A Study of AR-12286 in Patient With Elevated Intraocular Pressure (IOP)

Elevated Intraocular Pressure Clinical Trial

Official title:

A Phase 2, Double-masked, Randomized, Placebo-controlled, Dose-response Study Assessing the Safety and Ocular Hypotensive Efficacy of AR-12286 Ophthalmic Solution 0.05%, 0.1% and 0.25% in Patients With Elevated Intraocular Pressure

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00902200
• Other study ID #: AR-12286-CS201
• Status: Completed
• Phase: Phase 2
• First received: May 13, 2009
• Last updated: March 25, 2014
• Start date: May 2009
• Est. completion date: September 2009

Study information

• Verified date: March 2014
• Source: Aerie Pharmaceuticals
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

Double-masked, randomized, multi-center, placebo-controlled parallel-comparison of AR-12286.

Description:

Subjects will be randomized to receive AR-12286 Ophthalmic Solution 0.05%, 0.1%, and 0.25% or its vehicle (one eye), q.d. (AM) x 7 days, then q.d. (PM) x 7 days, then b.i.d. x 7 days. The first dose will be administered in the clinic. Ocular safety and ocular hypotensive efficacy will be evaluated in the clinic throughout this period.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 89
• Est. completion date: September 2009
• Est. primary completion date: September 2009
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. 18 years of age or greater.

2. Diagnosis of open angle glaucoma (OAG) or ocular hypertension (OHT). Unmedicated (post-washout, if required) IOP >= 24 mm Hg in one or both eyes at 08:00 hours, >= 21 mm Hg at 10:00, 12:00 and 16:00 hours on post-washout measurement (Visit 1).

3. Corrected visual acuity in each eye +1.0 logMAR (logarithm mininum angle of resolution) or better by ETDRS (Early Treatment Diabetic Retinopathy Study) in each eye (equivalent to 20/200).

4. Able and willing to give signed informed consent and follow study instructions.

Exclusion Criteria:

Either eye

1. Intraocular pressure > 36 mm Hg

2. Known hypersensitivity to any component of the formulation or to topical anesthetics, (benzalkonium chloride, etc.)

3. Ocular trauma within the past six months, or ocular surgery or laser treatment within the past three months.

4. History or evidence of ocular infection inflammation, or of herpes simplex keratitis, or clinically significant blepharitis or conjunctivitis at baseline (Visit 1)..

5. Contact lens wear within 30 minutes of instillation of study medication.

6. Ocular medication of any kind within 30 days of Visit 2, with the exception of a) ocular hypotensive medications (which must be washed out according to the provided schedule), b) lid scrubs (which may be used prior to, but not after Visit 2) or c) lubricating drops for dry eye (which may be used throughout the study),

7. Clinically significant ocular disease (e.g. corneal edema, uveitis, severe keratoconjunctivitis sicca) which might interfere with the study, including glaucomatous damage so severe that washout of ocular hypotensive medications for one month is not judged safe (i.e., cup-disc ratio > 0.8).

8. Central corneal thickness greater than 600 microns.

9. Any abnormality preventing reliable applanation tonometry.

Study eye:

10. Glaucoma: pseudoexfoliation or pigment dispersion component, history of angle closure.

Note: Previous laser peripheral iridotomy is acceptable.

11. Previous glaucoma intraocular surgery or laser procedures in study eye(s).

12. Refractive surgery in study eye(s) (e.g., radial keratotomy, PRK (photorefractive keratectomy), LASIK (Laser-Assisted in situ Keratomileusis), etc.).

General/Systemic:

13. Clinically significant abnormalities in laboratory tests at screening (See Appendix 1).

14. Clinically significant systemic disease (e.g., uncontrolled diabetes, myasthenia gravis, hepatic, renal, cardiovascular or endocrine disorders) which might interfere with the study.

15. Participation in any investigational study within the past 30 days.

16. Changes of systemic medication during the study that could have a substantial effect on IOP within 30 days prior to screening, or anticipated during the study.

17. Due to status of preclinical safety program, women of childbearing potential who are pregnant, nursing, planning a pregnancy, or not using a medically acceptable form of birth control. An adult woman is considered to be of childbearing potential unless she is one year post-menopausal or three months post-surgical sterilization. All females of childbearing potential must have a negative urine pregnancy test result at the screening examination and must not intend to become pregnant during the study.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Elevated Intraocular Pressure
• Glaucoma

Intervention

Drug:
• AR-12286
See arms
• AR-12286 vehicle
See arms

Locations

Country	Name	City	State
United States	Texan Eye	Austin	Texas
United States	Hernando Eye Institute	Brooksville	Florida
United States	Mundorf Practice	Charlotte	North Carolina
United States	Taustine Eye Center	Louisville	Kentucky
United States	Soilsh Practice	Pasadena	California
United States	Bacharach practice	Petaluma	California
United States	Black Hills Regional Eye Institute	Rapid City	South Dakota
United States	Medical Center Ophthalmology Associates	San Antonio	Texas

Sponsors (1)

Lead Sponsor	Collaborator
Aerie Pharmaceuticals

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The primary efficacy endpoint will be mean diurnal IOP on each day at which diurnal IOP is measured at each timepoint.		3 weeks	No