Phase 3
N=108
Safety Study of Entocort for Children With Crohn's Disease
Crohn's Disease
Bottom Line
View on ClinicalTrials.gov: NCT01444092 ↗Enrolled (actual)
108
Serious AEs
7.4%
Results posted
Aug 2016
Primary outcome: Primary: Adverse Event — 79 Patients
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 3
- Interventions
- Entocort (Drug)
- Age
- Pediatric · 5+ yrs
- Sex
- All
- Sponsor
- Padagis LLC
- Primary completion
- Sep 2014
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Adverse Event |
79 | — |
| SECONDARY PCDAI |
19.10; -10.0 | — |
| SECONDARY IMPACT 3 |
132.1; 7.8 | — |
Summary
A Safety Study using Entocort EC for children with mild to moderate Crohn's Disease
Eligibility Criteria
Inclusion Criteria
- All male and female subjects must be aged 5 to 17, inclusive, and must not have reached their 18th birthday by the estimated final office visit.
- Subject must be diagnosed with active Crohn's disease of the ileum and/or ascending colon confirmed by endoscopic and/or radiographic evidence, and/or evidence of mucosal erosions and/or histology.
- Subjects with mild to moderate Crohn's disease.
- All subjects must have a stool analysis negative for Clostridium difficile toxin, Yersinia enterolytica, Campylobacter jejuni, Salmonella, Shigella, within the 30 days prior to visit 1.
- All subjects must have had laboratory assessments within 7 days prior to visit 1.
- All subjects must weigh >= 15 kg at time of enrollment
Exclusion Criteria
- Subjects who have had any previous intestinal resection proximal to and including the ascending colon
- Subjects with evidence of severe active Crohn's disease and/or, stricturing and prestenotic dilatation, clinical evidence of obstruction, perirectal abscess, perirectal disease with active draining fistulas, perforation, or any septic complications
- Subjects who do not have a negative stool analysis, within the 30 days prior to visit 1
- Subjects who have been screened/or enrolled in this study previously within the last 30 days
- Subjects with morning cortisol level <150 nmol/l (5.4 ug/dl) or DHEA-S below normal range for age and gender
Data sourced from ClinicalTrials.gov (NCT01444092). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.