Safety and Efficacy Study of Bimatoprost/Timolol Fixed Combination in Patients With Glaucoma or Ocular Hypertension

Completed · Phase 3

Conditions studied: Ocular Hypertension

In brief

The purpose of this study is to assess the safety and efficacy of Bimatoprost/Timolol Fixed Combination in patients with glaucoma or ocular hypertension

Key facts

Study ID

NCT00332540

Run by

Allergan

People needed

520

Starts

2001-08-01

Expected to finish

2003-08-01

Last updated by the study team

2011-05-30

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Clinical diagnosis of ocular hypertension or chronic glaucoma in both eyes
• Patient requires IOP-lowering drug in both eyes

You may not qualify if…

• Uncontrolled medical condition
• Contraindication to beta-adrenoceptor antagonist therapy

Where it is running

• Study site — Rochester, New York, United States
• Study site — Sherbrooke, Quebec, Canada

Full record on ClinicalTrials.gov

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