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OpenTrials
Completed

NCT Number: NCT01722604

Therapeutic Equivalence Study of Generic Brinzolamide vs Azopt

The main purpose of this prospective study is to demonstrate the therapeutic equivalence of topical brinzolamide dosed three times daily compared with AzoptTM (brinzolamide ophthalmic suspension 1%) dosed three times daily in IOP reduction in patients with POAG or OH.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

US01

Louisville, Kentucky, 40217, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male and females 18 years of age or older,
  • diagnosed with primary open-angle glaucoma or ocular hypertension.

Exclusion criteria

  • Patients with any form of glaucoma (such as secondary, congenital, juvenile or normal tension glaucoma, angle closure glaucoma) in either eye other than primary open-angle glaucoma,
  • ocular hypertension.

Treatment and study plan

Brinzolamide 1% ophthalmic suspension

Drug

brinzolamide 1% ophthalmic suspension

Azopt 1%

Drug

Azopt 1%, RLD

Primary outcomes

  1. Intraocular Pressure (IOP) at Week 12

    Time frame: Week 12

Secondary outcomes

  1. Change in Intraocular Pressure (IOP) From Baseline to Week 12

    Time frame: Baseline, Week 12

Sponsors and collaborators

Lead sponsor

Bausch & Lomb Incorporated

Industry

Registry information

Important dates

Study start
2012
Primary completion
2012
Study completion
2012
First posted
Nov 7, 2012
Registry last updated
May 9, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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