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Active, not recruitingPhase 3

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

Key facts

Who runs it
Dr. Falk Pharma GmbH
Where
Ann Arbor, Boise, Boston, Chapel Hill, Cleveland, Doral, Freehold, Harlingen, La Jolla, Little Rock, Lynchburg, Mentor, New Port Richey, New York, Philadelphia, Rochester, Salt Lake City, San Diego, Scottsdale, and Wyoming, United StatesSee the 20 sitesAlso in 4 other countries, 23 sites
Status
Active, not recruiting
Phase
Phase 3
People taking part
308 people, planned
Started
21 May 2021
Expected to end
Mar 2028
Type of study
Interventional, 3 groupsOne group gets an existing treatment, for comparison.
Treatments tested
  • Budesonide
Record updated
28 August 2026

Who can take part

Age
18 years to 75 years
Sex
Women and men
Healthy volunteers
Cannot take part

The registry criteria, word for word

Show all 16 criteriaShow less

Who can take part

  • 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
  • Negative pregnancy test in females of childbearing potential at baseline visit

Who cannot take part

  • Any concomitant esophageal disease and relevant gastro-intestinal disease (celiac disease, inflammatory bowel disease, oropharyngeal or esophageal bacterial, viral, or fungal infection [candida esophagitis]),
  • History of esophageal surgery at any time or of esophageal dilation procedures within the last 4 weeks prior to screening visit, or need for an immediate endoscopic intervention due to a stricture
  • Upper gastrointestinal bleeding within 8 weeks prior to baseline visit,
  • Clinical and endoscopic signs of gastroesophageal reflux disease (GERD),
  • Any relevant systemic disease (e.g., AIDS, active tuberculosis, hepatitis B or C),
  • If careful medical monitoring is not ensured: cardiovascular disease, diabetes mellitus, osteoporosis, active peptic ulcer disease, glaucoma, cataract, or infection,
  • Liver cirrhosis or portal hypertension,
  • History of cancer in the last five years,
  • Achalasia, scleroderma esophagus, or systemic sclerosis,
  • Other clinically evident causes than EoE for esophageal eosinophilia,
  • Existing or intended pregnancy or breast-feeding

Where in United States

Also in 4 other countries, 23 sites

  • WyomingAnn Arbor, United States
  • Dr. Falk Investigational SiteBoise, United States
  • Dr. Falk Investigational SiteBoston, United States
  • Dr. Falk Investigational SiteChapel Hill, United States
  • Dr Falk Investigational SiteCleveland, United States
  • Dr Falk Investigational SiteDoral, United States
  • Dr. Falk Investigational SiteFreehold, United States
  • Dr Falk Investigational SiteHarlingen, United States
  • Dr. Falk Investigational SiteLa Jolla, United States
  • Dr. Falk Investigational SiteLittle Rock, United States
  • Dr. Falk Investigational SiteLynchburg, United States
  • Dr. Falk Investigational SiteMentor, United States
  • Dr. Falk Investigational SiteNew Port Richey, United States
  • Dr Falk Investigational SiteNew York, United States
  • WyomingPhiladelphia, United States
  • Dr. Falk Investigational SiteRochester, United States
  • Dr. Falk Investigational SiteSalt Lake City, United States
  • Dr. Falk Investigational SiteSan Diego, United States
  • Dr. Falk Investigational SiteScottsdale, United States
  • Dr. Falk Investigational SiteWyoming, United States

About the trial

What the trial wants to find out

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.

The 3 groups in the trial

  • Arm ATreatment being tested

    Budesonide 2 mg orodispersible tablet once daily

    Treatment: Budesonide

  • Arm BExisting treatment, for comparison

    Budesonide 1 mg orodispersible tablet twice daily

    Treatment: Budesonide

  • OLETreatment being tested

    Open label extension with Budesonide 0.5 mg or 1 mg orodispersible tablet twice daily

    Treatment: Budesonide

Data and sources

Registry record
Listed on ClinicalTrials.gov and on the EU's official list of trials (CTIS).
Official title
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
Record updated
28 August 2026