Status: Recruiting
A Registry for the Food Allergy Community
The FARE Patient Registry will serve as a prospective, observational food allergy reporting system that stores detailed health and other basic information about patients' real-world experiences with food allergies, to encourage open sharing of de-identified data and participation in clinical trials. The FARE Patient Registry intends to make and support scientific discoveries by enabling the food allergy community to participate directly in research.
Participants needed: 23,000
Trial details
Biological sex: AllType: ObservationalSponsor: Food Allergy Research & EducationUpdated: Mar 12, 2025Locations: 1Duration: 5 Years
Eligibility criteria
Individuals with diagnosed food allergy
Individuals without food allergy