Trials / Completed
CompletedNCT00856622
A Study Demonstrating The Effect Of Latanoprost In Combination With Timolol, Latanoprost Alone And Timolol Alone On Eye Pressure In Open Angle Glaucoma Or Ocular Hypertension In Patients
A 6-Month, Randomized, Double-Masked Comparison Of Fixed Combination Of Latanoprost And Timolol With The Individual Components, Continuing Into A 6-Month Open Label Safety Study Of Fixed Combination In Patients With Glaucoma Or Ocular Hypertension.
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 436 (actual)
- Sponsor
- Pfizer's Upjohn has merged with Mylan to form Viatris Inc. · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to demonstrate that fixed combination of latanoprost and timolol (PhXA41) has better IOP lowering effect than the individual monotherapies.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | i. Fixed combination of latanoprost 0.005% and timolol 0.5% | one drop in the morning and placebo in the evening |
| DRUG | timolol 0.5% ophthalmic solution | one drop in the morning and evening |
| DRUG | latanoprost 0.005% ophthalmic solution | placebo in the morning and latanoprost .005% in the evening |
Timeline
- Start date
- 1997-08-01
- Primary completion
- 1999-06-01
- Completion
- 1999-06-01
- First posted
- 2009-03-06
- Last updated
- 2021-02-21
Locations
37 sites across 1 country: Germany
Source: ClinicalTrials.gov record NCT00856622. Inclusion in this directory is not an endorsement.