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NCT06267274 · ClinicalTrials.gov registry record · Phase 1

A Randomized, Double-blind, Parallel-group, Two-arm, Multiple Dose, Multicenter, Bioequivalence Study With Clinical Endpoint in the Treatment of Subjects With Chronic Open-angle Glaucoma or Ocular Hypertension in Both Eyes

A Phase 1 study of Ocular Hypertension and Open Angle Glaucoma, sponsored by Amneal Pharmaceuticals.

Recruiting
Registry status
Phase 1
Development phase
240
Enrollment target
4
Study locations

NCT06267274 is a Phase 1 study of Ocular Hypertension and Open Angle Glaucoma that is actively recruiting participants, run by Amneal Pharmaceuticals. The registered enrollment target is 240 participants, below the 274-participant average among 54 other Ocular Hypertension trials with a reported enrollment target (12% lower). The trial reports 4 study locations across 3 states.

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The verdict

NCT06267274, a Phase 1 study of Ocular Hypertension and Open Angle Glaucoma, is actively recruiting participants, sponsored by Amneal Pharmaceuticals.

RECRUITING
Registry status
Phase 1
Development phase
240 participants
Enrollment target
4
Study locations

Study Summary

A randomized, double-blind, parallel-group, two-arm, multiple dose, multicenter, clinical endpoint bioequivalence study

Interventions

  • DRUG Bimatoprost Ophthalmic Solution, 0.01%
  • DRUG LUMIGAN® (bimatoprost ophthalmic solution) 0.01%

Study Locations (4)

California

  • West Coast Eye Institute - Bakersfield
  • Eye Research Foundation - Newport Beach

Georgia

  • Clayton Eye Research - Morrow

Texas

  • Houston Eye Associates - Houston

Trial Details

FieldValue
Enrollment Target 240 participants
Start Date 2024-04-01
Est. Completion 2025-05-01
Phase Phase 1

Sponsor

Amneal Pharmaceuticals

8 total trials

What the Registry Record Tells You About NCT06267274

The ClinicalTrials.gov registry entry for NCT06267274 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 240 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 274-participant average among 54 other Ocular Hypertension trials with a reported enrollment target (12% lower). The listed sponsor is Amneal Pharmaceuticals, which has 8 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Ocular Hypertension appearing as the primary indexed condition, and to 2 interventions - of which Bimatoprost Ophthalmic Solution, 0.01% is the first listed.

NCT06267274 reports 4 study locations spanning 3 distinct geographic areas - top geographies include California, Georgia, Texas.

Frequently Asked Questions

What is clinical trial NCT06267274 about?

NCT06267274 is a clinical study titled "A Randomized, Double-blind, Parallel-group, Two-arm, Multiple Dose, Multicenter, Bioequivalence Study With Clinical Endpoint in the Treatment of Subjects With Chronic Open-angle Glaucoma or Ocular Hypertension in Both Eyes". A randomized, double-blind, parallel-group, two-arm, multiple dose, multicenter, clinical endpoint bioequivalence study

What is the current status of trial NCT06267274?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 240 participants. The study started on 2024-04-01. Estimated completion is 2025-05-01.

What conditions does trial NCT06267274 study?

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

What interventions are being tested in trial NCT06267274?

The interventions under investigation include: Bimatoprost Ophthalmic Solution, 0.01% (DRUG), LUMIGAN® (bimatoprost ophthalmic solution) 0.01% (DRUG).

Who is sponsoring clinical trial NCT06267274?

This trial is sponsored by Amneal Pharmaceuticals, which has 8 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06267274 being conducted?

This trial has 4 study locations across California, Georgia, Texas. 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 Editorial

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