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NCT00586664 · ClinicalTrials.gov registry record · Phase 3

Efficacy and Safety Study of Bepotastine Besilate Ophthalmic Solution in Allergic Conjunctivitis

A Phase 3 study, sponsored by Bausch & Lomb Incorporated.

Completed
Registry status
Phase 3
Development phase
130
Enrollment target

NCT00586664: Completed Phase 3 study, sponsored by Bausch & Lomb Incorporated.

NCT00586664 is a Phase 3 study that has completed, run by Bausch & Lomb Incorporated. The registered enrollment target is 130 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (83% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00586664, a Phase 3 study, has completed, sponsored by Bausch & Lomb Incorporated.

COMPLETED
Registry status
Phase 3
Development phase
130 participants
Enrollment target

Study Summary

Efficacy and safety study of bepotastine besilate ophthalmic solution in allergic conjunctivitis

Primary Outcome

Ocular Itching score: 0=None; 0.5=Intermittent tickle sensation possibly localized in the corner of the eye; 1.0=Intermittent tickle sensation involving more than the corner of the eye; 1.5=Intermittent all-over tickling sensation; 2.0=Mild continuous itch (can be localized) without desire to rub; 2.5=Moderate, diffuse continuous itch with desire to rub; 3.0=Severe itch with desire to rub; 3.5=Severe itch improved with minimal rubbing; 4.0=Incapacitating itch with irresistible urge to rub

Interventions

  • DRUG placebo comparator
  • DRUG Bepreve (bepotastine besilate ophthalmic solution) 1.5%
  • DRUG Bepotastine Besilate Ophthalmic Solution 1.0%

Trial Details

FieldValue
Enrollment Target 130 participants
Start Date 2007-10
Est. Completion 2008-06
Phase Phase 3
Bausch & Lomb Incorporated

174 total trials

What the finished NCT00586664 record still lists

NCT00586664 is an interventional study that assigns participants to a tested intervention. The registered 130 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 (83% lower).

The record links to 0 conditions, and to 3 interventions - of which placebo comparator is the first listed.

NCT00586664 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00586664 about?

NCT00586664 is a clinical study titled "Efficacy and Safety Study of Bepotastine Besilate Ophthalmic Solution in Allergic Conjunctivitis". Efficacy and safety study of bepotastine besilate ophthalmic solution in allergic conjunctivitis

What is the current status of trial NCT00586664?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 130 participants. The study started on 2007-10. Estimated completion is 2008-06.

What interventions are being tested in trial NCT00586664?

The interventions under investigation include: placebo comparator (DRUG), Bepreve (bepotastine besilate ophthalmic solution) 1.5% (DRUG), Bepotastine Besilate Ophthalmic Solution 1.0% (DRUG).

Who is sponsoring clinical trial NCT00586664?

This trial is sponsored by Bausch & Lomb Incorporated, which has 174 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00586664's enrollment target sits among peer trials

130 1594th of 2000 higher than 404 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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Source: ClinicalTrials.gov NCT00586664, the US trial registry maintained by the National Library of Medicine. NCT00586664 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.