| Статус: |
Завершено
|
| Протокол № | 16349 № 16349 |
| Тип: | ММКИ |
| Фаза: | IIb |
| РКИ № | 690 от 1 ноября 2013 г. |
| Начало: | 1 января 2014 г. |
| Окончание: | 30 июня 2023 г. |
| Пациентов: | 16 |
| Наименование протокола: | Открытое неконтролируемое исследование II фазы ингибитора PI3K BAY 80-6946, вводимого внутривенно, у пациентов с рецидивом индолентной или агрессивной неходжкинской лимфомы |
| Цель исследования: | Целью исследования (часть B) является оценка эффективности и безопасности BAY 80 6946 у пациентов с рецидивом фолликулярной лимфомы после устойчивости к стандартному лечению. Дополнительные цели – оценка фармакокинетики BAY 80 6946, биомаркеров и качества жизни. |
| Препарат(ы): | BAY 80-6946 |
| Лекарственная форма: | Лиофилизат для приготовления раствора для внутривенного введения 80 мг/4 мл (флаконы). |
| Разработчик: | Байер АГ |
| Страна: | Германия |
| CRO: | ЗАО "Байер", 123022 г. Москва, Большой Трехгорный пер., дом 1, строение 1, Россия |
| Терапевтические области: | Гематология;Онкология; |
Дополнительная информация:
ClinicalTrials.gov Open-label, Uncontrolled Phase II Trial of Intravenous PI3K Inhibitor BAY80-6946 in Patients With Relapsed, Indolent or Aggressive Non-Hodgkin's Lymphomas
| Статус: | Completed |
| Фаза: | Phase 2 |
| Начало: | 19 ноября 2012 г. |
| Окончание: | 18 мая 2023 г. |
| Описание: | The objective of the study (part A) is to evaluate the efficacy and safety of BAY80-6946 in patients with indolent or aggressive Non-Hodgkin's Lymphoma, who have progressed after standard therapy. 30 patients will be enrolled to both indolent and aggressive disease group. The objective of the study part B (CHRONOS-1) is to evaluate the efficacy and safety of BAY80-6946 in patients with relapsed/refractory follicular lymphoma. 120 patients will be enrolled in the part B of the study. Further objectives are to evaluate the pharmacokinetics and biomarkers. Quality of life will be a further objective of part B of the study. In a cohort of 20 patients (enrolled both in part A and B) an ECG substudy will be performed to assess the potential for cardiac toxicity and QT/QTc interval prolongation of BAY80-6946. After an up to 28-day screening period, eligible patients will start treatment with BAY80-6946 at a dose of 0.8 mg/kg (Part A) and at a dose of 60 mg (Part B). Treatment will be continued until disease has progressed or until another criterion is met for withdrawal from study. An end-of-treatment visit will be performed within 7 days after discontinuation of study treatment. Thirty to 35 days after last study drug administration, a safety followup visit will be performed for the collection of adverse events (AEs) and concomitant medication data. Patients will be contacted quarterly to determine overall survival status up to 4 years after last patient completed treatment. Patients who discontinue study drug for reasons other than disease progression will enter the Active Assessment Follow-up period. The end of study notification to Health Authorities will be based on the completion of the collection of survival data. The efficacy is measured by the decrease in tumor size. Tumor assessments will be done at Screening, every 8 weeks during Year 1, every 12 weeks during Year 2, and every 6 months during Year 3. Blood samples will be collected for pharmacokinetic analysis. Archival tumor tissue and blood samples will be collected for biomarker analysis (mandatory) and for central pathology review (part B), fresh biopsy tissue will also be collected if available. |
| смотреть на ClinicalTrials.gov |