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Clinical Trials on X-linked Severe Combined Immunodeficiency

Total 21 results

    • NCT01410019
      Unknown status
      Gene Therapy for X-linked Severe Combined Immunodeficiency
      Conditions: X-linked Severe Combined Immunodeficiency
    • NCT01175239
      Unknown status
      Gene Therapy for X-linked Severe Combined Immunodeficiency (SCID-X1)
      Conditions: X-linked Severe Combined Immunodeficiency
    • NCT03315078
      Recruiting
      Lentiviral Gene Transfer for Treatment of Children Older Than 2 Years of Age With X-Linked Severe Combined Immunodeficiency
      Conditions: X-Linked Combined Immunodeficiency Diseases
    • NCT01306019
      Recruiting
      Lentiviral Gene Transfer for Treatment of Children Older Than Two Years of Age With X-Linked Severe Combined Immunodeficiency (XSCID)
      Conditions: X-Linked Severe Combined Immune Deficiency (XSCID)
    • NCT00490100
      Terminated
      Treatment for Growth Failure in Patients With X-Linked Severe Combined Immunodeficiency: Phase 2 Study of Insulin-Like Growth Factor-1
      Conditions: Growth Failure; X-linked Severe Combined Immunodeficiency (XSCID); Growth Hormone Resistence
    • NCT03601286
      Recruiting
      Lentiviral Gene Therapy for X-linked Severe Combined Immunodeficiency
      Conditions: Severe Combined Immunodeficiency, X-Linked
    • NCT04286815
      Recruiting
      Gene Therapy for X Linked Severe Combined Immunodeficiency
      Conditions: Gene Therapy
    • NCT01512888
      Recruiting
      Gene Transfer for X-Linked Severe Combined Immunodeficiency in Newly Diagnosed Infants
      Conditions: Severe Combined Immunodeficiency Disease, X-linked
    • NCT03217617
      Recruiting
      Gene Transfer for SCID-X1 Using a Self-inactivating Lentiviral Vector （TYF-IL-2Rg）
      Conditions: SCID, X Linked
    • NCT00028236
      Completed
      Stem Cell Gene Therapy to Treat X-Linked Severe Combined Immunodeficiency (XSCID)
      Conditions: Severe Combined Immunodeficiency
    • NCT02915406
      No longer available
      cliniMACs HUD for T Cell Depletion
      Conditions: x Linked Combined Immunodeficiency
    • NCT00006335
      Completed
      Influences on Female Adolescents' Decisions Regarding Testing for Carrier Status of XSCID
      Conditions: Severe Combined Immunodeficiency
    • NCT03311503
      Recruiting
      Phase I/II Trial of Lentiviral Gene Transfer for SCID-X1 With Low Dose Targeted Busulfan Conditioning
      Conditions: Severe Combined Immunodeficiency, X Linked; Gene Therapy
    • NCT01129544
      Active, not recruiting
      Gene Transfer for Severe Combined Immunodeficiency, X-linked (SCID-X1) Using a Self-inactivating (SIN) Gammaretroviral Vector
      Conditions: Severe Combined Immunodeficiency
    • NCT00008450
      Completed
      Total-Body Irradiation Followed By Cyclosporine and Mycophenolate Mofetil in Treating Patients With Severe Combined Immunodeficiency Undergoing Donor Bone Marrow Transplant
      Conditions: Adenosine Deaminase Deficiency; Autosomal Recessive Disorder; Immune System Disorder; Purine-Nucleoside Phosphorylase Deficiency; Severe Combined Immunodeficiency; Severe Combined Immunodeficiency With Absence of T and B Cells; X-Linked Severe Combined Immunodeficiency
    • NCT00128973
      Recruiting
      Evaluation of Patients With Immune Function Abnormalities
      Conditions: Chronic Granulomatous Disease (CGD); X-Linked Severe Combined Immune Deficiency (XSCID); Leukocyte Adhesion Deficiency 1 (LAD); Graft Versus Host Disease (cGvHD)
    • NCT01346150
      Enrolling by invitation
      Patients Treated for SCID (1968-Present)
      Conditions: SCID; ADA-SCID; XSCID; Leaky SCID; Omenn Syndrome; Reticular Dysgenesis
    • NCT01186913
      Enrolling by invitation
      Natural History Study of SCID Disorders
      Conditions: Severe Combined Immunodeficiency (SCID); Leaky SCID; Omenn Syndrome; Reticular Dysgenesis; ADA SCID; XSCID
    • NCT00006319
      Active, not recruiting
      Molecular and Clinical Studies of Primary Immunodeficiency Diseases
      Conditions: Wiskott- Aldrich Syndrome; ADA Deficient SCID
    • NCT00006054
      Terminated
      Allogeneic Bone Marrow Transplantation in Patients With Primary Immunodeficiencies
      Conditions: Immunologic Deficiency Syndromes; Chediak-Higashi Syndrome; Common Variable Immunodeficiency; Graft Versus Host Disease; X-Linked Lymphoproliferative Syndrome; Familial Erythrophagocytic Lymphohistiocytosis; Hemophagocytic Lymphohistiocytosis; X-linked Agammaglobulinemia; Wiskott-Aldrich Syndrome; Chronic Granulomatous Disease; X-linked Hyper IgM Syndrome; Severe Combined Immunodeficiency; Leukocyte Adhesion Deficiency Syndrome; Virus-Associated Hemophagocytic Syndrome
    • NCT01821781
      Recruiting
      Immune Disorder HSCT Protocol
      Conditions: Immune Deficiency Disorders; Severe Combined Immunodeficiency; Chronic Granulomatous Disease; X-linked Agammaglobulinemia; Wiskott-Aldrich Syndrome; Hyper-IgM; DiGeorge Syndrome; Chediak-Higashi Syndrome; Common Variable Immune Deficiency; Immune Dysregulatory Disorders; Hemophagocytic Lymphohistiocytosis; IPEX; Autoimmune Lymphoproliferative Syndrome; X-linked Lymphoproliferative Syndrome
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