Safety/Efficacy Study: OPA-6566 Ophthalmic Solution in Subjects With Primary Open-Angle Glaucoma or Ocular Hypertension

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

160

Participants

Timeline

Start Date

September 30, 2011

Primary Completion Date

October 31, 2012

Study Completion Date

October 31, 2012

Conditions
Primary Open-angle GlaucomaOcular Hypertension
Interventions
DRUG

OPA-6566

OPA-6566, 2 dosing schedules (one drop once per day for 2 weeks and twice per day for 2 weeks)

DRUG

Placebo

Placebo, 2 dosing schedules (one drop once per day for 2 weeks and twice per day for 2 weeks)

DRUG

Latanoprost

Latanoprost (one drop once per day for 4 weeks)

Trial Locations (9)

27262

High Point

30076

Roswell

37803

Maryville

40217

Louisville

63090

Washington

78240

San Antonio

78731

Austin

90701

Artesia

91205

Glendale

Sponsors
All Listed Sponsors
collaborator

Otsuka Pharmaceutical Co., Ltd.

INDUSTRY

lead

Kubota Vision Inc.

INDUSTRY