A Study to Evaluate the Efficacy of Guselkumab in Chinese Participants With Crohn's Disease (CD)

ConditionCrohn Disease
Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18+
SponsorXian-Janssen Pharmaceutical Ltd.

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 volunteers

Qualifiers

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

Design model

Single group

Treatments tested in this trial

  • Guselkumab (GUS)

    Drug

    Guselkumab will be administered intravenously or by subcutaneous injection.

Treatment groups

78 Participants
are divided into 1 treatment group
Group A: Guselkumab TreatmentExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

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.

Time frame
At Week 48

Secondary outcomes

1

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.

Time frame
At Weeks 12, 24 and 48
2

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.

Time frame
At Weeks 12 and 24
3

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.

Time frame
At Weeks 24 and 48
4

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.

Time frame
At Weeks 24 and 48

Other outcomes

Sponsors and contacts

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