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Phase 2 N=14 Double-blind Treatment

Oral Administration of AlequelTM for Patients With Inflammatory Bowel Disease (IBD)

Crohn's Disease

Enrolled (actual)
14
Serious AEs
0.0%
Results posted
Sep 2014
Primary outcome: Primary: Number of Participants With Improved in Disease Activity — 0 participants

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Alequel (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Hadassah Medical Organization
Primary completion
Jan 2010

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants With Improved in Disease Activity

Summary

Oral administration of Alequel, a mixture of proteins derived from the patient's bowel will be tested in patients with inflammatory bowel disease.

Eligibility Criteria

Inclusion Criteria

  • Crohn's disease

Exclusion Criteria

  • Immune suppression
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02185183). 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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