Um estudo para saber mais sobre como o risankizumab funciona em jovens participantes com colite ulcerosa (MIGHTY)
Um estudo de fase 3, multicêntrico para avaliar a farmacocinética, a eficácia e a segurança do risankizumab com indução de etiqueta aberta, manutenção randomizada dupla e clínica e períodos de extensão de longo prazo em discos pediátricos (2 a 18 anos de idade) com colite ulcerativa severamente ativa severamente ativa
Ulcerative colitis (UC) is a type of inflammatory bowel disease that causes inflammation and bleeding from the lining of the rectum and colon (large intestine). This study will assess how Risankizumab moves through the body as well as how safe and effective it is in treating pediatric participants with moderate to severely active UC. Adverse events and change in disease activity will be assessed.
Risankizumab is an approved medication for moderate to severe UC in multiple countries and is being developed for the treatment of UC in pediatrics. This study is comprised of 3 cohorts that may participate in 3 substudies (SS). Cohort 1 will enroll participants with ages from 6 to less than 18 years. Cohort 2 will enroll participants with ages from 2 to less than 6 years. Cohort 3 will enroll participants with ages from 2 to less than 18 years. SS1 is an open-label induction period where participants will receive a weight-based induction regimen of risankizumab. SS2 is a double-blind maintenance period where participants will be randomized to receive 1 of 2 doses of weight-based maintenance regimen of risankizumab. SS3 is an open-label extension period where participants will receive risankizumab based off of their response in SS2. Around 120 pediatric participants with UC will be enrolled at around 80 sites worldwide.
Participants in SS1 will receive risankizumab intravenously during the 12-week induction period. Participants in SS2 will receive risankizumab subcutaneously during the 52-week randomized maintenance period. Participants in SS3 will receive risankizumab subcutaneously during the 208-week open label period. Participants will be followed-up for approximately 140 days.
There may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend regular visits during the study at a hospital or clinic. The effect of the treatment will be checked by medical assessments, blood tests, checking for side effects and completing questionnaires.
Visão geral do estudo
Status
Condições
Intervenção / Tratamento
Tipo de estudo
Inscrição (Estimado)
Estágio
- Fase 3
Contactos e Locais
Contato de estudo
- Nome: ABBVIE CALL CENTER
- Número de telefone: 844-663-3742
- E-mail: abbvieclinicaltrials@abbvie.com
Locais de estudo
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Brandenburg
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Cottbus, Brandenburg, Alemanha, 03048
- Recrutamento
- Medizinische Universitaet Lausitz - Carl Thiem /ID# 272023
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Hesse
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Kassel, Hesse, Alemanha, 34125
- Recrutamento
- Klinikum Kassel /ID# 271546
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North Rhine-Westphalia
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Münster, North Rhine-Westphalia, Alemanha, 48149
- Recrutamento
- Universitaetsklinikum Muenster /ID# 271898
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São Paulo, Brasil, 01308-050
- Recrutamento
- Hospital Sirio Libanes - Sao Paulo /ID# 271818
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Minas Gerais
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Juiz de Fora, Minas Gerais, Brasil, 36033-318
- Recrutamento
- Galileo Medical Research /ID# 271817
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Paraná
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Curitiba, Paraná, Brasil, 80250-060
- Recrutamento
- Hospital Pequeno Principe /ID# 271814
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Brussels, Bélgica, 1020
- Recrutamento
- Hospital Universite Enfants Reine Fabiola /ID# 271860
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Liège, Bélgica, 4000
- Recrutamento
- Centre Hospitalier Regional de la Citadelle /ID# 270459
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Brussels Capital
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Brussels, Brussels Capital, Bélgica, 1200
- Recrutamento
- Cliniques Universitaires UCL Saint-Luc /ID# 270123
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Alberta
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Calgary, Alberta, Canadá, T3B 6A8
- Recrutamento
- Alberta Children's Hospital /ID# 272635
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Edmonton, Alberta, Canadá, T6G 2B7
- Recrutamento
- University of Alberta Hospital /ID# 271168
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Ontario
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London, Ontario, Canadá, N6A 5W9
- Recrutamento
- London Health Sciences Centre - Verspeeten Family Cancer Centre /ID# 271157
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Guangdong
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Guangzhou, Guangdong, China, 510620
- Recrutamento
- Guangzhou Medical University Affiliated Women and Children's Medical Center /ID# 277962
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Henan
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Zhengzhou, Henan, China, 450018
- Recrutamento
- Henan Children's Hospital Zhengzhou Children's Hospital /ID# 278794
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Hunan
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Changsha, Hunan, China, 410007
- Recrutamento
- Hunan Children's Hospital /ID# 278111
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Jilin
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Changchun, Jilin, China, 130021
- Recrutamento
- The First Hospital of Jilin University - Changchun /ID# 279290
