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Search / Trial NCT06693531

A U.S. Registry of Eosinophilic Esophagitis Adolescent and Adult Patients Treated With DUPIXENT® As Standard of Care

Launched by REGENERON PHARMACEUTICALS · Nov 14, 2024

Trial Information

Current as of June 27, 2025

Recruiting

Keywords

ClinConnect Summary

This clinical trial is looking at how well a medication called DUPIXENT® (dupilumab) works for people with eosinophilic esophagitis (EoE), a condition that affects the esophagus and can make swallowing difficult. The study is observational, meaning researchers will gather information about how patients are treated with DUPIXENT in regular care settings. By understanding the experiences of patients using this medication, the study aims to improve knowledge about EoE and help guide future treatments.

To participate, individuals must be starting DUPIXENT for EoE and able to fill out questionnaires about their symptoms and quality of life. This includes adolescents as well as adults. Participants will be asked how EoE affects their daily lives, how they feel, and whether their symptoms change during the study. The trial is currently recruiting participants, and anyone interested should check if they meet the eligibility criteria before joining.

Gender

ALL

Eligibility criteria

  • Key Inclusion Criteria:
  • 1. Initiating treatment with DUPIXENT® for EoE according to the USPI
  • 2. Able to understand and complete registry-related questionnaires (including adolescents)
  • Key Exclusion Criteria:
  • 1. Patients who have a contraindication to DUPIXENT® according to the USPI
  • 2. Treatment with DUPIXENT® within the 6 months prior to the screening assessment
  • 3. Participation in an ongoing interventional study on or within 6 months of the baseline assessment. Once enrolled in registry, participation is allowed in other ongoing studies (at the discretion of the registry investigator)
  • NOTE: Other protocol defined inclusion/exclusion criteria apply

About Regeneron Pharmaceuticals

Regeneron Pharmaceuticals, a leading biotechnology company, is dedicated to transforming the lives of patients through innovative medicines. Founded in 1988, the company specializes in the discovery, development, and commercialization of cutting-edge therapies for serious diseases, leveraging advanced genetic technologies and a robust pipeline of novel drug candidates. With a strong focus on areas such as ophthalmology, oncology, immunology, and rare diseases, Regeneron is committed to scientific excellence and collaboration, striving to deliver safe and effective treatments that address unmet medical needs and improve patient outcomes globally.

Locations

Philadelphia, Pennsylvania, United States

Charlottesville, Virginia, United States

Fort Sam Houston, Texas, United States

Durham, North Carolina, United States

Phoenix, Arizona, United States

New York, New York, United States

New Haven, Connecticut, United States

Los Angeles, California, United States

Little Rock, Arkansas, United States

Layton, Utah, United States

Orlando, Florida, United States

Littleton, Colorado, United States

Mentor, Ohio, United States

Southlake, Texas, United States

Camp Hill, Pennsylvania, United States

Flowood, Mississippi, United States

Owensboro, Kentucky, United States

Boston, Massachusetts, United States

Orange City, Florida, United States

Wichita, Kansas, United States

Rochester, New York, United States

Ocean City, New Jersey, United States

Summerville, South Carolina, United States

Atlanta, Georgia, United States

Atlanta, Georgia, United States

Sun City, Arizona, United States

Libertyville, Illinois, United States

Tacoma, Washington, United States

Chapel Hill, North Carolina, United States

Farmington, Connecticut, United States

Patients applied

0 patients applied

Trial Officials

Clinical Trial Management

Study Director

Regeneron Pharmaceuticals

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported