Clinical Trial

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

Not Yet Recruiting Phase 1/2
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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
Trial Details
NCT Number NCT06819514
Lead Sponsor Guangzhou Jiayin Biotech Ltd
Conditions Fabry Disease
Enrollment 16 participants
Start Date 2025-03-01
Primary Completion 2028-03-15 (estimated)
Study Completion 2028-03-15 (estimated)
Updated on ClinicalTrials.gov 2025-02-11