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NCT01863953 · ClinicalTrials.gov registry record · Phase 2

A Safety and Efficacy Study of Fixed-Combination Bimatoprost and Brimonidine in Chronic Glaucoma or Ocular Hypertension

A Phase 2 study of Glaucoma and Ocular Hypertension, sponsored by Allergan.

Completed
Registry status
Phase 2
Development phase
112
Enrollment target
1
Study location

NCT01863953 is a Phase 2 study of Glaucoma and Ocular Hypertension that has completed, run by Allergan. The registered enrollment target is 112 participants, below the 909-participant average among 92 other Glaucoma trials with a reported enrollment target (88% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT01863953, a Phase 2 study of Glaucoma and Ocular Hypertension, has completed, sponsored by Allergan.

COMPLETED
Registry status
Phase 2
Development phase
112 participants
Enrollment target
1
Study location

Study Summary

This is a safety and efficacy study of fixed-combination bimatoprost and brimonidine compared with LUMIGAN® and ALPHAGAN® in patients with chronic glaucoma or ocular hypertension.

Interventions

  • DRUG Vehicle Ophthalmic Solution
  • DRUG Fixed-Combination Bimatoprost/Brimonidine
  • DRUG Bimatoprost Ophthalmic Solution 0.01%
  • DRUG Brimonidine Tartrate Ophthalmic Solution 0.2%

Study Locations (1)

California

  • - Newport Beach

Trial Details

FieldValue
Enrollment Target 112 participants
Start Date 2013-06
Est. Completion 2013-12
Phase Phase 2

Sponsor

Allergan

314 total trials

What the Registry Record Tells You About NCT01863953

The ClinicalTrials.gov registry entry for NCT01863953 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 112 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 909-participant average among 92 other Glaucoma trials with a reported enrollment target (88% lower). The listed sponsor is Allergan, which has 314 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Glaucoma appearing as the primary indexed condition, and to 4 interventions - of which Vehicle Ophthalmic Solution is the first listed.

NCT01863953 reports 1 study location spanning 1 distinct geographic area - top geographies include California.

Frequently Asked Questions

What is clinical trial NCT01863953 about?

NCT01863953 is a clinical study titled "A Safety and Efficacy Study of Fixed-Combination Bimatoprost and Brimonidine in Chronic Glaucoma or Ocular Hypertension". This is a safety and efficacy study of fixed-combination bimatoprost and brimonidine compared with LUMIGAN® and ALPHAGAN® in patients with chronic glaucoma or ocular hypertension.

What is the current status of trial NCT01863953?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 112 participants. The study started on 2013-06. Estimated completion is 2013-12.

What conditions does trial NCT01863953 study?

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

What interventions are being tested in trial NCT01863953?

The interventions under investigation include: Vehicle Ophthalmic Solution (DRUG), Fixed-Combination Bimatoprost/Brimonidine (DRUG), Bimatoprost Ophthalmic Solution 0.01% (DRUG), Brimonidine Tartrate Ophthalmic Solution 0.2% (DRUG).

Who is sponsoring clinical trial NCT01863953?

This trial is sponsored by Allergan, which has 314 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01863953 being conducted?

This trial has 1 study location across California. 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

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, or report a data error.