Budesonide
DrugTwice daily intake of the tablet 30 min after a meal
NCT Number: NCT06596252
The purpose of this study is to prove the non-inferiority of a 6-weeks treatment with 1 mg budesonide orodispersible tablets BID versus 2 mg budesonide orodispesible tabletss for the induction of clinico-pathological remission in adult patients with active eosinophilic esophagitis.
Interested in participating?
Request Info18 year–75 year
All sexes
Interventional
Phase 3
Department of Gastroenterology, Hospital General de Tomelloso, Tomelloso, Spain
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Twice daily intake of the tablet 30 min after a meal
Time frame: 6 weeks
Histological assessment of biopsies taken at end of treatment visit
Time frame: 6 weeks
Assessment of clinical scores assessed with questionnaires at the end of treatment visit
Contact information is provided by the study sponsor or research team.
Dr. Falk Pharma GmbH
Industry
Double-blind, Randomized, Non-inferiority Phase III Trial on the Efficacy and Tolerability of 2 mg Once Daily vs. 1 mg Twice Daily Budesonide Orodispersible Tablets in Adults With Eosinophilic Esophagitis
Acronym: EOS-4
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
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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