drugset / Trial / NCT00638742

A Phase 1, Open-Label Study of Latanoprost Acid Plasma Concentrations in Pediatric and Adult Glaucoma Patients Treated With Latanoprost.

NCT00638742

Phase 1 Completed 47 enrolled Viatris Inc.
Non-randomizedSingle-groupOpen-labelOther

Summary

To evaluate the steady-state systemic plasma concentrations of latanoprost acid following administration of latanoprost 0.005% (1.5 ug) in pediatric and adult subjects with glaucoma or ocular hypertension.

Timeline

Start
2008-05
Primary completion
2009-03
Completion
2009-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Latanoprost Small molecule 1.5 ug Other