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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 13 December 2021
Main ID:  NCT00035503
Date of registration: 03/05/2002
Prospective Registration: No
Primary sponsor: Teva Branded Pharmaceutical Products R&D, Inc.
Public title: Multicenter Trial For Patients With Acute Crohn's Disease
Scientific title:
Date of first enrolment: January 31, 2002
Target sample size:
Recruitment status: Completed
URL:  https://clinicaltrials.gov/show/NCT00035503
Study type:  Interventional
Study design:  Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: Double.  
Phase:  Phase 2
Countries of recruitment
Canada United States
Contacts
Key inclusion & exclusion criteria

- Must have active confirmed Crohn's disease with CDAI > 220 and < 400.

- Otherwise healthy.



Age minimum: 18 Years
Age maximum: N/A
Gender: All
Health Condition(s) or Problem(s) studied
Crohn's Disease
Intervention(s)
Drug: etiprednol dicloacetate
Primary Outcome(s)
Secondary Outcome(s)
Secondary ID(s)
IXR-201-19-166
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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