Center for Digestive Diseases Eppendorf
Hamburg, 20249, Germany
NCT Number: NCT02493335
The purpose of this study is to prove the superiority of a 48-weeks treatment with budesonide orodispersible tablets versus placebo for the maintenance of clinico-pathological remission in patients with eosinophilic esophagitis.
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Notify Me18 year–75 year
All sexes
Interventional
Phase 3
Hamburg, 20249, Germany
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Other names: BUL 0.5mg BID
Other names: BUL 1mg BID
Other names: Placebo BID
Time frame: 48 weeks
Time frame: 48 weeks
Time frame: 48 weeks
Dr. Falk Pharma GmbH
Industry
Double-blind, Randomized, Placebo-controlled, Phase III Study on the Efficacy and Tolerability of a 48-week Treatment With Two Different Doses of Budesonide Effervescent Tablets vs. Placebo for Maintenance of Clinico-pathological Remission in Adult Patients With Eosinophilic Esophagitis
Acronym: EOS-2
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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