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Phase 3 N=108 Treatment

Safety Study of Entocort for Children With Crohn's Disease

Crohn's Disease

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

OutcomeResultp-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
View full record on ClinicalTrials.gov →

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.

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