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Comparative Study of OPC-1085EL Ophthalmic Solution to Latanoprost Ophthalmic Solution 0.005% in Subjects with Primary Open-Angle Glaucoma or Ocular Hypertension (Phase 3 study)

Comparative Study of OPC-1085EL Ophthalmic Solution to Latanoprost Ophthalmic Solution 0.005% in Subjects with Primary Open-Angle Glaucoma or Ocular Hypertension (Phase 3 study)

Status
Unknown
Phases
Phase 3
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT2080222437
Enrollment
220
Registered
2014-03-26
Start date
2014-03-26
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Glaucoma or ocular hypertension

Interventions

Sponsors

Otsuka Pharmaceutical Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Subjects with bilateral primary open-angle glaucoma or ocular hypertension

Exclusion criteria

Exclusion criteria: Subjects with ocular conditions as defined by the protocol

Design outcomes

Primary

MeasureTime frame
Intraocular pressure

Secondary

MeasureTime frame
Efficacy: Intraocular pressure Safety

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026