A Study of Mirikizumab (LY3074828) in Pediatric Participants With Crohn's Disease
Ориентир для пациента и семьи
Простыми словами
Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.
- Что изучают
- В протоколе указаны: Mirikizumab.
- Кому может быть актуально
- Состояния в реестре: Crohn's Disease. Базовые параметры: 2 лет — 17 лет · Все.
- Что важно проверить
- Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
- Где проводится
- США, Австрия, Бельгия, Бразилия, Канада +11
- Следующий шаг
- Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
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Официальное название
A Phase 3, Multicenter, Randomized Clinical Study to Evaluate Mirikizumab in Pediatric Crohn's Disease
Обзор
Study participants will be screened during the platform study and randomly assigned to receive mirikizumab or another intervention. The purpose of the mirikizumab study is to evaluate efficacy, safety, tolerability, and how well mirikizumab absorbs into the body of pediatric participants with Crohn's disease. Study periods for the intervention-specific appendix (ISA) will be as follows: * A 12-week induction period * A maintenance period from Week 12 to Week 52, and * A safety follow-up period up to 16 weeks. The study will last about 74 weeks and may include up to 19 visits.
Подробное описание
Participants screened in the MACARONI-23 Platform study could be randomized to mirikizumab to participate in this intervention specific arm of the study.
Вмешательства
- Препарат Mirikizumab
Administered IV or SC
Первичные конечные точки
- Percentage of Participants with Clinical Response by Pediatric Crohn's Disease Activity Index (PCDAI) at Week 12 and Endoscopic Response by Simple Endoscopic Score for CD (SES-CD) at Week 52 [Срок оценки: Baseline to Week 52]
- Percentage of Participants with a Clinical Response by PCDAI at Week 12 and Clinical Remission by PCDAI at Week 52 [Срок оценки: Baseline to Week 52]
Вторичные конечные точки (12)
- Percentage of Participants Achieving Clinical Response by PCDAI [Срок оценки: Week 12]
- Percentage of Participants Achieving Clinical Response by Clinical Disease Activity Index (CDAI) [Срок оценки: Week 12]
- Percentage of Participants Achieving Clinical Remission by PCDAI [Срок оценки: Week 12]
- Percentage of Participants Achieving Clinical Remission by CDAI [Срок оценки: Week 12]
- Percentage of Participants Who Achieve PCDAI Clinical Response at Week 12 and PCDAI Clinical Remission and Endoscopic Remission at Week 52 [Срок оценки: Baseline to Week 52]
- Percentage of Participants Who Achieve PCDAI Clinical Remission and Endoscopic Remission at Week 52 [Срок оценки: Week 52]
- Percentage of Participants Achieving Clinical Response by PCDAI at Week 12 and Endoscopic Remission by SES-CD at Week 52 [Срок оценки: Baseline to Week 52]
- Change from Baseline in C-reactive Protein (CRP) [Срок оценки: Baseline, Week 12]
- Change from Baseline in CRP [Срок оценки: Baseline, Week 52]
- Change from Baseline in Fecal calprotectin [Срок оценки: Baseline, Week 12]
- Change from Baseline in Fecal calprotectin [Срок оценки: Baseline, Week 52]
- Percentage of Participants Achieving Clinical Response PCDAI at Week 12 and Clinical Remission by CDAI at Week 52 [Срок оценки: Baseline to Week 52]
Критерии участия
Критерии включения
- Participants must have a diagnosis of CD or fistulizing CD, with active colitis, ileitis, or ileocolitis, confirmed at any time in the past by clinical, endoscopic, and histologic criteria.
- Participants have moderately to severely active CD (as defined by a baseline PCDAI score ≥30).
- Participants must have endoscopy with evidence of active CD defined as SES-CD score ≥6 (or ≥4 for participants with isolated ileal disease) within 1 month of receiving study intervention at Week 0.
- Participants must have a documented history of inadequate response, loss of response or intolerance to at least one medication used to treat CD, which may include immunomodulators, oral or IV corticosteroids, a biologic therapy or a JAK inhibitor.
Критерии исключения
- Participants must not have complications of CD such as symptomatic strictures or stenosis, short gut syndrome, or any other manifestations that might be anticipated to require surgery.
- Participants must not have an abscess.
- Participants must not have any kind of bowel resection within 26 weeks or any other intra-abdominal surgery within 12 weeks of baseline.
