This observational research study is to better understand patients with eosinophilic esophagitis (EoE) who have recently been prescribed DUPIXENT® (dupilumab). The purpose of this research study is to look at how DUPIXENT is used in normal care of patients with EoE. Possible benefits to others include a better understanding of EoE and helping to inform research and clinical trial design leading to treatment decisions in this patient population going forward. Patient questionnaires will measure the following: * How EoE makes one feel * EoE signs and/or symptoms, eg, how difficult it is to swallow * How EoE affects quality-of-life * How EoE impacts aspects of daily life * How EoE symptoms have changed throughout the study
Study Type
OBSERVATIONAL
Enrollment
368
No investigational agents will be provided. Dupilumab will be prescribed as per usual clinical practice and will not be provided by the sponsor.
Phoenix Childrens Hospital
Phoenix, Arizona, United States
Arizona Digestive Health/GI Alliance
Sun City, Arizona, United States
Arkansas Childrens Hospital
Little Rock, Arkansas, United States
Scripps Clinic
La Jolla, California, United States
University of California Los Angeles (UCLA)
Los Angeles, California, United States
Demographic characteristic of participants who receive dupilumab for EoE: Age
Time frame: Baseline and up to 3 years after treatment initiation
Demographic characteristic of participants who receive dupilumab for EoE: Race
Time frame: Baseline and up to 3 years after treatment initiation
Demographic characteristic of participants who receive dupilumab for EoE: Weight
Time frame: Baseline and up to 3 years after treatment initiation
Demographic characteristic of participants who receive dupilumab for EoE: Height
Time frame: Baseline and up to 3 years after treatment initiation
Disease characteristics of participants who receive dupilumab for EoE: Esophagogastroduodenoscopy (EGD)
Time frame: Baseline and up to 3 years after treatment initiation
Disease characteristics of participants who receive dupilumab for EoE: Dilation/impaction history
Time frame: Baseline and up to 3 years after treatment initiation
Disease characteristics of participants who receive dupilumab for EoE: Dietary interventions
Time frame: Baseline and up to 3 years after treatment initiation
Disease characteristics of participants who receive dupilumab for EoE: Medical history
Time frame: Baseline and up to 3 years after treatment initiation
EoE medication history of participant
Time frame: Previous 1 year and up to 3 years after treatment initiation
Non-EoE medication history of participant
Time frame: Previous 3 months and up to 3 years after treatment initiation
Prior dupilumab exposure history of participant
Time frame: Baseline and up to 3 years after treatment initiation
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
University of Southern California Keck School of Medicine
Los Angeles, California, United States
University of California, San Francisco
Oakland, California, United States
Stanford University
Palo Alto, California, United States
University of California San Francisco (UCSF)
San Francisco, California, United States
Childrens Hospital Colorado
Aurora, Colorado, United States
...and 44 more locations