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Shanghai Municipality
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Shanghai, Shanghai Municipality, China, 200025
- Recrutamento
- Ruijin Hospital, Shanghai Jiaotong University School of Medicine /ID# 278113
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Zhejiang
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Hangzhou, Zhejiang, China, 310018
- Recrutamento
- Sir Run Run Shaw Hospital of Zhejiang University School of Medicine /ID# 277994
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Hangzhou, Zhejiang, China, 310056
- Recrutamento
- The Childrens Hospital of Zhejiang University School of Medicine /ID# 278815
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Gyeongsangnam-do
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Yangsan, Gyeongsangnam-do, Coréia do Sul, 50612
- Recrutamento
- Pusan National University Yangsan Hospital /ID# 272769
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Seoul Teugbyeolsi
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Seoul, Seoul Teugbyeolsi, Coréia do Sul, 03080
- Recrutamento
- Seoul National University Hospital /ID# 272852
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Seoul, Seoul Teugbyeolsi, Coréia do Sul, 06351
- Recrutamento
- Samsung Medical Center /ID# 272862
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Seoul, Seoul Teugbyeolsi, Coréia do Sul, 03181
- Recrutamento
- Kangbuk Samsung Hospital /ID# 273333
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Seoul, Seoul Teugbyeolsi, Coréia do Sul, 03722
- Recrutamento
- Yonsei University Health System - Severance Hospital /ID# 272894
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A Coruna
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A Coruña, A Coruna, Espanha, 15006
- Recrutamento
- Hospital Teresa Herrera - CHUAC /ID# 271459
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Madrid
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Majadahonda, Madrid, Espanha, 28222
- Recrutamento
- Hospital Universitario Puerta de Hierro - Majadahonda /ID# 271466
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Arizona
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Phoenix, Arizona, Estados Unidos, 85016
- Recrutamento
- Phoenix Children's Hospital /ID# 273015
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California
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San Diego, California, Estados Unidos, 92123
- Recrutamento
- Rady Children's Hospital /ID# 271873
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San Francisco, California, Estados Unidos, 94158
- Recrutamento
- University of California San Francisco - Mission Bay /ID# 273022
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Florida
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Miami, Florida, Estados Unidos, 33155
- Recrutamento
- Nicklaus Children's Hospital - Miami /ID# 271585
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Georgia
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Atlanta, Georgia, Estados Unidos, 30342
- Recrutamento
- Childrens Center For Digestive Health Care /ID# 273228
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Illinois
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Chicago, Illinois, Estados Unidos, 60637
- Recrutamento
- University of Chicago Medical Center /ID# 271588
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New Jersey
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Morristown, New Jersey, Estados Unidos, 07962
- Recrutamento
- Goryeb Children's Hospital /ID# 271801
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Ohio
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Cleveland, Ohio, Estados Unidos, 44106
- Recrutamento
- University Hospitals Cleveland Medical Center /ID# 271831
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Pennsylvania
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Philadelphia, Pennsylvania, Estados Unidos, 19104
- Recrutamento
- The Children's Hospital of Philadelphia /ID# 273222
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Pittsburgh, Pennsylvania, Estados Unidos, 15224
- Recrutamento
- Upmc Children'S Hospital Of Pittsburgh /ID# 272328
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South Carolina
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Greenville, South Carolina, Estados Unidos, 29615
- Recrutamento
- Patewood Medical Campus /ID# 272477
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Texas
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Dallas, Texas, Estados Unidos, 75235
- Recrutamento
- University of Texas - Southwestern Medical Center /ID# 271835
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Thessaloniki, Grécia, 54642
- Recrutamento
- General Hospital of Thessaloniki Hippokrateio /ID# 271939
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Attica
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Athens, Attica, Grécia, 11527
- Recrutamento
- Thoracic General Hospital of Athens I Sotiria /ID# 270143
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Chaïdári, Attica, Grécia, 12462
- Recrutamento
- University General Hospital Attikon /ID# 272361
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Trieste, Itália, 34137
- Recrutamento
- Ospedale Infantile Burlo Garofolo /ID# 274442
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Foggia
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San Giovanni Rotondo, Foggia, Itália, 71013
- Recrutamento
- Fondazione di Religione e di Culto Casa Sollievo della Sofferenza /ID# 271889
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Napoli
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Naples, Napoli, Itália, 80131
- Recrutamento
- Azienda Ospedaliera Universitaria Federico II - Naples /ID# 271895
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Roma
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Rome, Roma, Itália, 00168
- Recrutamento
