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NCT01057147 · ClinicalTrials.gov registry record · Phase 2

Safety and Efficacy Study of Rebamipide 2% Ophthalmic Suspension in Subjects With Dry Eye - Effects on Central Cornea

A Phase 2 study, sponsored by Kubota Vision.

Completed
Registry status
Phase 2
Development phase
116
Enrollment target

NCT01057147: Completed Phase 2 study, sponsored by Kubota Vision.

NCT01057147 is a Phase 2 study that has completed, run by Kubota Vision. The registered enrollment target is 116 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (13% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01057147, a Phase 2 study, has completed, sponsored by Kubota Vision.

COMPLETED
Registry status
Phase 2
Development phase
116 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the safety and efficacy of 2% rebamipide compared to placebo in clearing of fluorescein staining of the central cornea in subjects with dry eye disease.

Interventions

  • DRUG rebamipide 2% ophthalmic suspension
  • DRUG placebo eye drops

Trial Details

FieldValue
Enrollment Target 116 participants
Start Date 2010-02
Est. Completion 2011-02
Phase Phase 2
Kubota Vision

16 total trials

What the finished NCT01057147 record still lists

NCT01057147 is an interventional study that assigns participants to a tested intervention. The registered 116 participants enrollment target is mid-sized for trials with a published cap, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (13% lower).

The record links to 0 conditions, and to 2 interventions - of which rebamipide 2% ophthalmic suspension is the first listed.

NCT01057147 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01057147 about?

NCT01057147 is a clinical study titled "Safety and Efficacy Study of Rebamipide 2% Ophthalmic Suspension in Subjects With Dry Eye - Effects on Central Cornea". The purpose of this study is to evaluate the safety and efficacy of 2% rebamipide compared to placebo in clearing of fluorescein staining of the central cornea in subjects with dry eye disease.

What is the current status of trial NCT01057147?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 116 participants. The study started on 2010-02. Estimated completion is 2011-02.

What interventions are being tested in trial NCT01057147?

The interventions under investigation include: rebamipide 2% ophthalmic suspension (DRUG), placebo eye drops (DRUG).

Who is sponsoring clinical trial NCT01057147?

This trial is sponsored by Kubota Vision, which has 16 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01057147's enrollment target sits among peer trials

116 623rd of 2000 higher than 1,375 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT01057147, the US trial registry maintained by the National Library of Medicine. NCT01057147 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.