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NCT03896633 · ClinicalTrials.gov registry record · Phase 1

Therapeutic Equivalence Study of Generic Brinzolamide vs Azopt

A Phase 1 study of Glaucoma and Open Angle or Ocular Hypertension, sponsored by Bausch & Lomb Incorporated.

Completed
Registry status
Phase 1
Development phase
637
Enrollment target
1
Study location

NCT03896633: Completed Phase 1 study of Glaucoma and Open Angle or Ocular Hypertension, sponsored by Bausch & Lomb Incorporated.

NCT03896633 is a Phase 1 study of Glaucoma and Open Angle or Ocular Hypertension that has completed, run by Bausch & Lomb Incorporated. The registered enrollment target is 637 participants, below the 904-participant average among 92 other Glaucoma trials with a reported enrollment target (30% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03896633, a Phase 1 study of Glaucoma and Open Angle or Ocular Hypertension, has completed, sponsored by Bausch & Lomb Incorporated.

COMPLETED
Registry status
Phase 1
Development phase
637 participants
Enrollment target
1
Study location

Study Summary

The main purpose of this prospective study is to demonstrate the therapeutic equivalence of topical brinzolamide compared with AzoptTM

Interventions

  • DRUG brinzolamide 1% ophthalmic suspension
  • DRUG Azopt 1%

Study Locations (1)

New Jersey

  • Various - Bridgewater

Trial Details

FieldValue
Enrollment Target 637 participants
Start Date 2018-02-28
Est. Completion 2018-11-17
Phase Phase 1

Sponsor

Bausch & Lomb Incorporated

174 total trials

What the Registry Record Tells You About NCT03896633

The ClinicalTrials.gov registry entry for NCT03896633 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 637 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 904-participant average among 92 other Glaucoma trials with a reported enrollment target (30% lower). The listed sponsor is Bausch & Lomb Incorporated, which has 174 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Glaucoma appearing as the primary indexed condition, and to 2 interventions - of which brinzolamide 1% ophthalmic suspension is the first listed.

NCT03896633 reports 1 study location spanning 1 distinct geographic area - top geographies include New Jersey.

Frequently Asked Questions

What is clinical trial NCT03896633 about?

NCT03896633 is a clinical study titled "Therapeutic Equivalence Study of Generic Brinzolamide vs Azopt". The main purpose of this prospective study is to demonstrate the therapeutic equivalence of topical brinzolamide compared with AzoptTM

What is the current status of trial NCT03896633?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 637 participants. The study started on 2018-02-28. Estimated completion is 2018-11-17.

What conditions does trial NCT03896633 study?

This clinical trial studies the following conditions: Glaucoma, Open Angle or Ocular Hypertension.

What interventions are being tested in trial NCT03896633?

The interventions under investigation include: brinzolamide 1% ophthalmic suspension (DRUG), Azopt 1% (DRUG).

Who is sponsoring clinical trial NCT03896633?

This trial is sponsored by Bausch & Lomb Incorporated, which has 174 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03896633 being conducted?

This trial has 1 study location across New Jersey. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, the data changelog, or report a data error.