About this trial
The purpose of this study is to evaluate how well guselkumab works in participants with Crohn's disease (CD; a long-term condition causing severe inflammation of the intestinal tract) who no longer respond to treatment with ustekinumab.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Has a confirmed diagnosis of Crohn's disease (CD)
Diagnosed with active CD, as defined by baseline Crohn's Disease Activity Index (CDAI) score greater than or equal to (>=) 220
Participants had received the ustekinumab (UST) induction phase and received maintenance therapy via subcutaneous (SC) injection every 8 weeks or every 12 weeks
Initially responded to UST induction therapy and then lose response to UST
Disqualifiers
Received UST dose optimization or multiple intravenous therapy in maintenance phase
Participants with CD requiring urgent surgical or endoscopic intervention, or requiring elective surgery within 2 months
Is currently enrolled in an interventional clinical study
Complications of CD, such as symptomatic strictures or stenoses, short gut syndrome
Trial design
Single group
Treatments tested in this trial
Guselkumab (GUS)
DrugGuselkumab will be administered intravenously or by subcutaneous injection.
Treatment groups
Trial outcomes
Primary outcomes
Percentage of Participants Achieving Clinical Remission At Week 48
Clinical remission is defined as less than (\<) 150-point reduction in Crohn's Disease Activity Index (CDAI) score. The CDAI is a validated multi-item measure of severity of illness derived as a weighted sum of 8 different Crohn's disease-related variables. The CDAI score was assessed by collecting information on 8 different Crohn's disease-related variables: extra-intestinal manifestations, abdominal mass, weight, hematocrit, total number of liquid stools, abdominal pain/cramping, use of antidiarrheal drug(s), and/or opiates, and general well-being. In general, CDAI score ranges from 0 to approximately 600; higher score indicates higher disease activities.
Secondary outcomes
Percentage of Participants Achieving Clinical Response At Weeks 12, 24 and 48
Clinical response is defined as greater than or equal to (\>=) 100-point reduction from baseline in CDAI score. The CDAI is a validated multi-item measure of severity of illness derived as a weighted sum of 8 different Crohn's disease-related variables. The CDAI score was assessed by collecting information on 8 different Crohn's disease-related variables: extra-intestinal manifestations, abdominal mass, weight, hematocrit, total number of liquid stools, abdominal pain/cramping, use of antidiarrheal drug(s), and/or opiates, and general well-being. In general, CDAI score ranges from 0 to approximately 600; higher score indicates higher disease activities.
Percentage of Participants Achieving Clinical Remission At Weeks 12 and 24
Clinical remission is defined as \< 150-point reduction in CDAI score. The CDAI is a validated multi-item measure of severity of illness derived as a weighted sum of 8 different Crohn's disease-related variables. The CDAI score was assessed by collecting information on 8 different Crohn's disease-related variables: extra-intestinal manifestations, abdominal mass, weight, hematocrit, total number of liquid stools, abdominal pain/cramping, use of antidiarrheal drug(s), and/or opiates, and general well-being. In general, CDAI score ranges from 0 to approximately 600; higher score indicates higher disease activities.
Percentage of Participants Achieving Endoscopic Response
Endoscopic response is defined as \>= 50% improvement from baseline in Simple Endoscopic Score for Crohn's Disease (SES-CD) score. The SES-CD is based on the evaluation of 4 variables: (ulcers - scored according to size, proportion of the surface covered by ulcers according to extent, proportion of affected surface with any other lesions according to extent, stenosis \[single or multiple, and whether the colonoscopy could pass through the narrow lumen\]), each considered in 5 segments of the bowel (the ileum, ascending colon, transverse colon, descending colon, and rectum). An overall total SES-CD score is derived from the sum of all the component scores and can range from 0 to 60. Higher scores indicating severe disease.
Percentage of Participants Achieving Endoscopic Remission
Endoscopic remission is defined as SES-CD less than or equal to (\<=) 2 in any individual component. The SES-CD is based on the evaluation of 4 variables: (ulcers - scored according to size, proportion of the surface covered by ulcers according to extent, proportion of affected surface with any other lesions according to extent, stenosis \[single or multiple, and whether the colonoscopy could pass through the narrow lumen\]), each considered in 5 segments of the bowel (the ileum, ascending colon, transverse colon, descending colon, and rectum). An overall total SES-CD score is derived from the sum of all the component scores and can range from 0 to 60. Higher scores indicating severe disease.
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