drugset / Trial / NCT01280669

Intravitreal Sirolimus as Therapeutic Approach to Uveitis

NCT01280669 ↗

RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to find out about the safety and effectiveness of two different doses the study drug, sirolimus, administered intravitreally in patients with uveitis. The potential effectiveness of sirolimus can be utilized to control inflammation in uveitis and yet avoid the potential complications that are usually associated with the systemic use of the drug and other immunomodulatory therapies. In this study, the investigators will administer sirolimus inside the eye (intravitreally) in one of two doses (440mcg/mcL or 880mcg/mcL). Local administration of sirolimus to the eye is not expected to have effects on the rest of the body. Therefore, it may offer a safer way than the current methods used to control the inflammation caused by non-infectious uveitis.

Timeline

Start
2022-09
Primary completion
2024-09
Completion
2024-12

Outcome

Outcome not reported

Stopped (Business): “Never started due to sponsor decision”

Drugs

EvaluationDrugModalityDoseRoute
Subject Sirolimus Small molecule 440 ug Intravitreal
Subject Sirolimus Small molecule 880 ug Intravitreal