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

Stopped early · Phase 1/Phase 2

Conditions studied: Age-related Macular Degeneration, Choroidal Neovascularization

In brief

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.

Key facts

Study ID

NCT00712491

Run by

Santen Inc.

People needed

20

Starts

2008-09-01

Expected to finish

2010-03-01

Last updated by the study team

2013-01-10

Who can join

Age: 50 and older. Sex: any. Healthy volunteers: not accepted.

You may not qualify if…

• Any other ocular disease that could compromise vision in the study eye
• History of any prior treatment for choroidal neovascularization in the study eye
• Presence of other causes of choroidal neovascularization other than secondary to age-related macular degeneration

Where it is running

• Retinal Consultants of Arizona — Phoenix, Arizona, United States

Full record on ClinicalTrials.gov

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