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Идёт набор NCT04844606

A Master Protocol (AMAZ): A Study of Mirikizumab (LY3074828) in Pediatric Participants With Ulcerative Colitis or Crohn's Disease (SHINE-ON)

Фаза III С лечением Ulcerative Colitis Ulcerative Colitis Chronic Inflammatory Bowel Diseases 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, Mirikizumab.
Кому может быть актуально
Состояния в реестре: Ulcerative Colitis, Ulcerative Colitis Chronic, Inflammatory Bowel Diseases, Crohn's Disease. Базовые параметры: 2 лет — 19 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 →
Официальное название

A Master Protocol for a Phase 3, Multicenter, Open-label, Long-term Extension Study to Evaluate the Long-term Efficacy and Safety of Mirikizumab in Children and Adolescents With Moderate-to-severe Ulcerative Colitis or Crohn's Disease

Обзор

The main purpose of this study is to evaluate the long-term efficacy of mirikizumab in pediatric participants with ulcerative colitis (UC) or Crohn's disease (CD). The study will last about 172 weeks and may include up to 44 visits. Additional treatment may be available to participants via a Continued Access Period.

Вмешательства

  • Препарат Mirikizumab
    Administered SC
  • Препарат Mirikizumab
    Administered IV

Первичные конечные точки

  • Percentage of Participants with UC in Modified Mayo Score (MMS) Clinical Remission [Срок оценки: Week 52]
  • Percentage of Participants with CD in Pediatric Crohn's Disease Activity Index (PCDAI) Clinical Remission [Срок оценки: Week 52]
Вторичные конечные точки (12)
  • Percentage of Participants with UC in MMS Clinical Response [Срок оценки: Week 52]
  • Percentage of Participants with CD in PCDAI Clinical Response [Срок оценки: Week 52]
  • Percentage of Participants with UC in Pediatric Ulcerative Colitis Activity Index (PUCAI) Clinical Response [Срок оценки: Week 52]
  • Percentage of Participants with UC in PUCAI Clinical Remission [Срок оценки: Week 52]
  • Percentage of Participants with UC in Endoscopic Remission [Срок оценки: Week 52]
  • Percentage of Participants with CD in Endoscopic Remission [Срок оценки: Week 52]
  • Percentage of Participants with UC in Endoscopic Response [Срок оценки: Week 52]
  • Percentage of Participants with CD in Endoscopic Response [Срок оценки: Week 52]
  • Percentage of Participants with UC in having Endoscopic Subscore = 0 [Срок оценки: Week 52]
  • Percentage of Participants with UC Histologic-Endoscopic Mucosal Remission [Срок оценки: Week 52]
  • Percentage of Participants with CD Achieving Histologic Remission [Срок оценки: Week 52]
  • Percentage of Participants with UC in Corticosteroid-free Remission Without Surgery [Срок оценки: Week 52]

Критерии участия

Критерии включения

  • Participants from originating studies (I6T-MC-AMBA \[NCT05784246\], I6T-MC-AMBU \[NCT04004611\], I6T-MC-AMAM \[NCT03926130\]) , I6T-MC-AMAY \[NCT05509777\]) who would, in the opinion of the investigator, derive clinical benefit from further treatment with mirikizumab
  • Participants from prior studies who have completed assessments and procedures at last visit of originating study and remain on study drug treatment.
  • Female participants must agree to contraception requirements.

Критерии исключения

  • Participants must not have developed a serious adverse event (SAE) or Adverse Event (AE) in originating study or developed other condition before first visit of Study AMAZ that continued treatment with mirikizumab would present an unreasonable risk for the participant.
  • Participants must not have had permanently or temporarily stopped study drug in the originating study, such that restarting mirikizumab would pose an unacceptable risk for the participant in Study AMAZ.
  • Participants must not have an unstable or uncontrolled illness that would potentially affect participant safety.
  • Participants must not be enrolled in the study if, for any reason, being in the study would compromise the participant's safety or confound data interpretation.
  • Participants must not have adenomatous polyps that have not been removed.
  • Participants must not be pregnant or breastfeeding.

