drugset / Trial / NCT01736462

Corneal Endothelial Cell Density Changes, When Mapracorat Ophthalmic Suspension 3%, is Administered for 14 Days

NCT01736462

Phase 1 Completed 61 enrolled Bausch & Lomb Incorporated
NaSingle-groupOpen-label

Summary

The objective of this study is to evaluate the effect on corneal endothelial cell density (cells/mm²) changes at 3 months when mapracorat ophthalmic suspension, 3% is administered QID (four times daily), for 14 days in healthy subjects with a normal ophthalmic history.

Timeline

Start
2013-02
Primary completion
2013-07
Completion
2013-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Mapracorat Small molecule 3 % Other

Indications