drugset / Trial / NCT00712491

Phase 1/2 Study of an Ocular Sirolimus (Rapamycin) Formulation in Patients With Age-Related Macular Degeneration

NCT00712491

Phase 1/2 Terminated 20 enrolled Santen Inc. MacuSight, Inc. · collab
RandomizedParallel-groupSingle-blindTreatment

Summary

The purpose of this study is to determine the safety and efficacy of an ocular sirolimus (rapamycin) formulation via different injection routes in patients with treatment-naive sub-foveal choroidal neovascularization secondary to age-related macular degeneration.

Timeline

Start
2008-09
Primary completion
2009-11
Completion
2010-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Sirolimus Small molecule 352 ug Subcutaneous
Subject Sirolimus Small molecule 1320 ug Subcutaneous