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STUDY TO DETERMINE THE THERAPEUTIC EQUIVALENCE OF GENERIC BRINZOLAMIDE 1% OPHTHALMIC SUSPENSION MANUFACTURED BY INNOPHARMA INC

Phase 3
Conditions
Health Condition 1: null- PATIENTS WITH PRIMARY OPEN ANGLE GLAUCOMA OR OCULAR HYPERTENSIO
Registration Number
CTRI/2012/03/002494
Lead Sponsor
InnoPharma Inc
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Other (Terminated)
Sex
Not specified
Target Recruitment
286
Inclusion Criteria

1.Male and females 18 years of age or older, diagnosed with primary open-angle glaucoma or ocular hypertension (including pigment dispersion syndrome).

2.If of child bearing potential -

•Must use a reliable means of contraception for the duration of the study or surgically sterilized.

•Must have a negative pregnancy test.

•Must be non-lactating

3.9 am IOP measurements >= 24 <= 36 mmHg, inclusive, in at least one eye, at two eligibility visits separated by one week

4.The IOP criteria to be met by the same eye

5.Visual Acuity of 6/24 or better(or its equivalent by logMAR) in both eyes

6.Gonioscopy angle of >= 3 in both eyes

7.Patients with a level of understanding and willingness to fully comply with all visits and study procedures scheduled by the study site as evidenced by written informed consent

Exclusion Criteria

1.Patients with any form of glaucoma other than open-angle glaucoma

2.Patients with Schaffer angle grade 3 (overall, however occludable angles treated with patent iridectomy are allowed )

3.Patients with a cup/disc ratio greater than 0.8

4.Patients with severe central visual field loss

5.Best corrected VA score worse than 20/200 Snellen (equivalent to +1.0 log Mar)

6.Chronic, recurrent or severe inflammatory eye disease (blepharitis or clinically non-significant conjunctival hyperaemia allowed)

7.Clinically significant or progressive retinal disease or optic nerve disease from any cause apart from glaucoma

8.Other ocular pathology especially Fuchâ??s endothelial dystrophy, moderate to severe guttata, subjectively low endothelial cell count by slit lamp biomicrscopy or any abnormality preventing reliable applanation tonometry

9.Recent, current, or anticipated treatment with any medication that augments adrenergic

responses, or precludes use of an alpha-adrenergic agonist like MAO inhibitors.

10.History of hypersensitivity to oral or topical CAIs, sulfonamide drugs or to any

component of these medications or the study medications or ingredients

11.Contact lens use during the active treatment portion of the trial. However if patient agrees to avoid use of contact lens use 15 minutes before and after drug administration, such patient can be included

12.Active ocular allergies.

13.Conventional ocular surgery or laser surgery within the 3 months prior to visit 1.

14.Any concurrent infectious/non infectious conjunctivitis, keratitis or uveitis.

15.Active ocular diseases or uncontrolled systemic disease. Patients requiring concomitant aggressive therapy with antihypertensives or steroids or patients on oral CAIs like acetazolamide or methazolamide. However patients on stable dose of antihypertensive therapy or stable doses of dermal or inhaled steroids can be allowed

16.Pregnant or nursing mothers and females of childbearing potential not practicing a

reliable and medically acceptable method of birth control

17.Participation in any study during past 30 days

18.Relative or employee of the treating investigator

Study & Design

Study Type
BA/BE
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To establish that the generic Brinzolamide 1% ophthalmic suspension from InnoPharma Inc is therapeutically equivalent to the currently marketed Azoptâ?¢ (Brinzolamide 1% ophthalmic suspension).Timepoint: To establish that the generic Brinzolamide 1% ophthalmic suspension from InnoPharma Inc is therapeutically equivalent to the currently marketed Azoptâ?¢ (Brinzolamide 1% ophthalmic suspension).
Secondary Outcome Measures
NameTimeMethod
To evaluate the safety and efficacy of Brinzolamide 1% ophthalmic suspension in patients with primary open angle glaucoma or ocular hypertensionTimepoint: NA
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