drugset / Trial / NCT06539624

Evaluate the Safety and Preliminary Efficacy of EXG110 in Subjects With Fabry Disease

NCT06539624 ↗

Non-randomizedSequentialOpen-labelTreatment

Summary

Objective: To explore the safety and tolerability of different doses of EXG110 with Fabre disease

Timeline

Start
2024-10-16
Primary completion
2027-04-09
Completion
2027-04-09

Drugs

EvaluationDrugModalityDoseRoute
Subject EXG110 Gene therapy (AAV / viral vector) — Intravenous

Indications