drugset / Trial / NCT06819514

The Safety and Efficacy of Intravenous EXG110 in Patients With Fabry Disease

NCT06819514 ↗

Phase 1/2 Not yet recruiting 16 enrolled Guangzhou Jiayin Biotech Ltd
Non-randomizedSequentialOpen-labelTreatment

Summary

A phase 1/2, multicenter, open-label, Dose-escalation study to evaluate the safety and efficacy of intravenous EXG110 in patients with Fabry disease

Timeline

Start
2025-03-01
Primary completion
2028-03-15
Completion
2028-03-15

Drugs

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

Indications