drugset / Trial / NCT03331770

Efficacy and Tolerability of an Innovative Formulation of BAK-free Latanoprost

NCT03331770

Phase 4 Completed 103 enrolled Laboratorios Poen
NaSingle-groupOpen-labelTreatment

Summary

This study evaluates the efficacy and tolerability of a new formulation of latanoprost without Benzalkonium Chloride (BAK-free). Patients with open-angle glaucoma who were using BAK-containing latanoprost ophthalmic solution for ≥6 months, switched to BAK-free latanoprost ophthalmic emulsion.

Timeline

Start
2017-01-06
Primary completion
2017-10-06
Completion
2017-10-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Latanoprost Small molecule Other

Indications