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.
Individuals with diagnosed food allergy
Individuals without food allergy
The population includes males and females of all ages with one or more food allergy or those who are at risk of food-induced anaphylaxis.
Cohort
Prospective
Not listed
Create a registry to characterize the extent of food allergy, its etiology and other factors that contribute to disease development.
Click on the lead sponsor to view all of their trials.
