Clinical Trials Directory

Trials / Completed

CompletedNCT00347841

Efficacy of Bimatoprost 0.03% in Patients Who Are Low-Responders to Latanoprost

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
Sponsor
Innovative Medical · Industry
Sex
All
Age
18 Years
Healthy volunteers

Summary

To evaluate the IOP-lowering efficacy of bimatoprost 0.03% in patients found to be low-responders to latanoprost therapy.

Conditions

Interventions

TypeNameDescription
DRUGBimatoprost 0.03%, Latanoprost

Timeline

First posted
2006-07-04
Last updated
2007-06-01

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00347841. Inclusion in this directory is not an endorsement.