drugset / Trial / NCT01461213

Summary

\- Primary objective: To assess the safety and tolerability of the AAV.REP1 vector, administered at two different doses to the retina in 12 patients with a diagnosis of choroideremia. \- Secondary Objective: To identify any therapeutic benefit as evidenced by a slowing down of the retinal degeneration assessed by functional and anatomical methods in the treated eye compared to the control eye 24 months after gene delivery.

Timeline

Start
2011-10
Primary completion
2017-10
Completion
2017-10

Drugs

EvaluationDrugModalityDoseRoute
Subject rAAV2.REP1 Gene therapy (AAV / viral vector) 1e+10 vg Other
Subject rAAV2.REP1 Gene therapy (AAV / viral vector) 1e+11 vg Other

Indications