Overview
A Follow-up Study to Evaluate the Safety of RetinoStat® in Patients With Age-Related Macular Degeneration
Status:
Active, not recruiting
Active, not recruiting
Trial end date:
2029-03-01
2029-03-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
The purpose of this study is to examine the long term safety of an experimental gene transfer agent, RetinoStat®, designed to treat neovascular age-related macular degeneration.Phase:
Phase 1Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Oxford BioMedica
Criteria
Inclusion Criteria:- Must have received a subretinal injection of RetinoStat
- Must have been enrolled in Protocol RS1/001/10
Exclusion Criteria:
- Did not receive RetinoStat® as part of the RS1/001/10 protocol