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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Investigation of Filaggrin Gene Mutations Among Latinx Patients With Atopic DermatitisCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Hypersensitivity, Immediate, Skin Diseases, Eczematous, Skin and Connective Tissue Diseases, atopic eczema, dermatitis, hereditary disease, hereditary skin disorder, immune system disorder, skin disorderEnrolling by invitationNot stated2026-04-24NCT06464133