Study of Genetic and Molecular Defects in Primary Immunodeficiency Disorders

Status unconfirmed

Conditions studied: X-Linked Agammaglobulinemia, X-Linked Hyper IgM Syndrome, Wiskott-Aldrich Syndrome, Leukocyte Adhesion Deficiency Syndrome

In brief

OBJECTIVES: I. Identify the molecular defects responsible for primary immunodeficiency disorders. II. Explore the mutations within each syndrome to better understand the genetics of these disorders. III. Study the function of the Wiskott-Aldrich syndrome proteins (WASP). IV. Design methods to identify carriers and for prenatal diagnosis. V. Explore new avenues for therapy.

Key facts

Study ID

NCT00004341

Run by

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Starts

1995-07-01

Last updated by the study team

2005-06-24

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

Where it is running

• University of Washington School of Medicine — Seattle, Washington, United States

Full record on ClinicalTrials.gov

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