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NCT00332059 · ClinicalTrials.gov registry record · Phase 3
Safety and Efficacy Study of Bimatoprost/Timolol Fixed Combination in Patients With Glaucoma or Ocular Hypertension
A Phase 3 study, sponsored by Allergan.
- Completed
- Registry status
- Phase 3
- Development phase
- 445
- Enrollment target
NCT00332059: Completed Phase 3 study, sponsored by Allergan.
NCT00332059 is a Phase 3 study that has completed, run by Allergan. The registered enrollment target is 445 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (42% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00332059, a Phase 3 study, has completed, sponsored by Allergan.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 445 participants
- Enrollment target
Study Summary
The purpose of this study is to assess the safety and efficacy of Bimatoprost/Timolol Fixed Combination in patients with glaucoma or ocular hypertension
Interventions
- DRUG bimatoprost/timolol fixed combination
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 445 participants |
| Start Date | 2003-05 |
| Est. Completion | 2004-09 |
| Phase | Phase 3 |
What the finished NCT00332059 record still lists
NCT00332059 is an interventional study that assigns participants to a tested intervention. The registered 445 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (42% lower).
The record links to 0 conditions, and to 1 intervention - of which bimatoprost/timolol fixed combination is the first listed.
NCT00332059 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00332059 about?
NCT00332059 is a clinical study titled "Safety and Efficacy Study of Bimatoprost/Timolol Fixed Combination in Patients With Glaucoma or Ocular Hypertension". The purpose of this study is to assess the safety and efficacy of Bimatoprost/Timolol Fixed Combination in patients with glaucoma or ocular hypertension
What is the current status of trial NCT00332059?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 445 participants. The study started on 2003-05. Estimated completion is 2004-09.
What interventions are being tested in trial NCT00332059?
The interventions under investigation include: bimatoprost/timolol fixed combination (DRUG).
Who is sponsoring clinical trial NCT00332059?
This trial is sponsored by Allergan, which has 314 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00332059's enrollment target sits among peer trials
445 864th of 2000 higher than 1,137 of 2,000 other Phase 3 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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