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Study identifier: NCT02735824 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Genetic Study of Immunodeficiency: Search for New Genetic Causes for Primary Immunodeficiencies

Condition: Immunologic Deficiency Syndromes · Primary Immune Deficiency (PID)  ·  Sponsor: University Children's Hospital, Zurich

PhaseN/A
Planned participants500
Who can joinAll sexes, N/A to no upper limit
Healthy volunteersYes

About this study

Individuals with suspected primary immunodeficiency will be studied and the results compared with healthy controls. Primary immunodeficiency may manifest as recurrent, severe or unusual infections as well as signs and symptoms of immune dysregulation such as autoimmunity or lymphoproliferation.

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

Talk to the study team

Jana M Pachlopnik Schmid, MD PhD  ·  +41 44 249 64 70  ·  jana.pachlopnik@kispi.uzh.ch

Always discuss trial participation with your own doctor first.

Locations (1)

Division of ImmunologyZurich, Canton of Zurich, SwitzerlandRecruiting

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Source record: clinicaltrials.gov/study/NCT02735824