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NCT00652496 · ClinicalTrials.gov registry record · Phase 2
Safety and Efficacy Study of Different Formulations of Bimatoprost Once-Daily in Patients With Glaucoma or Ocular Hypertension
A Phase 2 study, sponsored by Allergan.
- Completed
- Registry status
- Phase 2
- Development phase
- 249
- Enrollment target
NCT00652496 is a Phase 2 study that has completed, run by Allergan. The registered enrollment target is 249 participants.
The verdict
NCT00652496, a Phase 2 study, has completed, sponsored by Allergan.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 249 participants
- Enrollment target
Study Summary
This study evaluates the safety and efficacy of different formulations of bimatoprost ophthalmic solution compared with Bimatoprost 0.03% once-daily in patients with glaucoma or ocular hypertension. One of the test formulations was given to one eye and bimatoprost 0.03% given to the fellow eye of each patient
Interventions
- DRUG Bimatoprost 0.01% ophthalmic solution
- DRUG Bimatoprost 0.015% formulation 1 ophthalmic solution
- DRUG Bimatoprost 0.015% formulation 2 ophthalmic solution
- DRUG Bimatoprost 0.02% ophthalmic solution
- DRUG Bimatoprost 0.03% ophthalmic solution
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 249 participants |
| Start Date | 2005-01 |
| Est. Completion | 2005-05 |
| Phase | Phase 2 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00652496
The ClinicalTrials.gov registry entry for NCT00652496 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 249 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Allergan, which has 314 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 5 interventions - of which Bimatoprost 0.01% ophthalmic solution is the first listed.
NCT00652496 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00652496 about?
NCT00652496 is a clinical study titled "Safety and Efficacy Study of Different Formulations of Bimatoprost Once-Daily in Patients With Glaucoma or Ocular Hypertension". This study evaluates the safety and efficacy of different formulations of bimatoprost ophthalmic solution compared with Bimatoprost 0.03% once-daily in patients with glaucoma or ocular hypertension. One of the test formulations was given to one eye and bimatoprost 0.03% given to the fellow eye of ea...
What is the current status of trial NCT00652496?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 249 participants. The study started on 2005-01. Estimated completion is 2005-05.
What interventions are being tested in trial NCT00652496?
The interventions under investigation include: Bimatoprost 0.01% ophthalmic solution (DRUG), Bimatoprost 0.015% formulation 1 ophthalmic solution (DRUG), Bimatoprost 0.015% formulation 2 ophthalmic solution (DRUG), Bimatoprost 0.02% ophthalmic solution (DRUG), Bimatoprost 0.03% ophthalmic solution (DRUG).
Who is sponsoring clinical trial NCT00652496?
This trial is sponsored by Allergan, which has 314 total clinical trials registered on ClinicalTrials.gov.
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