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Research

FARE Clinical Network

The FARE Clinical Network is a group of top food allergy centers led and coordinated by FARE (Food Allergy Research & Education). Established by FARE in 2015, the FARE Clinical Network is undergoing an expansion in 2020.  The nationwide FARE Clinical Network now encompasses 45 participating institutions that collaborate to advance the field of food allergy. By bringing top institutions together to ensure that patients with food allergies have access to state-of-the-art diagnosis and treatment, short-term and long-term care, and research that addresses factors from discovery to application, the FARE Clinical Network is setting the standard for breakthrough food allergy research and clinical care nationwide.

FCN Map

Where Is the FARE Clinical Network Site Nearest Me?

The FARE Clinical Network has expanded to encompass 45 participating institutions in 22 states and the nation’s capital.

Accelerating Advances in Food Allergy Research With the Expanded FARE Clinical Network

Driving Impact on Food Allergy Research

Food allergy centers in the FARE Clinical Network have already participated in more than 45 clinical trials in food allergy, including those that led to the development and market release of an FDA-approved treatment for peanut allergy in January 2020. Investigations at FARE Clinical Network sites continue to support the development of additional therapies, new diagnostics, and strategies for food allergy prevention and management. FARE Clinical Network sites have offered patient and community education and have helped to educate a new generation of allergists/immunologists and other care providers in best practices for food allergy prevention, diagnosis and treatment.

Doctors talking

Expanding the Access to Care and Treatments

By increasing the locations available for multi-site clinical trials, the expanded FARE Clinical Network will facilitate the development of new therapies, diagnostics and prevention strategies and will make experimental treatments more accessible to a broader number of those living with potentially life-threatening food allergies. 

Doctor with mom and kid

Your food allergy story can change the course of research and change lives.

Joining the FARE Patient Registry and making a difference is easy, convenient, and confidential.

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New Data Leads to New Breakthroughs

All institutions participating in the expanded FARE Clinical Network will contribute to the development of the data commons via the FARE Patient Registry and biobank center. Through privacy-protected data sharing, these unique resources will ultimately help researchers and clinicians understand why food allergy affects individuals differently, pointing the way to effective new treatments and diagnostics.

FARE Patient Registry

The FARE Patient Registry is a secure database of health information that allows food-allergic individuals and their caregivers to quickly, conveniently and privately share their food allergy experiences in order to help advance food allergy research.

FARE Data Commons

The FARE Data Commons will be a state-of-the-art, secure, centralized food allergy patient data platform that enables medical entities around the globe to share and access privacy-protected data in one common place and collaborate to drive research forward.

FARE Clinical Network Frequently Asked Questions