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Clinical Trial Summary

This observational long-term follow-up study is designed to collect safety and efficacy data from ADA-SCID patients previously treated with autologous ex vivo gene therapy products based on the EFS-ADA LV encoding for human adenosine deaminase (ADA) gene (EFS-ADA LV), as part of the OTL-101 clinical development program. No investigational medicinal product will be administered to these patients as part of the OTL-101-6 study.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04049084
Study type Observational
Source University of California, Los Angeles
Contact
Status Enrolling by invitation
Phase
Start date September 26, 2019
Completion date August 2035

See also
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Completed NCT02022696 - 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 Phase 1
Completed NCT00008450 - Total-Body Irradiation Followed By Cyclosporine and Mycophenolate Mofetil in Treating Patients With Severe Combined Immunodeficiency Undergoing Donor Bone Marrow Transplant Phase 1