drugset / Trial / NCT00749957

Phase 1/2 Safety and Efficacy Study of AAV-RPE65 Vector to Treat Leber Congenital Amaurosis

NCT00749957 ↗

Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of the study is to evaluate the safety and efficacy of an adeno-associated virus vector expressing RPE65 in patients with Leber congenital amaurosis caused by mutations in the RPE65 gene. Funding Source - FDA OOPD

Timeline

Start
2009-06-17
Primary completion
2014-09-23
Completion
2017-09-22

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject rAAV2-CB-hRPE65 Gene therapy (AAV / viral vector) 1.8e+11 vg Other
Subject rAAV2-CB-hRPE65 Gene therapy (AAV / viral vector) 6e+11 vg Other