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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
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

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record

Print a page for my doctor

Data 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