drugset / Trial / NCT01055535

Safety and Efficacy Study of Microplasmin in for Non-Surgical Treatment of Focal Vitreomacular Adhesion

NCT01055535 ↗

Phase 2 Completed 17 enrolled ThromboGenics
RandomizedSingle-groupOpen-labelTreatment

Summary

This study will evaluate the safety and efficacy of Microplasmin administered as an intravitreal injection, in subjects with focal vitreomacular adhesion. Ultimately, it is believed that intravitreal microplasmin may offer physicians a safe agent for pharmacologic vitreolysis and induction of Posterior Vitreous Detachment (PVD) without the need for vitrectomy. This clinical study is justified because the study sponsor believes the potential benefits outweigh the potential risks, as outlined below.

Timeline

Start
2010-01
Primary completion
2011-04
Completion
2011-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Ocriplasmin Protein / enzyme biologic 125 ug Intravitreal

Indications

No indication recorded.