Frontlight ResearchEarly access
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