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Phase I/II Trial of Lentiviral Gene Transfer for SCID-X1 With Low Dose Targeted Busulfan Conditioning
Sponsor: David Williams
Summary
This is a phase I/II open label multi-center study in which patients will receive low dose targeted busulfan followed by infusion of autologous CD34+ selected bone marrow or mobilized peripheral blood cells transduced with the G2SCID vector. Subjects will be enrolled over 3 years and be followed for 2 years post-infusion on this protocol, then followed long-term on a separate long-term follow-up protocol. Enrollment of subjects will be agreed upon by representatives of both sites. Data will be collected uniformly from both sites through an electronic capture system and key laboratory studies will be centralized. Harvest, cellular manufacturing and infusion will occur at each site using the same SOPs. Key aspects of cellular product characterization will be centralized
Key Details
Gender
MALE
Age Range
0 Years - 5 Years
Study Type
INTERVENTIONAL
Enrollment
12
Start Date
2018-02-26
Completion Date
2028-01-01
Last Updated
2025-12-11
Healthy Volunteers
No
Interventions
autologous CD34+ cell transduced with G2SCID vector
single infusion of autologous CD34+ cells transduced with the self-inactivating (SIN) lentiviral vector G2SCID
Locations (4)
Mattel Children's Hospital - UCLA
Los Angeles, California, United States
Emory University/Childrens Healthcare of Atlanta
Atlanta, Georgia, United States
Boston Childrens Hospital
Boston, Massachusetts, United States
Cincinnati Children's Hospital Medical Center
Cincinnati, Ohio, United States