Clinical trial
Study of Genetic and Molecular Defects in Primary Immunodeficiency Disorders
NCT00004341 · Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), NIH · Unknown status
Key facts
| NCT number | NCT00004341 |
|---|---|
| Title | Study of Genetic and Molecular Defects in Primary Immunodeficiency Disorders |
| Lead sponsor | Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), NIH |
| Collaborators | University of Washington |
| Status | Unknown status |
| Study type | Observational |
| Conditions | X-Linked Agammaglobulinemia, X-Linked Hyper IgM Syndrome, Wiskott-Aldrich Syndrome, Leukocyte Adhesion Deficiency Syndrome |
| Start date | Jul 1, 1995 |
| First posted | Oct 19, 1999 |
| Last update posted | Jun 24, 2005 |
| Countries | United States |
At a glance
- 1–9 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: