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Study identifier: NCT02192866 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Blood Samples for the Study of Peanut, Tree Nut and Other Food Allergies

Condition: Peanut Allergies · Tree Nut Allergies · Other Food Allergies  ·  Sponsor: University of Colorado, Denver

PhaseN/A
Planned participants270
Who can joinAll sexes, 1 Year to 75 Years
Healthy volunteersYes

About this study

Food allergies are now a major problem. These experiments involve getting blood from people with food allergies and from people without food allergies. The blood collected will be used to answer questions and find information about peanut and other food allergies. Samples will come from: * People signed up by the investigators at the University of Colorado Denver * University of North Carolina, Massachusetts General Hospital, Children's Hospital of Colorado and the Immune Tolerance Network (Benaroya Research Institute) where people have been treated for peanut allergies * University of North Carolina, Massachusetts General Hospital, National Jewish Health and The Children's Hospital in Denver where people have taken part or will take part in clinically indicated oral food challenges. Blood and health histories from the University of North Carolina, Massachusetts General Hospital, National Jewish Health, The Children's Hospital and the Immune Tolerance Network will not have personal information linked. The specific aims of this experiment are: 1. Come up with a lab test that will predict how bad an allergic reaction will be to peanuts. 2. Find out what part of a peanut causes allergic reactions. 3. Come up with preventions that can block peanut allergies. 4. Find the strongest proteins in walnuts.

This description comes directly from the study's public registry record.

Talk to the study team

Stephen Dreskin, MD, PhD  ·  303-724-7190  ·  Stephen.Dreskin@ucdenver.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University of Colorado School of MedicineDenver, Colorado, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT02192866