drugset / Trial / NCT05858983

Gene Therapy in Subjects With Biallelic RPE65 Mutation-associated Retinal Dystrophy

NCT05858983 ↗

Phase 1/2 Recruiting 9 enrolled Frontera Therapeutics
Non-randomizedSequentialOpen-labelTreatment

Summary

The goal of this clinical trial is to evaluate the safety, tolerability and efficacy of subretinal administration of FT-001 in subjects with biallelic RPE65 mutation-associated retinal dystrophy.

Timeline

Start
2022-11-30
Primary completion
2025-11-30
Completion
2029-11-30

Drugs

EvaluationDrugModalityDoseRoute
Subject FT-001 Unknown — Other