- Fondazione Policlinico Universitario Agostino Gemelli IRCCS-Universita Cattolica /ID# 272967
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Fukushima, Japão, 960-1295
- Recrutamento
- Fukushima Medical University Hospital /ID# 281178
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Aichi-ken
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Ōbu, Aichi-ken, Japão, 474-8710
- Recrutamento
- Aichi Children's Health And Medical Center /ID# 280462
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Chiba
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Kashiwa-shi, Chiba, Japão, 277-0871
- Recrutamento
- Tsujinaka Hospital - Kashiwanoha /ID# 280303
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Fukuoka
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Kurume-shi, Fukuoka, Japão, 830-0011
- Recrutamento
- Kurume University Hospital /ID# 280792
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Gunma
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Maebashi, Gunma, Japão, 371-8511
- Recrutamento
- Gunma University Hospital /ID# 281179
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Hyōgo
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Kobe, Hyōgo, Japão, 650-0017
- Recrutamento
- Kobe University Hospital /ID# 281796
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Kumamoto
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Kumamoto, Kumamoto, Japão, 861-8520
- Recrutamento
- Japanese Red Cross Kumamoto Hospital /ID# 280696
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Saga-ken
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Saga, Saga-ken, Japão, 849-8501
- Recrutamento
- Saga University Hospital /ID# 281232
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Saitama
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Saitama-shi, Saitama, Japão, 330-8777
- Recrutamento
- Saitama Children's Medical Center /ID# 280603
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Shizuoka
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Hamamatsu, Shizuoka, Japão, 431-3192
- Recrutamento
- Hamamatsu University Hospital /ID# 281614
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Tokyo
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Bunkyo-ku, Tokyo, Japão, 113-8519
- Recrutamento
- Institute of Science Tokyo Hospital /ID# 280694
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Bunkyo-ku, Tokyo, Japão, 113-8431
- Recrutamento
- Juntendo University Hospital /ID# 280463
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Fuchu-shi, Tokyo, Japão, 183-8561
- Recrutamento
- Tokyo Metropolitan Children's Medical Center /ID# 280791
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Setagaya City, Tokyo, Japão, 157-8535
- Recrutamento
- National Center For Child Health And Development /ID# 280460
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Masovian Voivodeship
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Warsaw, Masovian Voivodeship, Polônia, 00-189
- Recrutamento
- Centrum Zdrowia Mdm /ID# 276942
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Warsaw, Masovian Voivodeship, Polônia, 00-728
- Recrutamento
- Medical Network Sp. z o.o. /ID# 276903
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Podlaskie Voivodeship
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Bialystok, Podlaskie Voivodeship, Polônia, 15-274
- Recrutamento
- Uniwersytecki Dzieciecy Szpital Kliniczny im. L. Zamenhofa w Bialymstoku /ID# 276771
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Liverpool, Reino Unido, L12 2AP
- Recrutamento
- Alder Hey Children's NHS Foundation Trust /ID# 271533
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Cambridgeshire
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Cambridge, Cambridgeshire, Reino Unido, CB2 2QQ
- Recrutamento
- Addenbrookes Hospital /ID# 271489
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England
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Sheffield, England, Reino Unido, S10 2TH
- Recrutamento
- Sheffield Children's Hospital NHS Foundation Trust /ID# 271490
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Stockholm County
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Solna, Stockholm County, Suécia, 171 64
- Recrutamento
- Karolinska University Hospital Solna /ID# 271679
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Stockholm, Stockholm County, Suécia, 118 83
- Recrutamento
- Sodersjukhuset /ID# 271678
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Västra Götaland County
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Gothenburg, Västra Götaland County, Suécia, 413 46
- Recrutamento
- Sahlgrenska Universitetssjukhuset /ID# 271675
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Contato:
- Site Coordinator
- Número de telefone: +46313435865
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Novi Sad, Sérvia, 21000
- Recrutamento
- Institute for Child and Youth Health Care of Vojvodina /ID# 269961
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Beograd
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Belgrade, Beograd, Sérvia, 11000
- Recrutamento
- University Children's Hospital /ID# 269960
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Belgrade-Vračar, Beograd, Sérvia, 11000
- Recrutamento
- Institut za zdravstvenu zastitu majke i deteta Srbije Dr Vukan Cupic /ID# 270696
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Taichung, Taiwan, 407219
- Recrutamento
- Taichung Veterans General Hospital /ID# 269242
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Taipei, Taiwan, 100
- Recrutamento
- National Taiwan University Hospital /ID# 269244
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Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
Aceita Voluntários Saudáveis
Gêneros Elegíveis para o Estudo
Descrição
Inclusion Criteria:
- Active ulcerative colitis (UC) with an modified Mayo Score (mMS) of 5 to 9 points and endoscopic subscore of 2 to 3 (confirmed by central reader).
