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.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
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
Trial Officials
Clinical Trial Management
Study Director
Regeneron Pharmaceuticals
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported