drugset / Trial / NCT00934089

A Phase 2 Study Of The 24-Hour Intraocular Pressure Lowering And Systemic Exposure Of PF-04217329

NCT00934089

Phase 2 Completed 31 enrolled Pfizer
RandomizedCrossoverSingle-blindTreatment

Summary

This study will characterize the effect of PF-04217329, alone and in combination with latanoprost, on circadian intraocular pressure and blood pressure in glaucoma patients. Blood samples will be collected to measure the amount of active metabolite of PF-04217329 in the plasma following dosing.

Timeline

Start
2010-01
Primary completion
2010-06
Completion
2010-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Latanoprost Small molecule Topical
Subject taprenepag isopropyl Small molecule Topical