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.

Want to learn more about this trial?

Request More Info

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: April 14, 2026