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RECRUITING
NCT03311503
PHASE1/PHASE2

Phase I/II Trial of Lentiviral Gene Transfer for SCID-X1 With Low Dose Targeted Busulfan Conditioning

Sponsor: David Williams

View on ClinicalTrials.gov

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

BIOLOGICAL

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