angiogenic cytokines will be measured as well.
IMWG Response evaluation will be repeated the day 1 of each treatment cycle as well as at the response evaluation visit.
Finally biochemical markers of bone metabolism and angiogenic cytokines will be measured once more at the end of treatment visit.
Тип исследования
Интервенционный
Регистрация (Действительный)
45
Фаза
- Фаза 2
Контакты и местонахождение
В этом разделе приведены контактные данные лиц, проводящих исследование, и информация о том, где проводится это исследование.
Места учебы
-
-
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Patra, Греция, 26504
- University General Hospital of Patras
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Thessaloniki, Греция, 54007
- Theageneio Anticancer Hospital of Thessaloniki
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Attica
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Athens, Attica, Греция, 11528
- General Hospital of Athens "Alexandra"
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Athens, Attica, Греция, 11527
- General Hospital of Athens "G. Gennimatas"
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Критерии участия
Исследователи ищут людей, которые соответствуют определенному описанию, называемому критериям приемлемости. Некоторыми примерами этих критериев являются общее состояние здоровья человека или предшествующее лечение.
Критерии приемлемости
Возраст, подходящий для обучения
От 18 лет до 70 лет (Взрослый, Пожилой взрослый)
Принимает здоровых добровольцев
Нет
Полы, имеющие право на обучение
Все
Описание
Inclusion Criteria:
- Subjects able to read and understand the Informed Consent Form (ICF).
- Subjects willing to participate in the study and comply with its procedures.
- Subjects who have signed the ICF
- Newly diagnosed patients with symptomatic MM according to the criteria of IMWG
- Subjects eligible for autologous stem cell transplantation
- Age 18-70 years, of either sex
- karnofsky ≥ 60
- Platelets ≥ 100x109/L
- Neutrophils ≥ 1.5x109/L
- Alanine transaminase (ALT) & Aspartate transaminase (AST) ≤ 3-fold of upper normal limit
- Bilirubin ≤ 2-fold of upper normal limit
- Creatinine clearance ≥60 ml/min
- Expected survival ≥ 6 months as per PI's clinical judgment
- Subjects able to tolerate aspirin, low molecular weight heparin or coumarinic agents as prophylactic anticoagulation
- Female subject of childbearing potential must have 2 negative serum pregnancy tests (hCG) at Screening (once within 10-14 days and once 24 h before the study drug administration) and if sexually active must be using two medically acceptable, highly effective, adequate forms of birth control (ie, failure rate <1% per year when used consistently and correctly) prior to Screening and and for time period at least 28 days before the study drug administration and agree to continue using it while being in the study (Screening and Treatment Periods including dose interruptions). A female subject should continue using a highly effective method of birth control for 30 days following the end of treatment.
- A male subject must agree to use an adequate form of contraception for the duration of the study, while taking the study drug, during dose interruptions at for at least 28 days after the last dose of study drug even if he has had a successful vasectomy and agree to have sexual relations only with women who use a highly effective birth control method.
- Subjects must be free of any clinically significant disease (other than MM) that would interfere with study evaluations
Exclusion Criteria:
- Pregnancy, breastfeeding οr intention of pregnancy during the trial
- Suspected or known hypersensitivity to any of the study drugs
- Ongoing severe infection requiring intravenous antibiotic treatment
- Prior malignancy, except for adequately treated basal cell or squamous cell skin cancer, in-situ cervical cancer, or other cancer from which the subject has been disease-free for at least 5 years. Concurrent prostate cancer for which the patient is receiving therapy will not be considered an exclusion if the Prostatic specific antigen (PSA) has been stable for 3 years
- Solitary bone or solitary extramedullary plasmacytoma as the only evidence of plasma cell dyscrasia
- Myocardial infraction within 6 months before enrollment, New York Heart Association (NYHA) Class II or greater heart failure, uncontrolled angina, severe uncontrolled ventricular arrhythmia, clinically significant pericardial disease, or electrocardiographic evidence of acute ischemic or active conduction system abnormalities
- Uncontrolled medical problems such as diabetes, coronary artery disease, hypertension, unstable angina, arrhythmia, pulmonary, hepatic and renal diseases unless renal insufficiency is considered to be secondary to MM
- Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the ICF
- Any condition, including the presence of laboratory abnormalities, which places the subject at unacceptable risk if he/she will participate in the study or confounds the ability to interpret data from the study
- Subjects with any clinical condition that would affect study's outcome
- Participation in another interventional clinical trial in the 4 weeks preceding enrollment or planning to participate in another interventional clinical trial during the planned period of this study, except of the clinical trials that implicate drugs of supportive treatment
Учебный план
В этом разделе представлена подробная информация о плане исследования, в том числе о том, как планируется исследование и что оно измеряет.
Как устроено исследование?
