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NCT00055172

Genetic Basis of Immunodeficiency

Recruiting now Last updated 7 April 2026
What this trial tests

trial in Severe Combined Immunodeficiency in 100 participants. Currently enrolling.

Timeline
5 April 2004

Quick facts

Lead sponsorNational Heart, Lung, and Blood Institute (NHLBI)
StatusRecruiting now
Study typeOBSERVATIONAL
Enrollment100
Start date5 April 2004
Sites1 location across United States

Conditions studied

Sponsor

National Heart, Lung, and Blood Institute (NHLBI)

Who can join

Adults 6 Months to 99, any sex, with Severe Combined Immunodeficiency. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study will examine the role of hereditary factors in different forms of severe combined immunodeficiency (SCID). Patients with immunodeficiencies may be eligible for this study. Candidates include: * Patients with diminished numbers of T cells or NK cells or both, or * Patients with normal T cell and NK cell numbers but diminished T cell, B cell, or NK cell function. Relatives of patients will also be studied. Participants will have blood samples collected for genetic analysis in studies related to SCID at the National Institutes of Health and other institutions.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Severe Combined Immunodeficiency

Currently open trials in the same condition.

Other National Heart, Lung, and Blood Institute (NHLBI) trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00055172.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing