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NCT01175590 · ClinicalTrials.gov registry record · Phase 3
Safety of Besivance™ (Besifloxacin Ophthalmic Suspension) 0.6% Compared to Vehicle
A Phase 3 study, sponsored by Bausch & Lomb Incorporated.
- Completed
- Registry status
- Phase 3
- Development phase
- 518
- Enrollment target
NCT01175590: Completed Phase 3 study, sponsored by Bausch & Lomb Incorporated.
NCT01175590 is a Phase 3 study that has completed, run by Bausch & Lomb Incorporated. The registered enrollment target is 518 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (33% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01175590, a Phase 3 study, has completed, sponsored by Bausch & Lomb Incorporated.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 518 participants
- Enrollment target
Study Summary
The objective of this study is to evaluate the safety of Besivance (besifloxacin ophthalmic suspension, 0.6%) compared to vehicle.
Primary Outcome
Ocular Treatment-Emergent Adverse Events on the Study Eye
Interventions
- DRUG Vehicle
- DRUG Besivance
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 518 participants |
| Start Date | 2010-06 |
| Est. Completion | 2012-02 |
| Phase | Phase 3 |
What the finished NCT01175590 record still lists
NCT01175590 is an interventional study that assigns participants to a tested intervention. The registered 518 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 (33% lower).
The record links to 0 conditions, and to 2 interventions - of which Vehicle is the first listed.
NCT01175590 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01175590 about?
NCT01175590 is a clinical study titled "Safety of Besivance™ (Besifloxacin Ophthalmic Suspension) 0.6% Compared to Vehicle". The objective of this study is to evaluate the safety of Besivance (besifloxacin ophthalmic suspension, 0.6%) compared to vehicle.
What is the current status of trial NCT01175590?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 518 participants. The study started on 2010-06. Estimated completion is 2012-02.
What interventions are being tested in trial NCT01175590?
The interventions under investigation include: Vehicle (DRUG), Besivance (DRUG).
Who is sponsoring clinical trial NCT01175590?
This trial is sponsored by Bausch & Lomb Incorporated, which has 174 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01175590's enrollment target sits among peer trials
518 723rd of 2000 higher than 1,277 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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