Once Daily Versus Twice Daily Budesonide Orodispersible Tablets for Induction of Remission in EoE

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18-75
SponsorDr. Falk Pharma GmbH

About this trial

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.

Eligibility criteria

Qualifiers

Signed informed consent,

Male or female patients, 18 to 75 years of age,

Confirmed clinico-pathological diagnosis of eosinophilic esophagitis (EoE) according to established diagnostic criteria

Active symptomatic and histological EoE

Disqualifiers

Clinical and endoscopic signs of gastroesophageal reflux disease (GERD),

Achalasia, scleroderma esophagus, or systemic sclerosis,

Other clinically evident causes than EoE for esophageal eosinophilia,

Any concomitant esophageal disease and relevant gastro-intestinal disease (celiac disease, inflammatory bowel disease, oropharyngeal or esophageal bacterial, viral, or fungal infection [candida esophagitis]),

Trial design

Treatments tested in this trial

  • Budesonide

Treatment groups

308 Participants
are divided into 3 treatment groups

Locations

26
Spain
Department of Gastroenterology, Hospital General de Tomelloso13700, Tomelloso Spain
United States
Arizona
Dr. Falk Investigational Site85259, Scottsdale United States
Arkansas
Dr. Falk Investigational Site72205, Little Rock United States
California
Dr. Falk Investigational Site92037, La Jolla United States

Sponsors and collaborators

Dr. Falk Pharma GmbH

Lead sponsor