- Demonstrated intolerance or inadequate response (IR) to one or more of the following categories of drugs:
aminosalicylates (except in countries where failure of this drug class is not sufficient for eligibility), oral locally acting corticosteroids, systemic steroids (prednisone or equivalent), immunomodulators (IMMs), and/or biologic therapies, as outlined in the protocol.
- Subjects must have a documented history of UC for at least 3 months prior to Baseline, confirmed by colonoscopy during the screening period, with exclusion of current infection, colonic dysplasia and/or malignancy. Documentation of pathology results consistent with the diagnosis of UC must be available.
Exclusion Criteria:
- Participants who have had a major surgery performed within 12 weeks prior to Baseline or planned during the conduct of the study (e.g., inguinal hernia repair, cholecystectomy, intestinal resection).
- Participants who have concurrent clinically significant medical conditions other than the indication being studied or any other reason that the investigator determines would interfere with the subject's participation in this study, would make the subject an unsuitable candidate to receive study treatment, or would put the subject at risk by participating in the study.
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: Randomizado
- Modelo Intervencional: Atribuição sequencial
- Mascaramento: Dobro
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
Experimental: PK Cohort 1: SS1
Cohort 1 will consist of 2 age groups (6 to < 12 years and 12 to < 18 years). SS1 is a 12-week induction period where participants will receive a weight-based dose of risankizumab. All participants who complete SS1 are eligible to enter SS2 |
Risankizumab intravenous (IV) infusion
Outros nomes:
Risankizumab subcutaneous (SC) injection
Outros nomes:
|
|
Experimental: PK Cohort 1: SS2 Dose A
Cohort 1 will consist of 2 age groups (6 to < 12 years and 12 to < 18 years). Participants who complete SS1 will be randomized into a 52-week maintenance phase (SS2) to receive double-blind risankizumab Dose A. Participants who complete SS2 will have the opportunity to enter the open-label long term extension SS3. |
Risankizumab intravenous (IV) infusion
Outros nomes:
Risankizumab subcutaneous (SC) injection
Outros nomes:
|
|
Experimental: PK Cohort 1: SS2 Dose B
Cohort 1 will consist of 2 age groups (6 to < 12 years and 12 to < 18 years). Participants who complete SS1 will be randomized into a 52-week maintenance phase (SS2) to receive double-blind risankizumab Dose B. Participants who complete SS2 will have the opportunity to enter the open-label long term extension SS3. |
Risankizumab intravenous (IV) infusion
Outros nomes:
Risankizumab subcutaneous (SC) injection
Outros nomes:
|
|
Experimental: PK Cohort 1: SS3 Dose A
Cohort 1 will consist of 2 age groups (6 to < 12 years and 12 to < 18 years). SS3 is a 208-week extension period where participants receive risankizumab based on their response in SS2. |
Risankizumab intravenous (IV) infusion
Outros nomes:
Risankizumab subcutaneous (SC) injection
Outros nomes:
|
|
Experimental: PK Cohort 1: SS3 Dose B
Cohort 1 will consist of 2 age groups (6 to < 12 years and 12 to < 18 years). SS3 is a 208-week extension period where participants receive risankizumab based on their response in SS2. |
Risankizumab intravenous (IV) infusion
Outros nomes:
Risankizumab subcutaneous (SC) injection
Outros nomes:
|
|
Experimental: PK Cohort 2: SS1
Cohort 2 will enroll participants aged 2 to less than 6 years. SS1 is a 12-week induction period where participants will receive a weight-based dose of risankizumab. All subjects who complete SS1 are eligible to enter SS2. |
Risankizumab intravenous (IV) infusion
Outros nomes:
Risankizumab subcutaneous (SC) injection
Outros nomes:
|
|
