Overview

Safety and Efficacy of ZVS101e in Patients With Bietti 's Crystalline Dystrophy

Status:
Recruiting
Trial end date:
2028-12-01
Target enrollment:
Participant gender:
Summary
The purpose of this study was to evaluate the safety and efficacy of ZVS101e administered by subretinal injection in subjects with Bietti's crystalline dystrophy (BCD) and to select the optimal effective dose.
Phase:
Phase 1/Phase 2
Details
Lead Sponsor:
Chigenovo Co., Ltd