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Adenosine Deaminase Deficiency - 18 Studies Found

Status Study
Completed Study Name: Gene Therapy ADA Deficiency
Condition: Adenosine Deaminase Deficiency
Date: 2011-01-18
Interventions: Biological: Intravenous infusion of transduced cells Intravenous infusion of transduced cells
Completed Study Name: Treatment of SCID Due to ADA Deficiency With Autologous Transplantation of Cord Blood or Hematopoietic CD 34+ Cells After Addition of a Normal Human ADA cDNA by the EFS-ADA Lentiviral Vector
Condition:
  • Adenosine Deaminase Deficiency
  • ADA-SCID Date: 2013-12-20
    Interventions: Genetic: Lentiviral Gene Transfer
Withdrawn Study Name: Quality of Life and Neuropsychiatric Sequelae in Patients Treated With Gene Therapy for ADA-SCID and in Their Parents
Condition: ADA-SCID
Date: 2010-08-14
Completed Study Name: Autologous Cryopreserved CD34+ Hematopoietic Cells Transduced With EFS-ADA Lentivirus for ADA SCID
Condition: Severe Combined Immunodeficiency Due to ADA Deficiency
Date: 2016-12-19
Interventions: Biological: Infusion of autologous cryopreserved EFS-ADA LV CD34+ cells Infusion of OTL-101 after reduce
Completed Study Name: EZN-2279 in Patients With ADA-SCID
Condition:
  • ADA-SCID
  • Adenosine Deaminase Deficiency Date: 2011-08-18
    Interventions:
    • Biological: EZN-2279 weekly ad
Completed Study Name: Lentiviral Gene Therapy for Adenosine Deaminase (ADA) Deficiency
Condition:
  • Adenosine Deaminase Deficiency
  • Severe Combined Immunodeficienci
    Date: 2011-06-23
    Interventions: Genetic: EF1αS-ADA lentiviral vector transduced patient Cd34+ cells EF1αS-ADA lentiviral vecto
Active, not recruiting Study Name: Autologous Transplant of EFS-ADA Modified Bone Marrow Cells for ADA-Deficient Severe Combined Immunodeficiency (SCID)
Condition: ADA-SCID
Date: 2013-05-07
Interventions: Genetic: EFS-ADA transduced CD34+ cells from the bone marrow Eligible subjects will undergo bone marrow
Completed Study Name: Gene Therapy for ADA-SCID
Condition: Severe Combined Immunodeficiency Syndrome
Date: 2008-01-08
Interventions: Genetic: gene transduced PBL and/or gene transduced HSC infusions of autologous PBL and/or HSC transduce
Active, not recruiting Study Name: ADA Gene Transfer Into Hematopoietic Stem/Progenitor Cells for the Treatment of ADA-SCID
Condition: Immunologic Deficiency Syndromes
Date: 2008-01-10
Interventions: Genetic: Gene transduced CD34+ cells infusion of autologous CD34+ cells transduced with retroviral vecto
Completed Study Name: Participation in a Research Registry for Immune Disorders
Condition:
  • ADA-SCID
  • Adenosine Deaminase Deficiency Date: 2013-09-25
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