Regeneron Dupixent Registry Eosinophilic Esophagitis EoE

Purpose of this Study

We are doing this study to learn more about the long-term effectiveness of an approved medicine that is prescribed for the treatment of EoE. We want to know how will dupilumab (Dupixent®) works over time when EoE patients and their doctors choose it as therapy. Dupilumab was approved by the FDA in May 2022 to treat EoE and was the first drug approved for this purpose.

Who Can Participate?

Eligibility

Adults ages 18+ who plan to start using dupilumab as a long-term therapy for EoE. For more information, contact the study team at nicole.pavlus@duke.edu.

Age Range

18-110

Sex/Genders

Male (cisgender)
Female (cisgender)
Non-binary or gender fluid
Transgender male
Transgender female
Looking for Healthy Participants
No

What is Involved?

Description

If you choose to join this study, you will give us permission to collect information from your routine doctor visits to manage your EoE. Additionally, you will have research "check-ins" with the study team approximately every 3 months for the first 6 months, and then every 6 months thereafter to answer questionnaires. You will be in the study for up to 3 years (36 months).

Locations

Duke University Hospital

Visit Timing

Weekdays

Compensation

Yes

Spanish Materials Available

No

Study Details

Full Title

A U.S. Registry of Eosinophilic Esophagitis Patients Treated with Dupixent As Standard of Care

Principal Investigator

David
Leiman

Protocol Number

PRO00117064

NCT ID

NCT06693531

Phase

N/A

Enrollment Status

Pending Open to Enrollment