Experimental: PK Cohort 2: SS2 Dose A
Cohort 2 will enroll participants aged 2 to less than 6 years. Participants who complete SS1 will be randomized into a 52-week maintenance phase (SS2) to receive double-blind risankizumab Dose A. Participants who complete SS2 will have the opportunity to enter the open-label long-term extension SS3. |
Risankizumab intravenous (IV) infusion
Outros nomes:
Risankizumab subcutaneous (SC) injection
Outros nomes:
|
|
Experimental: PK Cohort 2: SS2 Dose B
Cohort 2 will enroll participants aged 2 to less than 6 years. Participants who complete SS1 will be randomized into a 52-week maintenance phase (SS2) to receive double-blind risankizumab Dose B. Participants who complete SS2 will have the opportunity to enter the open-label long-term extension SS3. |
Risankizumab intravenous (IV) infusion
Outros nomes:
Risankizumab subcutaneous (SC) injection
Outros nomes:
|
|
Experimental: PK Cohort 2: SS3 Dose A
Cohort 2 will enroll participants aged 2 to less than 6 years. SS3 is a 208-week extension period where participants receive risankizumab based on their response in SS2. |
Risankizumab intravenous (IV) infusion
Outros nomes:
Risankizumab subcutaneous (SC) injection
Outros nomes:
|
|
Experimental: PK Cohort 2: SS3 Dose B
Cohort 2 will enroll participants aged 2 to less than 6 years. SS3 is a 208-week extension period where participants receive risankizumab based on their response in SS2. |
Risankizumab intravenous (IV) infusion
Outros nomes:
Risankizumab subcutaneous (SC) injection
Outros nomes:
|
|
Experimental: Expansion Cohort 3: SS1
Cohort 3 will enroll participants aged 2 to less than 18 years. SS1 is a 12-week induction period where participants will receive a weight-based dose of risankizumab. All participants who complete SS1 are eligible to enter SS2. |
Risankizumab intravenous (IV) infusion
Outros nomes:
Risankizumab subcutaneous (SC) injection
Outros nomes:
|
|
Experimental: Expansion Cohort 3: SS2 Dose A
Cohort 3 will enroll participants aged 2 to less than 18 years. Participants who complete SS1 will be randomized into a 52-week maintenance phase (SS2) to receive double-blind risankizumab Dose A. Participants who complete SS2 will have the opportunity to enter the open-label long term extension SS3. |
Risankizumab intravenous (IV) infusion
Outros nomes:
Risankizumab subcutaneous (SC) injection
Outros nomes:
|
|
Experimental: Expansion Cohort 3: SS2 Dose B
Cohort 3 will enroll participants aged 2 to less than 18 years. Participants who complete SS1 will be randomized into a 52-week maintenance phase (SS2) to receive double-blind risankizumab Dose B. Participants who complete SS2 will have the opportunity to enter the open-label long term extension SS3. |
Risankizumab intravenous (IV) infusion
Outros nomes:
Risankizumab subcutaneous (SC) injection
Outros nomes:
|
|
Experimental: Expansion Cohort 3: SS3 Dose A
Cohort 3 will enroll participants aged 2 to less than 18 years. SS3 is a 208-week extension period where participants receive risankizumab based on their response in SS2. |
Risankizumab intravenous (IV) infusion
Outros nomes:
Risankizumab subcutaneous (SC) injection
Outros nomes:
|
|
Experimental: Expansion Cohort 3: SS3 Dose B
Cohort 3 will enroll participants aged 2 to less than 18 years. SS3 is a 208-week extension period where participants receive risankizumab based on their response in SS2. |
Risankizumab intravenous (IV) infusion
Outros nomes:
Risankizumab subcutaneous (SC) injection
Outros nomes:
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
PK Lead-In Cohort 1: Maximum Observed Serum Concentration (Cmax)
Prazo: At Week 64
|
Maximum observed plasma concentration (Cmax) |
At Week 64
|
|
PK Lead-In Cohort 2: Maximum Observed Serum Concentration (Cmax)
Prazo: At Week 64
|
Maximum observed plasma concentration (Cmax) |
At Week 64
|
|