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 · 11 центров
  • UCSF Medical Center at Mission Bay — San Francisco
  • Connecticut Children's Medical Center — Hartford
  • Emory University School of Medicine — Atlanta
  • Children's Center for Digestive Health Care, LLC — Atlanta
  • Boston Children's Hospital — Boston
  • Massachusetts General Hospital — Waltham
  • Washington University School of Medicine — St Louis
  • Icahn School of Medicine at Mount Sinai — New York
  • … и ещё 3 центра
Бразилия · 7 центров
  • Centro de Pesquisa Sao Lucas — Campinas
  • Hospital Pequeno Príncipe / Associação Hospitalar de Proteção à Infância — Curitiba
  • Universidade Federal de Goias — Goiânia
  • Hospital de Clinicas de Porto Alegre — Porto Alegre
  • Irmandade da Santa Casa de Misericórdia de Porto Alegre — Porto Alegre
  • Hospital Universitario Cassiano Antonio de Moraes — Vitória
  • Integral Pesquisa e Ensino — Votuporanga
Израиль · 6 центров
  • Soroka Medical Center — Beersheba
  • Rambam Health Care Campus — Haifa
  • Shaare Zedek Medical Center — Jerusalem
  • Hadassah Medical Center — Jerusalem
  • Schneider Children's Medical Center — Petah Tikva
  • Yitzhak Shamir Medical Center — Ẕerifin
Италия · 6 центров
  • Azienda Socio Sanitaria Territoriale Papa Giovanni XXIII — Bergamo
  • Ospedale Maggiore Azienda USL di Bologna — Bologna
  • Azienda Ospedaliera Universitaria Meyer IRCCS — Florence
  • Ospedale dei Bambini Vittore Buzzi — Milan
  • AOU Policlinico Umberto I — Roma
  • Ospedale Pediatrico Bambino Gesù IRCCS — Rome
Япония · 6 центров
  • Institute of Science Tokyo Hospital — Bunkyō
  • Juntendo University Hospital — Bunkyō City
  • Tsujinaka Hospital - Kashiwanoha — Kashiwa
  • Kobe University Hospital — Kobe
  • National Center for Child Health and Development — Tokyo
  • Yokohama City University Medical Center — Yokohama
Бельгия · 5 центров
  • UZ Brussel — Brussels
  • Cliniques universitaires Saint-Luc — Brussels
  • Antwerp University Hospital — Edegem
  • UZ Gent — Ghent
  • UZ Leuven — Leuven
Польша · 5 центров
  • Korczowski Bartosz, Gabinet Lekarski — Rzeszów
  • Twoja Przychodnia SCM — Szczecin
  • Medical Network Spółka z o.o. WIP Warsaw IBD Point Profesor Kierkuś — Warsaw
  • Centrum Zdrowia Dziecka w Warszawie — Warsaw
  • Centrum Medyczne Oporów — Wroclaw
Норвегия · 4 центра
  • Akershus Universitetssykehus — Lørenskog
  • Oslo Universitetssykehus Ullevål — Oslo
  • Universitetssykehuset Nord-Norge HF — Tromsø
  • St. Olavs Hospital — Trondheim
Испания · 4 центра
  • Hospital Universitario Reina Sofia — Córdoba
  • Hospital Sant Joan de Déu — Esplugues de Llobregat
  • Hospital Universitari Parc Tauli — Sabadell
  • Hospital Universitari i Politecnic La Fe — Valencia
South Korea · 3 центра
  • Kyungpook National University Chilgok Hospital — Deagu
  • Seoul National University Hospital — Seoul
  • Samsung Medical Center — Seoul
Великобритания · 3 центра
  • Royal London Hospital — London
  • The John Radcliffe Hospital — Oxford
  • Sheffield Children's Hospital — Sheffield
Канада · 2 центра
  • London Health Sciences Centre — London
  • The Hospital for Sick Children — Toronto
Германия · 2 центра
  • Universitätsmedizin Johannes Gutenberg Universität Mainz — Mainz
  • Dr. von Haunersches Kinderspital — Munich
Португалия · 2 центра
  • 2Ca Braga — Braga
  • Centro Hospitalar de Sao Joao - Hospital de Sao Joao — Porto
Австрия · 1 центр
  • Medizinische Universität Wien — Vienna
Нидерланды · 1 центр
  • Erasmus Medisch Centrum — Rotterdam

Идентификаторы

NCT: NCT04844606 · 16633 · I6T-MC-AMAZ · 2020-005311-49 · ISA-1 UC · ISA-2 CD · ISA-3 UC · ISA-4 CD

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