Frontlight ResearchEarly access
Taking peoplePhase 4
Optimization of Dupilumab Maintenance Dosing in Eosinophilic Esophagitis
Key facts
- Who runs it
- Amsterdam UMC Stichting
- Where
- Netherlands1 site in 1 countryChoose a country to see its sites
- Trial code
- Status
- Recruiting
- Phase
- Phase 4
- People taking part
- 160 people, planned
- Started
- 12 Nov 2026
- Expected to end
- 1 Jul 2029
- Type of study
- Interventional
- Record updated
- 3 November 2026
Who can take part
- Age
- 18 years and older
- Sex
- Women and men
- Healthy volunteers
- Cannot take part
The registry criteria, word for word
Show all 11 criteriaShow less
Who can take part
- Male or female ≥18 years of age
- Documented diagnosis of EoE by endoscopic biopsy, confirmed by intraepithelial eosinophilic infiltration (peak cell count ≥15 eosinophils [eos]/high-power field [hpf])
- On dupilumab therapy for a minimum of 24 weeks prior to screening
- Documented complete remission consisting of clinical (DSQ <10), endoscopic (EREFS score ≤2), and histologic remission (PEC <15 eos/hpf), confirmed at screening
Who cannot take part
- Treatment with swallowed topical or systemic corticosteroids within 8 weeks prior to baseline
- Initiation of PPI therapy or any change in PPI dose within the 8 weeks prior to screening. Patients receiving PPIs must remain on same dose throughout the study
- Initiation or change of a food-elimination diet regimen or re-introduction of a previously eliminated food group in the 6 weeks prior to screening. Patients on a food-elimination diet must remain on the same diet throughout the study
- Oesophageal dilatation within the 12 weeks prior to screening
- Any contraindication or safety condition that would preclude the standard, approved use of dupilumab
- Presence of an esophageal stricture that cannot be traversed with a standard, diagnostic, 9 to 10 mm upper endoscope or any critical oesophageal stricture that requires dilation at screening
- Pregnant or breastfeeding women, or women planning to become pregnant or breastfeed during the study
This trial has no sites in United States.
It has sites in one country. Choose a country to see its sites.
About the trial
What the trial wants to find out
To determine whether dose de-escalation of dupilumab 300mg SC Q2W is non-inferior to 300mg SC QW dosing in maintaining complete remission, a composite endpoint of clinical, endoscopic, and histologic remission in adults with eosinophilic esophagitis.
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record
Print a page for my doctorData and sources
- Registry record
- Listed on the EU's official list of trials (CTIS).
- Official title
- Optimization of Dupilumab Maintenance Dosing in Eosinophilic Esophagitis: A Phase IV, Randomized, Controlled, Single-Blind, Non-Inferiority Study
- Record updated
- 3 November 2026