NCT03217032

Lentiviral FVIII Gene Therapy for Hemophilia A

Study Summary

This study is a Phase I trial using an advanced lentiviral vector to deliver a functional gene for human clotting factor VIII into patients with hemophilia A, to evaluate the safety and efficacy of infusion of lentiviral gene modified autologous stem cells in patients.

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Interventions

YUVA-GT-F801BIOLOGICAL
Lentiviral factor VIII gene modified autologous hematopoeitic stem cells and mesenchymal stem cells

Study Locations

FacilityCityStateCountry
Shenzhen Geno-immune Medical InstituteShenzhenGuangdongChina

Official Trial Information

View on ClinicalTrials.gov

Data sourced from ClinicalTrials.gov. Last updated: May 29, 2026