At a glance
ClinicalIndex Comparison RecordPhase 3Completed· 188 enrolled
Drug / intervention
OPC-12759 Ophthalmic suspension +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Confirmatory Study of OPC-12759 Ophthalmic Suspension in Dry Eye Patients
In Brief
A Phase 3 clinical trial evaluating OPC-12759 Ophthalmic suspension and Hyalein Mini Ophthalmic solution for Dry Eye Syndromes. Completed, enrolled 188 participants across 5 sites.
Detailed Summary
The purpose of this study is to verify whether OPC-12759 ophthalmic suspension is effective compared with active control in dry eye patients.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsDry Eye Syndromes
CountriesJapan
Collaborators--
Timeline
Phase 3CompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
First PostedApr 2009
Enrollment StartMay 2009
Primary CompletionMar 2010
Study CompletionApr 2010
TodayJul 2026
First PostedApr 21, 2009
Enrollment StartMay 1, 2009
Primary CompletionMar 1, 2010
Study CompletionApr 1, 2010
TodayJul 2, 2026
Enrollment to primary: 10 monthsPosted 17.2 years ago
Interventions
OPC-12759 Ophthalmic suspensiondrug
OPC-12759 Ophthalmic suspension 2%
Hyalein Mini Ophthalmic solutiondrug
Hyalein Mini Ophthalmic solution 0.1%