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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Study of Chediak-Higashi SyndromeChediak-Higashi syndrome, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Hemic and Lymphatic Diseases, Infections, Nutritional and Metabolic Diseases, Primary Immunodeficiency Diseases, Skin and Connective Tissue Diseases, albinism, blood coagulation disease, blood platelet disease, eye disorder, hematologic disorder, hemorrhagic disease, hereditary disease, hereditary skin disorder, hypopigmentation of the skin, immune system disorder, inborn disorder of amino acid metabolism, inborn error of immunity, inborn errors of metabolism, leukocyte disorder, metabolic disease, phagocyte bactericidal dysfunction, platelet storage pool deficiency, skin disorder, skin pigmentation disorderRecruitingNot stated2026-08-28NCT00005917

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Research sitesCityCountryLinked trials
National Institutes of Health Clinical CenterBethesdaUnited States800