drugset / Trial / NCT01257607

Safety and Efficacy Study of MIM-D3 Ophthalmic Solution for the Treatment of Dry Eye

NCT01257607 ↗

Phase 2 Completed 150 enrolled Mimetogen Pharmaceuticals USA, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

The objective of this study is to compare the safety and efficacy of 1% MIM-D3 and 5% MIM-D3 to placebo for the treatment of the signs and symptoms of dry eye.

Timeline

Start
2010-11
Primary completion
2011-05
Completion
2011-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Tavilermide Protein / enzyme biologic 1 % Other
Subject Tavilermide Protein / enzyme biologic 5 % Other

Indications