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Нет
Дизайн исследования
- Распределение
- Нерандомизированное
- Модель
- Параллельные группы
- Маскирование
- Открытое
- Основная цель
- Лечение
Центры проведения
США · 15 центров
- Cedars Sinai Medical Center — Los Angeles
- Connecticut Children's Medical Center — Hartford
- Emory University — Atlanta
- Children's Center for Digestive Health Care, LLC — Atlanta
- Riley Childrens Hospital — Indianapolis
- Boston Children's Hospital — Boston
- Atlantic Children's Health--Pediatric Gastroenterology — Morristown
- Weill Cornell Medical College (WCMC) - Judith Jaffe Multiple Sclerosis Center (JJMSC) — New York
- … и ещё 7 центров
Япония · 12 центров
- Juntendo University Hospital — Bunkyō City
- Hirosaki University Hospital — Hirosaki
- Kagoshima University Hospital — Kagoshima
- Kokikai Tsujinaka Hospital Kashiwanoha — Kashiwa-shi
- Kobe University Hospital — Kobe
- Saga University Hospital — Saga
- Miyagi Children's Hospital — Sendai
- National Center for Child Health and Development — Setagaya-ku
- … и ещё 4 центра
Бразилия · 7 центров
- Hospital PUC-CAMPINAS — Campinas
- Hospital Pequeno Príncipe — Curitiba-PR
- Hospital das Clínicas - UFG (Universidade Federal de Goiás) — Goiânia
- Hospital de Clínicas de Porto Alegre — Porto Alegre
- Irmandade da Santa Casa de Misericórdia de Porto Alegre — Porto Alegre
- NDI - Nucleo de Doenças Infecciosas — Santos Dumont
- Integral Pesquisa e Ensino — Votuporanga
Израиль · 6 центров
- Soroka Medical Center — Beersheba
- Shamir Medical Center (Assaf Harofeh) — Israel
- Shaare Zedek — Jerusalem
- Hadassah University Hospital, Ein Kerem, — Jerusalem
- Schneider Children's Medical Center — Petah Tikva
- Kaplan Medical Center, Pediatric Gastroenterology Dept. — Rehovot
Италия · 6 центров
- Azienda Ospedaliero-Universitaria SS. Antonio e Biagio e C. Arrigo — Alessandria
- Asst Papa Giovanni Xxiii Bergamo — Bergamo
- Azienda USL di Bologna — Bologna
- SOC Gastroenterologia e Nutrizione - AOU Meyer (Primo Piano Ala OVEST, accettazione DH cen — Florence
- Ospedale dei Bambini Vittore Buzzi — Milan
- Gastroenterologia ed epatologia pediatrica (Piano terra della Clinica Pediatrica) — Roma
Великобритания · 6 центров
- Royal Hospital for Children and Young People — Edinburgh
- Oxford University Hospitals NHS trust John Radcliffe hospital — Headington
- Great Ormond Street Hospital For Children NHS Foundation Trust — London
- Manchester University NHS Foundation Trust — Manchester
- Sheffield Children's Hospital — Sheffield
- … и ещё 1 центр
South Korea · 5 центров
- Inje University Haeundae Paik Hospital — Busan
- Kyungpook National University Chilgok Hospital — Daegu
- Severance Hospital, Yonsei University Health System — Seoul
- Samsung Medical Center — Seoul
- Seoul National University Hospital — Seoul
Бельгия · 4 центра
- Universitair Ziekenhuis Brussel — Brussels
- Cliniques universitaires Saint-Luc — Brussels
- Universitair Ziekenhuis Gent — Ghent
- UZ Leuven — Leuven
Канада · 4 центра
- IWK Health Centre — Halifax
- London Health Sciences Centre (LHSC) - Victoria Hospital — London
- The Hospital for Sick Children — Toronto
- Children's & Women's Health Centre of British Columbia — Vancouver
Норвегия · 4 центра
- Akershus Universitetssykehus — Nordbyagen
- Oslo University Hospital — Oslo
- Universitetssykehuset Nord-Norge — Tromsø
- St-Olavs Hospital — Trondheim
Польша · 3 центра
- Korczowski Bartosz, Gabinet Lekarski — Rzeszów
- Warsaw IBD Point Profesor Kierkus — Warsaw
- Instytut Pomnik-Centrum Zdrowia Dziecka — Warsaw
Португалия · 3 центра
- Centro Clínico Académico - Braga (2CA-Braga) (Hospital de Braga) — Braga
- Centro Hospitalar de Lisboa Norte, E.P.E. - Hospital de Santa Maria — Lisbon
- Centro Hospitalar de São João, E.P.E. — Porto
Испания · 3 центра
- Hospital Universitario Reina Sofia — Córdoba
- Corporacio Sanitaria Parc Tauli — Sabadell
- Hospital Universitari i Politecnic La Fe — Valencia
Австрия · 1 центр
- AKH - Medizinische Universtität Wien — Vienna
Франция · 1 центр
- URC CIC — Paris
Нидерланды · 1 центр
- Erasmus Medisch Centrum — Rotterdam
Идентификаторы
NCT: NCT05509777 · 16632 · I6T-MC-AMAY · MACARONI-23 · PLATFORMPBCRD3001 · I6T-MC-PIBD · 2024-511472-32-00