Recruiting
Phase 3

Dupilumab

Sponsor:

Regeneron Pharmaceuticals

Code:

NCT07112378

Conditions

Eosinophilic Esophagitis (EoE)

Eligibility Criteria

Sex: All

Age: 0 - 6

Healthy Volunteers: Not accepted

Interventions

dupilumab

Study Details

Brief summary:

This study is researching an experimental drug called dupilumab (called "study drug"). The study is focused on children with active eosinophilic esophagitis (EoE; an inflammatory disease of the esophagus) which impacts feeding and nourishment.

The aim of the study is to see how safe, tolerable, and effective the study drug is when given for 24 weeks to children with active EoE.

The study is looking at several other research questions, including:

  • What side effects may happen from taking the study drug
  • How much study drug is in the blood at different times
  • Whether the body makes antibodies against the study drug (which could make the drug less effective or could lead to side effects)

Conditions

Eosinophilic Esophagitis (EoE)

Study ID

NCT07112378

Start date

Nov 10, 2025

Status verified date

Aug, 2026

Completion date

Oct 9, 2028

Anticipated

Primary completion date

Jun 19, 2028

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 0 - 6

Healthy Volunteers: Not accepted

Key Inclusion Criteria:

1. Pediatric patients aged ≥6 months and weighing ≥5 kg and <15 kg at screening with active EoE
2. History of symptom(s) determined by the investigator to be the result of EoE in the month prior to screening, as defined in the protocol
3. Baseline endoscopic biopsies, performed during the screening period, with a demonstration on central reading of intraepithelial eosinophilic infiltration in at least 2 of the 3 biopsied esophageal regions, as defined in the protocol

Key Exclusion Criteria:

1. Prior participation in a dupilumab clinical trial or past or current treatment with dupilumab
2. 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
3. Other causes of esophageal eosinophilia or the following conditions: eosinophilic gastroenteritis, hypereosinophilic syndrome, and eosinophilic granulomatosis with polyangiitis (Churg-Strauss syndrome)
4. Active Helicobacter pylori infection
5. History of Crohn's disease, ulcerative colitis, celiac disease, or prior esophageal surgery
6. Any esophageal stricture unable to be passed with a standard, diagnostic, upper endoscope or any critical esophageal stricture that requires dilation at screening
7. History of bleeding disorders or esophageal varices that, in the opinion of the investigator, would put the patient at undue risk for significant complications from an endoscopic procedure
8. Treatment with swallowed topical corticosteroids within 8 weeks prior to baseline standard of care endoscopy

NOTE: Other Protocol-Defined Inclusion/Exclusion Criteria Apply

Study Design

Enrollment

20 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Dosing Regimen 1

experimental: Dosing Regimen 2

Interventions

dupilumab

Administered as defined in the protocol

Primary outcome measure

  • Incidence of treatment-emergent Serious Adverse Events (SAEs) [ Time Frame: Up to 24 Weeks ]

Central Contacts and Locations

Central contacts

Clinical Trials Administrator

844-734-6643clinicaltrials@regeneron.com

Locations

Phoenix Childrens Hospital

Recruiting

Phoenix, Arizona, United States, 85016

University of California San Francisco (UCSF)

Recruiting

San Francisco, California, United States, 94143

Children's Hospital Colorado

Recruiting

Aurora, Colorado, United States, 80045

GI Care for Kids LLC

Recruiting

Atlanta, Georgia, United States, 30342

Massachusetts General Hospital

Recruiting

Boston, Massachusetts, United States, 02114

Weill Cornell Medicine

Recruiting

New York, New York, United States, 10065

University of North Carolina, Bioinformatics Building

Recruiting

Chapel Hill, North Carolina, United States, 27599

Children's Hospital of Philadelphia

Recruiting

Philadelphia, Pennsylvania, United States, 19104

Medical University of South Carolina

Recruiting

Charleston, South Carolina, United States, 29425

Cook Children's Medical Center

Recruiting

Fort Worth, Texas, United States, 76104

University of Virginia

Recruiting

Charlottesville, Virginia, United States, 22908

Seattle Children's Hospital

Recruiting

Seattle, Washington, United States, 98105

Medical College of Wisconsin, Children's Hospital of Wisconsin

Recruiting

Milwaukee, Wisconsin, United States, 53226

More Information

Sponsor

Regeneron Pharmaceuticals

Last update posted

Aug 20, 2026

Last verified

Aug, 2026

Keywords

  • Type 2 Inflammatory
  • Allergic/immune-mediated
  • Esophageal dysfunction

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-08. This information was provided to ClinicalTrials.gov by Regeneron Pharmaceuticals on 2026-08-20.