Phase 3
Completed N=237
Efficacy and Safety Study of OPC-1085EL Ophthalmic Solution in Subjects With Glaucoma or Ocular Hypertension
Source: ClinicalTrials.gov NCT02105272 ↗Enrolled (actual)
237
Serious AEs
0.0%
Results posted
Nov 2015
Primary outcomePrimary: Decrease From Baseline in Intraocular Pressure — 2.9; 1.6 mmHg
Summary
The purpose of this study is to determine the efficacy and safety of OPC-1085EL ophthalmic solution in comparison with latanoprost ophthalmic solution in subjects who are insufficiently responsive to latanoprost ophthalmic solution.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Decrease From Baseline in Intraocular Pressure |
2.9; 1.6 | — |
| SECONDARY Intraocular Pressure at Week 8 Predose |
17.1; 18.4 | — |
| SECONDARY Intraocular Pressure at Week 8 at 2 Hours After IMP Administration |
17.2; 18.2 | — |
| SECONDARY Intraocular Pressure at Week 8 at 8 Hours After IMP Administration |
16.7; 17.4 | — |
| SECONDARY Decrease From Baseline in Intraocular Pressure at Week 8 at 2 Hours After IMP Administration |
2.1; 1.0 | — |
| SECONDARY Decrease From Baseline in Intraocular Pressure at Week 8 at 8 Hours After IMP Administration |
1.7; 1.0 | — |
Eligibility Criteria
Inclusion Criteria
- Subjects with diagnosis of bilateral primary open-angle glaucoma or ocular hypertension
Exclusion Criteria
- Subjects with ocular conditions as defined by the protocol
Data sourced from ClinicalTrials.gov (NCT02105272). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.