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The purpose of this study is to assess the safety and efficacy of Bimatoprost/Timolol Fixed Combination in patients with glaucoma or ocular hypertension
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Bel Air, Maryland, United States
Vienna, Austria
Montreal, Quebec, Canada
Berlin, Germany
Start Date
May 1, 2003
Primary Completion Date
September 1, 2004
Completion Date
September 1, 2004
Last Updated
May 30, 2011
445
ACTUAL participants
bimatoprost/timolol fixed combination
DRUG
Lead Sponsor
Allergan
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT07218796