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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Long Term Safety Follow up of Haematopoietic Stem Cell Gene Therapy for the Wiskott Aldrich SyndromeCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Cytopenia, Hemic and Lymphatic Diseases, Primary Immunodeficiency Diseases, Wiskott-Aldrich syndrome, X-linked disease, blood coagulation disease, hematologic disorder, hemorrhagic disease, hereditary disease, immune system disorder, inborn error of immunity, inherited blood coagulation disorder, leukocyte disorder, leukopenia, lymphopeniaActive, not recruitingPhase 1 / Phase 22021-06-03NCT02333760

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OrganizationsLinked trials
Genethon6

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Research sitesCityCountryLinked trials
Hopital Necker - Enfants MaladesParisFrance1
UCL Institute of Child HealthLondonUnited Kingdom1