Study of AR-13324 in Patients With Elevated Intraocular Pressure

PHASE2CompletedINTERVENTIONAL
Enrollment

85

Participants

Timeline

Start Date

March 31, 2012

Primary Completion Date

July 31, 2012

Study Completion Date

July 31, 2012

Conditions
Ocular HypertensionOpen Angle Glaucoma
Interventions
DRUG

AR-13324 Ophthalmic Solution 0.01%

Administered to study eye, once daily (QD) in the morning (AM) for 7 days

DRUG

AR-13324 Ophthalmic Solution 0.02%

Administered to study eye, QD AM for 7 days

DRUG

AR-13324 Ophthalmic Solution 0.04%

Administered to study eye, QD AM for 7 days

OTHER

AR-13324 Ophthalmic Solution Vehicle

Administered to study eye, QD AM for 7 days

Trial Locations (11)

14618

Rochester Ophthalmology Group, Rochester

19107

Wills Eye Hospital, Philadelphia

30076

Coastal Research Associates, LLC, Roswell

37803

Univ Eye Surgeons, Maryville Ctr., Maryville

63090

Comprehensive Eye Care, St Louis

66204

Heart of America Eye Care, P.A., Shawnee Mission

74104

The Eye Institute, Tulsa

78240

Medical Center Ophthalmology Associates, San Antonio

78731

Texan Eye, Austin

92657

Aesthetic Eye Care Institute, Newport Beach

06824

Robert Noecker, M.D., M.B.A., Fairfield

Sponsors
All Listed Sponsors
lead

Aerie Pharmaceuticals

INDUSTRY

NCT01528787 - Study of AR-13324 in Patients With Elevated Intraocular Pressure | Biotech Hunter | Biotech Hunter