Детали дизайна
- Основная цель: Уход
- Распределение: Н/Д
- Интервенционная модель: Одногрупповое задание
- Маскировка: Нет (открытая этикетка)
Оружие и интервенции
Группа участников / Армия |
Вмешательство/лечение |
|---|---|
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Экспериментальный: Lenalidomide, adriamycin & dexamethasone
Lenalidomide 25 mg administered orally for the first 21 days of each 28-day-cycle, plus Adriamycin i.v. on days 1,2,3 & 4 of every cycle, plus Dexamethasone 40 mg orally on days 1, 8, 15 & 22 of every cycle for 4 cycles
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Lenalidomide 25 mg by mouth for the first 21 days of a 28-day-cycle for 4 cycles
Другие имена:
Adriamycin as intravenous bolus infusion at a dose of 9 mg/m2, on days 1-4 of a 28-day cycle for 4 cycles
Другие имена:
Dexamethasone by mouth at a dose of 40 mg, on days 1, 8, 15, and 22 of a 28-day cycle for 4 cycles
Другие имена:
|
Что измеряет исследование?
Первичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
Overall response rate
Временное ограничение: 142 days
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Assessment of the overall response rate of study population to RAD regimen (including stringent complete response, complete response, very good partial response, partial response and stable disease) according to the uniform criteria of IMWG (International Myeloma Working Group) regarding the response to multiple myeloma therapy
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142 days
|
Вторичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
Progression-free survival (PFS)
Временное ограничение: 142 days
|
142 days
|
|
|
Time to progression (TTP)
Временное ограничение: 142 days
|
142 days
|
|
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Time to Next Therapy (TtNT)
Временное ограничение: 142 days
|
142 days
|
|
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Number and severity of Adverse events as a measure of safety and toxicity profile
Временное ограничение: 142 days
|
Adverse events will be assessed at each visit and graded according to the National Cancer Institute Common Toxicity Criteria (version 2.0)
|
142 days
|
Другие показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
Number of stem cell collected before Autologous Stem Cell Transplantation (ASCT)
Временное ограничение: 142 days
|
142 days
|
|
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Dickkopf-1 (DKK-1)
Временное ограничение: 1 day
|
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
|
1 day
|
|
Dickkopf-1 (DKK-1)
Временное ограничение: 112 days
|
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
|
112 days
|
|
C-telopeptide of type-I collagen (CTX)
Временное ограничение: 1 day
|
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
|
1 day
|
|
C-telopeptide of type-I collagen (CTX)
Временное ограничение: 112 days
|
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
|
112 days
|
|
Tartrate-resistant acid phosphatase isoform-5b (TRACP-5b)
Временное ограничение: 1 days
|
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
|
1 days
|
|
Tartrate-resistant acid phosphatase isoform-5b (TRACP-5b)
Временное ограничение: 112 days
|
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
|
112 days
|
|
Bone-alkaline phosphatase (bALP)
Временное ограничение: 1 day
|
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
|
1 day
|
|
Bone-alkaline phosphatase (bALP)
Временное ограничение: 112 days
|
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
|
112 days
|
|
Osteocalcin (OC)
Временное ограничение: 1 day
|
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
|
1 day
|
|
Osteocalcin (OC)
Временное ограничение: 112 days
|
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
|
112 days
|
|
C-terminal propeptide of procollagen type-I (CICP)
Временное ограничение: 1 day
|
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
|
1 day
|
|
C-terminal propeptide of procollagen type-I (CICP)
Временное ограничение: 112 days
|
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
|
112 days
|
|
Soluble and total RANKL (sRANKL, tRANKL)
Временное ограничение: 1 day
|
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
|
1 day
|
|
Soluble and total RANKL (sRANKL, tRANKL)
Временное ограничение: 112 days
|
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
|
112 days
|
|
Osteoprotegerin (OPG)
Временное ограничение: 1 day
|
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
|
1 day
|
|
Osteoprotegerin (OPG)
Временное ограничение: 112 days
|
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
|
112 days
|
|
Osteopontin (OPN)
Временное ограничение: 1 day
|
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
|
1 day
|
|
Osteopontin (OPN)
Временное ограничение: 112 days
|
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
|
112 days
|
|
Macrophage inflammatory protein 1-alpha (MIP-1α)
Временное ограничение: 1 day
|
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
|
1 day
|
|
Macrophage inflammatory protein 1-alpha (MIP-1α)
Временное ограничение: 112 days
|
