The Efficacy of Open Label Infliximab for the Induction and Maintenance of Mucosal Healing in Small Bowel Crohn's Disease Assessed Through Wireless Camera Endoscopy (ICE)
Primary Purpose
Crohn's Disease
Status
Completed
Phase
Phase 4
Locations
Canada
Study Type
Interventional
Intervention
Infliximab 5 mg/kg body weight infused over 2 hours
Sponsored by
About this trial
This is an interventional treatment trial for Crohn's Disease focused on measuring Crohn's Disease, infliximab, capsule endoscopy
Eligibility Criteria
Inclusion Criteria:
- 18 years old
- Established diagnosis of Crohn's disease and evidence of small bowel involvement
- CDAI score between 220 and 450 inclusively
- Lewis score of at least 790 at Screening
- Colonoscopy within the last 6 months
- Successful excretion of the intact patency capsule Exclusion Criteria
- Contraindications to anti-TNF therapy (TB, cardiac impairment, etc.)
- Prior bowel resection
- Prior anti-TNF exposure
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Infliximab infusions (5 mg/kg) at weeks 0, 2, 6, 14 and 22
Arm Description
Outcomes
Primary Outcome Measures
Endoscopic Improvement
Mean change in Lewis score between Baseline and Week 26
Secondary Outcome Measures
Clinical improvement
Mean change in Crohn's Disease Activity Index (CDAI) between Baseline and Week 26.
Early endoscopic improvement
Mean change in Lewis score between Baseline and Week 10
Clinical Improvement
Mean change in CDAI between Baseline and Week 10
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01181765
Brief Title
The Efficacy of Open Label Infliximab for the Induction and Maintenance of Mucosal Healing in Small Bowel Crohn's Disease Assessed Through Wireless Camera Endoscopy
Acronym
ICE
Official Title
The Efficacy of Open Label Infliximab for the Induction and Maintenance of Mucosal Healing in Small Bowel Crohn's Disease Assessed Through Wireless Camera Endoscopy (the ICE Study)
Study Type
Interventional
2. Study Status
Record Verification Date
December 2013
Overall Recruitment Status
Completed
Study Start Date
June 2012 (undefined)
Primary Completion Date
January 2013 (Actual)
Study Completion Date
January 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Janssen Inc.
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This is a pilot study to estimate the efficacy of infliximab in inducing and maintaining healing of lesions in the mucosa of subjects with Crohn's disease involving their small bowel.
Detailed Description
Landmark trials in Crohn's disease demonstrated the efficacy of infliximab in inducing and maintaining clinical remission. Furthermore, the endoscopic sub-studies within these trials demonstrated the ability of infliximab to rapidly induce and maintain mucosal healing as evidenced by the complete absence of mucosal breaks in the colon and terminal ileum. Unfortunately, conventional colonoscopy does not allow intestinal exploration beyond a very restricted portion of the small bowel (at most 10-15 cm of the terminal ileum). A study that systematically examines the changes in the small bowel mucosa during Crohn's disease symptomatic improvement is clearly needed.
This study consists of 20 subjects and 30 weeks of follow up. All subjects will undergo wireless camera endoscopy at three (3) visits, namely: at Screening, at Week 10 and at Week 26. Infliximab is administered at (5) visits, namely: at Baseline (week 0), Week 2, Week 6, Week 14 and Week 22. In some subjects, an ileal-colonoscopy may be performed at Week 26.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Crohn's Disease
Keywords
Crohn's Disease, infliximab, capsule endoscopy
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
1 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Infliximab infusions (5 mg/kg) at weeks 0, 2, 6, 14 and 22
Arm Type
Experimental
Intervention Type
Biological
Intervention Name(s)
Infliximab 5 mg/kg body weight infused over 2 hours
Intervention Description
Subjects will receive IV Infusion of infliximab 5 mg/kg body weight at Week 0, Week 2, Week 6, Week 14 and Week 22 as per the approved Canadian product monograph of infliximab.
Primary Outcome Measure Information:
Title
Endoscopic Improvement
Description
Mean change in Lewis score between Baseline and Week 26
Time Frame
Week 26
Secondary Outcome Measure Information:
Title
Clinical improvement
Description
Mean change in Crohn's Disease Activity Index (CDAI) between Baseline and Week 26.
Time Frame
Week 26
Title
Early endoscopic improvement
Description
Mean change in Lewis score between Baseline and Week 10
Time Frame
Week 10
Title
Clinical Improvement
Description
Mean change in CDAI between Baseline and Week 10
Time Frame
Week 10
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
18 years old
Established diagnosis of Crohn's disease and evidence of small bowel involvement
CDAI score between 220 and 450 inclusively
Lewis score of at least 790 at Screening
Colonoscopy within the last 6 months
Successful excretion of the intact patency capsule Exclusion Criteria
Contraindications to anti-TNF therapy (TB, cardiac impairment, etc.)
Prior bowel resection
Prior anti-TNF exposure
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Janssen Inc. Clinical Trial
Organizational Affiliation
Janssen Inc.
Official's Role
Study Director
Facility Information:
City
Ottawa
State/Province
Ontario
Country
Canada
City
Toronto
State/Province
Ontario
Country
Canada
12. IPD Sharing Statement
Links:
URL
http://filehosting.pharmacm.com/DownloadService.ashx?client=CTR_JNJ_6051&studyid=3412&filename=CR100747_CSR.PDF
Description
The Efficacy of Open-Label Infliximab for the Induction and Maintenance of Mucosal Healing in Small Bowel Crohn's Disease Assessed Through Wireless Camera Endoscopy (the ICE study).
Learn more about this trial
The Efficacy of Open Label Infliximab for the Induction and Maintenance of Mucosal Healing in Small Bowel Crohn's Disease Assessed Through Wireless Camera Endoscopy
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