drugset / Trial / NCT00355446

Bioavailability of Bimatoprost Ophthalmic Solution in Human Aqueous.

NCT00355446

Phase 4 Completed 48 enrolled Indiana University
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to assay human aqueous for bimatoprost and the presence of any metabolites, especially prostaglandin analogs. Hypothesis:Bimatoprost is not metabolized to a prostaglandin F-2-alpha analog in human eyes * Bimatoprost levels in human aqueous peak approximately three hours post dosing

Timeline

Start
2001-07
Primary completion
Completion
2004-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Bimatoprost Other / unclassified 0.03 %

Indications