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RECRUITING
NCT06705387
PHASE2

Dupilumab Versus Topical Corticosteroid Effectiveness - Comparison in the Treatment of Stenotic EoE

Sponsor: University of Colorado, Denver

View on ClinicalTrials.gov

Summary

The goal of this clinical trial is to \[primary purpose: e.g., learn if intervention or health behavior can treat, prevent, diagnose etc.\] in \[describe participant population/primary condition; could include any of the following: sex/gender, age groups, healthy volunteers\]. The main question\[s\] it aims to answer \[is/are\]: Does dupilumab or swallowed topical fluticasone improve the diameter of the esophagus more? Does dupilumab or swallowed topical fluticasone reduce inflammation in the esophagus more? Are comparative effective clinical trials feasible in this patient population? Researchers will compare dupilumab 300 mg weekly compared to swallowed fluticasone to see if there is a difference in treatment response. Participants will be asked to: * Be randomized to either dupilumab sq weekly or swallowed topical fluticasone twice daily. * Participate in 8 study visits over 52 weeks * Complete questionnaires * Have an endoscopy with biopsies and EndoFLIP measurements. * Swallow an Esophageal String Test

Official title: DeTECTS: Dupilumab Versus Topical Corticosteroid Effectiveness - Comparison in the Treatment of Stenotic EoE

Key Details

Gender

All

Age Range

12 Years - 25 Years

Study Type

INTERVENTIONAL

Enrollment

72

Start Date

2024-12-23

Completion Date

2027-03

Last Updated

2025-03-14

Healthy Volunteers

No

Interventions

BIOLOGICAL

Dupilumab

Subcutaneous injection of 300mg per week for 16 weeks.

DRUG

Fluticasone

Metered dose swallowed topical corticosteroid, given 1760mcg per day for 16 weeks.

Locations (1)

Children's Hospital Colorado/University of Colorado School of Medicine

Aurora, Colorado, United States