| Статус: |
Завершено
|
| Протокол № | M20-466 № M20-466 |
| Тип: | ММКИ |
| Фаза: | IIb |
| РКИ № | 523 от 10 сентября 2021 г. |
| Начало: | 10 сентября 2021 г. |
| Окончание: | 31 декабря 2024 г. |
| Пациентов: | 70 |
| Наименование протокола: | Рандомизированное двойное слепое плацебо-контролируемое исследование для оценки безопасности и эффективности ABBV-154 у пациентов с ревматоидным артритом средней и высокой активности с неадекватным ответом на биологические и/или таргетные синтетические модифицирующие болезнь противоревматические препараты (b/tsDMARDs) |
| Цель исследования: | Оценка безопасности и эффективности препарата ABBV-154 по сравнению с плацебо у пациентов с ревматоидным артритом умеренной и высокой активности |
| Препарат(ы): | ABBV-154 |
| Лекарственная форма: | Раствор для подкожного введения, 100 мг/мл (40 мг/0.4 мл, 150 мг/1.5 мл, 80 мг/0.8 мл) |
| Разработчик: | “ЭббВи Инк.” |
| Страна: | США |
| CRO: | ООО "ЭббВи", 000000, г Москва, г 125196, г. Москва, ул. Лесная, д. 7, этаж 4, помещение 1, Россия |
| Терапевтические области: | Иммунология;Ревматология; |
Дополнительная информация:
ClinicalTrials.gov Study to Evaluate Adverse Events and Change in Disease Activity in Participants Between 18 to 75 Years of Age Treated With Subcutaneous (SC) Injections of ABBV-154 for Moderately to Severely Active Rheumatoid Arthritis (RA)
| Статус: | Terminated |
| Фаза: | Phase 2 |
| Начало: | 23 июня 2021 г. |
| Окончание: | 4 августа 2023 г. |
| Описание: | Rheumatoid Arthritis (RA) is an inflammatory disease of the joints causing pain, stiffness, swelling and loss of joint function. This study evaluated how safe and effective ABBV-154 is in participants treated for moderately to severely active RA. Adverse events and change in the disease activity were assessed. ABBV-154 is an investigational drug being evaluated for the treatment of RA. Study doctors placed the participants in 1 of 5 treatment groups or arms; each arm received a different treatment. There was a 1 in 5 chance that participants were assigned to placebo. Participants 18-75 years of age with moderate to severe RA were enrolled. Around 425 participants were to be enrolled in the study at approximately 270 sites worldwide. The study was comprised of a 12 week placebo-controlled period, a double-blind long term extension (LTE) period 1 of 66 weeks, a LTE period 2 of 104 weeks and a follow-up visit 70 days after the last dose of the study drug. In the LTE period 1, participants in the placebo group were re-randomized to receive ABBV-154 at 1 of 2 different doses SC every other week (EOW). Other participants remained on their previous dose and dosing regimen of ABBV-154. There may have been a higher treatment burden for participants in this trial compared to their standard of care. Participants attended regular visits during the study at a hospital or clinic. The effect of the treatment was checked by medical assessments, blood tests, and side effects, and completing questionnaires. |
| смотреть на ClinicalTrials.gov |