drugset / Trial / NCT06706427

Safety and Efficacy Study of NGGT001 in Bietti Crystalline Corneoretinal Dystrophy Subjects

NCT06706427 ↗

Phase 1/2 Active not recruiting 12 enrolled NGGT (Suzhou) Biotechnology Co., Ltd.
NaSequentialOpen-labelTreatment

Summary

The objective of this study is to evaluate the safety, tolerability, and efficacy of subretinal injection of NGGT001 in patients with Bietti Crystalline Corneoretinal Dystrophy (BCD) and to recommend the optimal dosage for future clinical administration.

Timeline

Start
2024-03-21
Primary completion
2025-11-30
Completion
2029-09-26

Drugs

EvaluationDrugModalityDoseRoute
Subject NGGT001 Gene therapy (AAV / viral vector) — Other