PK Lead-In Cohort 1: Time to Maximum Serum Concentration (Tmax)
Prazo: At Week 64
|
Time to maximum plasma concentration (Tmax) |
At Week 64
|
|
PK Lead-In Cohort 2: Time to Maximum Serum Concentration (Tmax)
Prazo: At Week 64
|
Time to maximum plasma concentration (Tmax) |
At Week 64
|
|
PK Lead-In Cohort 1: Area Under the Serum Concentration-Time Curve Over the Dosing Interval (AUCtau)
Prazo: At Week 64
|
Area under the serum concentration-time curve over the dosing interval (AUCtau) |
At Week 64
|
|
PK Lead-In Cohort 2: Area Under the Serum Concentration-Time Curve Over the Dosing Interval (AUCtau)
Prazo: At Week 64
|
Area under the serum concentration-time curve over the dosing interval (AUCtau) |
At Week 64
|
|
Expansion Cohort 3: Achievement of Clinical Remission per Modified Mayo Score (mMS) Among Week 12 Clinical Responders per mMS
Prazo: At Week 64
|
Clinical remission on the mMS is defined as defined as Stool Frequency Subscore (SFS) ≤ 1 and not greater than Baseline, Rectal Bleeding Subscore (RBS) = 0, and Mayo Endoscopic Subscore (MES) ≤ 1 |
At Week 64
|
|
Number of Participants With Adverse Events
Prazo: Up to 292 Weeks
|
An adverse event (AE) is defined as any untoward medical occurrence in a patient or clinical investigation subject administered a pharmaceutical product and which does not necessarily have a causal relationship with this treatment. The investigator assessed the relationship of each event to the use of study drug as either probably related, possibly related, probably not related or not related |
Up to 292 Weeks
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Coorte de expansão 3: Realização de remissão clínica por mms
Prazo: Na semana 12
|
Na semana 12
|
|
|
Coorte de expansão 3: Realização da resposta clínica por MMS
Prazo: Na semana 12
|
Na semana 12
|
|
|
Coorte de expansão 3: Realização da melhoria endoscópica
Prazo: Na semana 12
|
Na semana 12
|
|
|
Coorte de expansão 3: Resposta sintomática por MMS parcial
Prazo: Na semana 12
|
Na semana 12
|
|
|
Coorte de expansão 3: Realização da resposta clínica por MMS entre a semana 12 respondedores por mms
Prazo: Na semana 64
|
Na semana 64
|
|
|
Coorte de expansão 3: Realização da melhoria endoscópica entre os respondedores da semana 12 por MMS
Prazo: Na semana 64
|
Na semana 64
|
|
|
Coorte de expansão 3: Realização de remissão clínica livre de corticosteróides por MMS entre os respondedores da semana 12 por MMS
Prazo: Na semana 64
|
Na semana 64
|
|
|
PK Lead-In Cohort 1: Achievement of corticosteroid-free (at least 90 days without corticosteroid exposure) clinical remission per mMS at Week 64 among Week 12 responders per mMS
Prazo: Up to Week 64
|
Up to Week 64
|
|
|
PK Lead-In Cohort 2: Achievement of corticosteroid-free (at least 90 days without corticosteroid exposure) clinical remission per mMS at Week 64 among Week 12 responders per mMS
Prazo: Up to Week 64
|
Up to Week 64
|
|
|
PK Lead-In Cohort 1: Achievement of clinical remission per mMS among Week 12 responders per mMS
Prazo: At Week 64
|
Clinical remission on the mMS is defined as defined as Stool Frequency Subscore (SFS) ≤ 1 and not greater than Baseline, Rectal Bleeding Subscore (RBS) = 0, and Mayo Endoscopic Subscore (MES) ≤ 1 |
At Week 64
|
|
PK Lead-In Cohort 2: Achievement of clinical remission per mMS among Week 12 responders per mMS
Prazo: At Week 64
|
Clinical remission on the mMS is defined as defined as Stool Frequency Subscore (SFS) ≤ 1 and not greater than Baseline, Rectal Bleeding Subscore (RBS) = 0, and Mayo Endoscopic Subscore (MES) ≤ 1 |
At Week 64
|
|
PK Lead-In Cohort 1: Achievement of clinical remission per mMS
Prazo: At Week 12
|
Clinical remission on the mMS is defined as Stool Frequency Subscore (SFS) ≤ 1 and not greater than Baseline, Rectal Bleeding Subscore (RBS) = 0, and Mayo Endoscopic Subscore (MES) ≤ 1 |
