This will be a randomised, double blind, placebo controlled, parallel group evaluation of the effect of OC000459 given orally for eight weeks on active eosinophilic esophagitis.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
26
Swiss EoE Research Group
Olten, Switzerland
Effect of OC000459 on eosinophil load of the esophageal tissue
Time frame: 8 weeks
Effect of OC000459 on clinical manifestations of EoE
Time frame: 8 weeks
Effect of OC000459 on endoscopic alterations
Time frame: 8 weeks
Effect of OC000459 on EoE related blood and tissue biomarkers
Time frame: 8 weeks
Safety and tolerability of OC000459 in patients with active EoE
Time frame: 8 weeks
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