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
|
112 days
|
|
Angiopoietin-1 & -2
Временное ограничение: 1 day
|
Angiogenic cytokines, which will be evaluated in the serum of patients during therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
|
1 day
|
|
Angiopoietin-1 & -2
Временное ограничение: 112 days
|
Angiogenic cytokines, which will be evaluated in the serum of patients during therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
|
112 days
|
|
Angiogenin
Временное ограничение: 1 day
|
Angiogenic cytokines, which will be evaluated in the serum of patients during therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
|
1 day
|
|
Angiogenin
Временное ограничение: 112 days
|
Angiogenic cytokines, which will be evaluated in the serum of patients during therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
|
112 days
|
|
VEGF
Временное ограничение: 1 day
|
Angiogenic cytokines, which will be evaluated in the serum of patients during therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
|
1 day
|
|
Vascular endothelial growth factor (VEGF)
Временное ограничение: 112 days
|
Angiogenic cytokines, which will be evaluated in the serum of patients during therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
|
112 days
|
|
VEGF-A
Временное ограничение: 1 day
|
Angiogenic cytokines, which will be evaluated in the serum of patients during therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
|
1 day
|
|
VEGF-A
Временное ограничение: 112 days
|
Angiogenic cytokines, which will be evaluated in the serum of patients during therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
|
112 days
|
|
basic fibroblast growth factor (bFGF)
Временное ограничение: 1 day
|
Angiogenic cytokines, which will be evaluated in the serum of patients during therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
|
1 day
|
|
basic fibroblast growth factor (bFGF)
Временное ограничение: 112 days
|
Angiogenic cytokines, which will be evaluated in the serum of patients during therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
|
112 days
|
Соавторы и исследователи
Здесь вы найдете людей и организации, участвующие в этом исследовании.
Спонсор
Следователи
- Главный следователь: Meletios Dimopoulos, Doctor, General Hospital of Athens "Alexandra"
- Главный следователь: Eirini Katodritou, Doctor, Theageneio Anticancer Hospital of Thessaloniki
- Главный следователь: Nikolaos Anagnostopoulos, Doctor, General Hospital of Athens "G. Gennimatas''
- Главный следователь: Argirios Symeonidis, Doctor, University General Hospital of Patras
Даты записи исследования
Эти даты отслеживают ход отправки отчетов об исследованиях и сводных результатов на сайт ClinicalTrials.gov. Записи исследований и сообщаемые результаты проверяются Национальной медицинской библиотекой (NLM), чтобы убедиться, что они соответствуют определенным стандартам контроля качества, прежде чем публиковать их на общедоступном веб-сайте.
Изучение основных дат
Начало исследования
1 ноября 2014 г.
Первичное завершение (Действительный)
1 июля 2016 г.
Завершение исследования (Действительный)
1 июля 2016 г.
Даты регистрации исследования
Первый отправленный
5 июня 2015 г.
Впервые представлено, что соответствует критериям контроля качества
10 июня 2015 г.
Первый опубликованный (Оценивать)
15 июня 2015 г.
Обновления учебных записей
Последнее опубликованное обновление (Оценивать)
17 октября 2016 г.
Последнее отправленное обновление, отвечающее критериям контроля качества
14 октября 2016 г.
Последняя проверка
1 октября 2016 г.
Дополнительная информация
Термины, связанные с этим исследованием
Ключевые слова
Дополнительные соответствующие термины MeSH
- Сердечно-сосудистые заболевания
- Сосудистые заболевания
- Заболевания иммунной системы
- Новообразования по гистологическому типу
- Новообразования
- Лимфопролиферативные заболевания
- Иммунопролиферативные заболевания
- Гематологические заболевания
- Геморрагические расстройства
- Нарушения гемостаза
- Парапротеинемии
- Нарушения белков крови
- Множественная миелома
- Новообразования, Плазматические клетки
- Физиологические эффекты лекарств
- Молекулярные механизмы фармакологического действия
- Автономные агенты
- Агенты периферической нервной системы
- Ингибиторы ферментов
- Противовоспалительные агенты
- Противоопухолевые агенты
- Иммунологические факторы
- Противорвотные средства
- Желудочно-кишечные агенты
- Глюкокортикоиды
- Гормоны
- Гормоны, заменители гормонов и антагонисты гормонов
- Противоопухолевые агенты, гормональные
- Ингибиторы протеазы
- Ингибиторы топоизомеразы II
- Ингибиторы топоизомеразы
- Ингибиторы ангиогенеза
- Агенты, модулирующие ангиогенез
- Вещества роста
- Ингибиторы роста
- Антибиотики, Противоопухолевые
- Дексаметазон
- Дексаметазона ацетат
- ББ 1101
- Леналидомид
- Доксорубицин
- Липосомальный доксорубицин
Другие идентификационные номера исследования
- RV-MM-GMSG-392
- 2011-001499-20 (Номер EudraCT)
Планирование данных отдельных участников (IPD)
Планируете делиться данными об отдельных участниках (IPD)?
Не определился
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. .