| Статус: | Проводится | 
                                | Протокол № | EFC16819 EFC16819 № EFC16819 | 
                                | Тип: | ММКИ | 
                                | Фаза: | III | 
                                | РКИ № | 49 от 29 января 2021 г. | 
                                | Начало: | 29 января 2021 г. | 
                                | Окончание: | 30 декабря 2024 г. | 
                                | Пациентов: | 60 | 
                                | Наименование протокола: | Рандомизированное, двойное слепое, плацебо-контролируемое исследование III фазы в параллельных группах для оценки эффективности, безопасности и переносимости SAR440340/REGN3500/итепекимаба (мАТ к ИЛ-33) у пациентов с хронической обструктивной болезнью легких (ХОБЛ) от умеренной до тяжелой степени | 
                                | Цель исследования: | Оценка эффективности, безопасности и переносимости итепекимаба у пациентов с хронической обструктивной болезнью легких (ХОБЛ) от умеренной до тяжелой степени. | 
                                | Препарат(ы): | Итепекимаб (SAR440340/REGN3500) | 
                                | Лекарственная форма: | Раствор для подкожного введения, 150 мг/мл | 
                                | Разработчик: | Санофи-авентис Ресерч энд Девелопмент | 
                                | Страна: | Франция | 
                                | CRO: | Представительство АО "Санофи-авентис груп" (Франция), г.Москва, Российская Федерация, 125009, г. Москва, ул. Тверская, 22, ~ | 
                                | Терапевтические области: | Пульмонология; | 
                            
                            
                            
                            
                                
                                     Дополнительная информация:
                                
                             
                              ClinicalTrials.gov Study to Assess the Efficacy, Safety, and Tolerability of SAR440340/REGN3500/Itepekimab in Chronic Obstructive Pulmonary Disease (COPD) 
                            
                                | Статус: | Active, not recruiting | 
                                | Фаза: | Phase 3 | 
                                | Начало: | 12 февраля 2021 г. | 
                                | Окончание: | 8 сентября 2025 г. | 
                                | Описание: | Primary Objective: Primary population (former smokers cohort): - Evaluate the efficacy of itepekimab compared with placebo on the annualized rate of acute moderate-or-severe COPD exacerbations in former smokers with moderate-to-severe COPD Secondary Objectives: Primary population (former smokers cohort): - Evaluate the efficacy of itepekimab compared with placebo on pulmonary function in former smokers with moderate-to-severe COPD - Evaluate the efficacy of itepekimab compared with placebo on occurrence of acute exacerbation of COPD (AECOPD) in former smokers with moderate-to-severe COPD - Evaluate the efficacy of itepekimab compared with placebo on severe AECOPD in former smokers with moderate-to-severe COPD - Evaluate the efficacy of itepekimab compared with placebo on corticosteroid-treated AECOPD in former smokers with moderate-to-severe COPD - Evaluate the efficacy of itepekimab compared with placebo on respiratory symptoms in former smokers with moderate-to-severe COPD - Evaluate the efficacy of itepekimab compared with placebo on Forced Expiratory Volume in 1 second (FEV1) slope in former smokers with moderate-to-severe COPD - Evaluate the efficacy of itepekimab compared with placebo on health-related quality of life (HRQoL) as assessed by St. George's Respiratory Questionnaire (SGRQ) in former smokers with moderate-to-severe COPD - Evaluate the safety and tolerability of itepekimab in former smokers with moderate-to-severe COPD - Evaluate the pharmacokinetic (PK) profile of itepekimab in former smokers with moderate-to-severe COPD - Evaluate immunogenicity to itepekimab in former smokers with moderate-to-severe COPD Secondary population (current smokers cohort) - Estimate the efficacy of itepekimab compared with placebo on the annualized rate of acute moderate or severe COPD exacerbations in current smokers with moderate-to-severe COPD - Estimate the efficacy of itepekimab compared with placebo on pulmonary function in current smokers with moderate-to-severe COPD - Estimate the safety and tolerability of itepekimab in current smokers with moderate-to-severe COPD - Estimate the PK profile of itepekimab in current smokers with moderate to severe COPD - Estimate immunogenicity to itepekimab in current smokers with moderate-to-severe COPD | 
                                |  | смотреть на ClinicalTrials.gov |