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COMPLETED Phase 1

Therapeutic Equivalence Study of Generic Brinzolamide vs Azopt

NCT03896633 · View on ClinicalTrials.gov ↗

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

78 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03896633

The ClinicalTrials.gov registry entry for NCT03896633 describes a study currently listed as completed. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 637 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Bausch & Lomb Incorporated, which has 78 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

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. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT03896633 reports 1 study location spanning 1 distinct geographic area — top geographies include New Jersey. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

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. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03896633?

The interventions under investigation include: brinzolamide 1% ophthalmic suspension (DRUG), Azopt 1% (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03896633?

This trial is sponsored by Bausch & Lomb Incorporated, which has 78 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

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.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial