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Completed Phase 2 Interventional

A 28 Day Study of ONO-9054 Ophthalmic Solution in Subjects With Ocular Hypertension (OHT) or Open-angle Glaucoma (OAG)

ClinicalTrials.gov ID: NCT02083289

Public ClinicalTrials.gov record NCT02083289. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 28, 2026, 7:50 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A 28-day Double-masked, Randomized, Parallel-group, Active Controlled Study of ONO-9054 Ophthalmic Solution in Subjects With Ocular Hypertension (OHT) or Open-angle Glaucoma (OAG)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The primary objectives of this study are to compare the safety, tolerability, and mean change from baseline in diurnal intraocular pressure (IOP) of ONO-9054 30 µg/mL (0.003%) to latanoprost 0.005% following ocular instillation once every evening for 28 days.

Study identification

NCT ID
NCT02083289
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Ono Pharmaceutical Co., Ltd.
Industry
Enrollment
123 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 85 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 2014 (Type not available)
Primary completion
Dec 2014 (Actual)
Completion
Not listed
Last update posted
Feb 25, 2016

Started 2014

United States locations

U.S. sites
12
U.S. states
6
U.S. cities
12
Facility City State ZIP Site status
Los Angeles Clinical Site Los Angeles California 90048 —
Mission Hills Clinical Site Mission Hills California 91345 —
Newport Beach Clinical Site Newport Beach California 92663 —
Pasadena Clinical Site Pasadena California 91105 —
Petaluma Clinical Site Petaluma California 94954 —
Morrow Clinical Site Morrow Georgia 30260 —
Roswell Clinical Site Roswell Georgia 30076 —
New York Clinical Site New York New York 10029 —
High Point Clinical Site High Point North Carolina 27262 —
Cranberry Township Clinical Site Cranberry Township Pennsylvania 16066 —
Philadelphia Clinical Site Philadelphia Pennsylvania 19104 —
Austin Clinical Site Austin Texas 78731 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02083289, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 25, 2016 · Synced Oct 28, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02083289 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →