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Recruiting Phase 3 Interventional

Bioequivalence Study With Clinical Endpoint Comparing Bimatoprost Ophthalmic Solution 0.01% and LUMIGAN® in the Treatment of Chronic Open-Angle Glaucoma or Ocular Hypertension in Both Eyes.

ClinicalTrials.gov ID: NCT05401357

Public ClinicalTrials.gov record NCT05401357. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 23, 2026, 8:41 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-blind, Multiple Dose, Parallel-group, Two-arm, Multicenter, Bioequivalence Study With Clinical Endpoint Comparing Bimatoprost Ophthalmic Solution 0.01% and LUMIGAN® (Bimatoprost Ophthalmic Solution) 0.01% in the Treatment of Subjects With Chronic Open-angle Glaucoma or Ocular Hypertension in Both Eyes

Study identification

NCT ID
NCT05401357
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Amneal Pharmaceuticals, LLC
Industry
Enrollment
168 participants

Conditions and interventions

Interventions

  • Test - Bimatoprost 0.01% Ophthalmic Solution Drug
  • Reference - LUMIGAN® (Bimatoprost 0.01% Ophthalmic Solution) Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 28, 2022
Primary completion
Nov 30, 2022
Completion
Nov 30, 2022
Last update posted
Aug 9, 2022

2022

United States locations

U.S. sites
9
U.S. states
6
U.S. cities
9
Facility City State ZIP Site status
Eye Research Foundation Inc. Newport Beach California 92663 Recruiting
North Bay Eye Associates, Inc. Petaluma California 94954 Recruiting
Volusia Eye Associates New Smyrna Beach Florida 32169 Recruiting
Clayton Eye Clinical Research, LLC Morrow Georgia 30260 Recruiting
Coastal Research Associates, LLC Roswell Georgia 30076 Recruiting
Toyos Clinic Nashville Tennessee 37215 Recruiting
Keystone Research Austin Texas 78731 Not yet recruiting
Houston Eye Associates, North Loop Houston Texas 77008 Recruiting
Cheyenne Eye Clinic & Surgery Center Cheyenne Wyoming 82001 Recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05401357, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 9, 2022 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05401357 live on ClinicalTrials.gov.

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