drugset / Trial / NCT05071222

Safety and Efficacy Study of Transplantation of Autologous CD34+ Cells Transduced With the G2ARTE Lentiviral Vector Expressing the DCLRE1C cDNA in Artemis (DCLRE1C) Deficient Severe Combined Immunodeficiency Patients (ARTEGENE)

NCT05071222 ↗

NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the Safety and Efficacy of Gene Therapy of the severe combined immunodeficiency (SCID) caused by mutations in the human DCLRE1C gene (Artemis) by transplantation of a single dose of autologous CD34+ cells transduced ex vivo with the G2ARTE lentiviral vector expressing the DCLRE1C cDNA.

Timeline

Start
2023-07-19
Primary completion
2041-11-19
Completion
2041-11-19

Drugs

EvaluationDrugModalityDoseRoute
Subject ARTEGENE Unknown — Intravenous