At Week 12
|
|
PK Lead-In Cohort 2: Achievement of clinical remission per mMS
Prazo: At Week 12
|
Clinical remission on the mMS is defined as Stool Frequency Subscore (SFS) ≤ 1 and not greater than Baseline, Rectal Bleeding Subscore (RBS) = 0, and Mayo Endoscopic Subscore (MES) ≤ 1 |
At Week 12
|
|
PK Lead-In Cohort 1: Achievement of clinical response per mMS
Prazo: At Week 12
|
Clinical response per mMS is defined as decrease in mMS by ≥ 2 points and ≥ 30% from Baseline with a decrease in Rectal Bleeding Subscore (RBS) of ≥ 1 or an absolute RBS of 0 or 1. |
At Week 12
|
|
PK Lead-In Cohort 2: Achievement of clinical response per mMS
Prazo: At Week 12
|
Clinical response per mMS is defined as decrease in mMS by ≥ 2 points and ≥ 30% from Baseline with a decrease in Rectal Bleeding Subscore (RBS) of ≥ 1 or an absolute RBS of 0 or 1. |
At Week 12
|
|
PK Lead-In Cohort 1: Achievement of endoscopic improvement
Prazo: At Week 12
|
Endoscopic improvement defined as MES ≤ 1 |
At Week 12
|
|
PK Lead-In Cohort 2: Achievement of endoscopic improvement
Prazo: At Week 12
|
Endoscopic improvement defined as MES ≤ 1 |
At Week 12
|
|
PK Lead-In Cohort 1: Symptomatic response per partial mMS
Prazo: At Week 12
|
Symptomatic response per partial mMS is defined as decrease in partial mMS by ≥ 1 points and ≥ 30% from Baseline with decrease in RBS of ≥ 1 or an absolute RBS of 0 or 1. |
At Week 12
|
|
PK Lead-In Cohort 2: Symptomatic response per partial mMS
Prazo: At Week 12
|
Symptomatic response per partial mMS is defined as decrease in partial mMS by ≥ 1 points and ≥ 30% from Baseline with decrease in RBS of ≥ 1 or an absolute RBS of 0 or 1. |
At Week 12
|
|
PK Lead-In Cohort 1: Achievement of clinical response per mMS among Week 12 responders per mMS
Prazo: At Week 64
|
Clinical response per mMS is defined as decrease in mMS by ≥ 2 points and ≥ 30% from Baseline with a decrease in Rectal Bleeding Subscore (RBS) of ≥ 1 or an absolute RBS of 0 or 1. |
At Week 64
|
|
PK Lead-In Cohort 2: Achievement of clinical response per mMS among Week 12 responders per mMS
Prazo: At Week 64
|
Clinical response per mMS is defined as decrease in mMS by ≥ 2 points and ≥ 30% from Baseline with a decrease in Rectal Bleeding Subscore (RBS) of ≥ 1 or an absolute RBS of 0 or 1. |
At Week 64
|
|
PK Lead-In Cohort 1: Achievement of endoscopic improvement among Week 12 responders per mMS
Prazo: At Week 64
|
Endoscopic improvement defined as MES ≤ 1 |
At Week 64
|
|
PK Lead-In Cohort 2: Achievement of endoscopic improvement among Week 12 responders per mMS
Prazo: At Week 64
|
Endoscopic improvement defined as MES ≤ 1 |
At Week 64
|
Colaboradores e Investigadores
Patrocinador
Investigadores
- Diretor de estudo: ABBVIE INC., AbbVie
Publicações e links úteis
Links úteis
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Real)
Conclusão Primária (Estimado)
Conclusão do estudo (Estimado)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- M19-751
- 2024-514695-41-00 (Ctis)
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
Descrição do plano IPD
AbbVie is committed to responsible clinical trial data sharing. This includes access to anonymized, individual and trial-level data (analysis data sets), as well as other information.
Prazo de Compartilhamento de IPD
For details on when studies are available for sharing, visit https://vivli.org/ourmember/abbvie/
Critérios de acesso de compartilhamento IPD
To learn more about the process, or to submit a request, visit the following link https://www.abbvieclinicaltrials.com/hcp/data-sharing/
Tipo de informação de suporte de compartilhamento de IPD
- PROTOCOLO DE ESTUDO
- SEIVA
Informações sobre medicamentos e dispositivos, documentos de estudo
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produto fabricado e exportado dos EUA
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