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NCT01528787 · ClinicalTrials.gov registry record · Phase 2

Study of AR-13324 in Patients With Elevated Intraocular Pressure

A Phase 2 study, sponsored by Aerie Pharmaceuticals.

Completed
Registry status
Phase 2
Development phase
85
Enrollment target

NCT01528787 is a Phase 2 study that has completed, run by Aerie Pharmaceuticals. The registered enrollment target is 85 participants.

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The verdict

NCT01528787, a Phase 2 study, has completed, sponsored by Aerie Pharmaceuticals.

COMPLETED
Registry status
Phase 2
Development phase
85 participants
Enrollment target

Study Summary

In this double-masked, vehicle-controlled, dose-response study, subjects will be randomized to receive AR-13324 Ophthalmic Solution 0.01%, 0.02%, and 0.04% or its vehicle (one eye), once daily (QD)in the morning (AM) for 7 days. The first dose and last dose will be administered in the clinic. Ocular safety and ocular hypotensive efficacy will be evaluated in the clinic throughout the study.

Interventions

  • DRUG AR-13324 Ophthalmic Solution 0.02%
  • DRUG AR-13324 Ophthalmic Solution 0.04%
  • DRUG AR-13324 Ophthalmic Solution 0.01%
  • OTHER AR-13324 Ophthalmic Solution Vehicle

Trial Details

FieldValue
Enrollment Target 85 participants
Start Date 2012-03
Est. Completion 2012-07
Phase Phase 2

Sponsor

Aerie Pharmaceuticals

32 total trials

What the Registry Record Tells You About NCT01528787

The ClinicalTrials.gov registry entry for NCT01528787 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 85 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Aerie Pharmaceuticals, which has 32 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 4 interventions - of which AR-13324 Ophthalmic Solution 0.02% is the first listed.

NCT01528787 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01528787 about?

NCT01528787 is a clinical study titled "Study of AR-13324 in Patients With Elevated Intraocular Pressure". In this double-masked, vehicle-controlled, dose-response study, subjects will be randomized to receive AR-13324 Ophthalmic Solution 0.01%, 0.02%, and 0.04% or its vehicle (one eye), once daily (QD)in the morning (AM) for 7 days. The first dose and last dose will be administered in the clinic. Ocular...

What is the current status of trial NCT01528787?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 85 participants. The study started on 2012-03. Estimated completion is 2012-07.

What interventions are being tested in trial NCT01528787?

The interventions under investigation include: AR-13324 Ophthalmic Solution 0.02% (DRUG), AR-13324 Ophthalmic Solution 0.04% (DRUG), AR-13324 Ophthalmic Solution 0.01% (DRUG), AR-13324 Ophthalmic Solution Vehicle (OTHER).

Who is sponsoring clinical trial NCT01528787?

This trial is sponsored by Aerie Pharmaceuticals, which has 32 total clinical trials registered on ClinicalTrials.gov.

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.