NCT03351829

Gene Therapy of Beta Thalassemia Using a Self-inactivating Lentiviral Vector

Study Summary

This is a Phase I/II clinical trial of gene transfer for treating Beta-thalassemia using a self-inactivating lentiviral vector to functionally correct the defective gene(s). The objectives are to evaluate the safety and efficacy of the gene transfer clinical protocol.

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Interventions

Gene-modified autologous stem cellsGENETIC
1 infusion for 5x10\^6\~1x10\^7 gene-modified cells; or more infusions depending on the circumstances

Study Locations

FacilityCityStateCountry
Shenzhen Geno-immune Medical InstituteShenzhenGuangdongChina

Official Trial Information

View on ClinicalTrials.gov

Data sourced from ClinicalTrials.gov. Last updated: April 14, 2026