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NCT01731002 · ClinicalTrials.gov registry record · Phase 2

Study Comparing the Safety and Efficacy of AR-13324 to Latanoprost in Patients With Elevated Intraocular Pressure

A Phase 2 study, sponsored by Aerie Pharmaceuticals.

Completed
Registry status
Phase 2
Development phase
224
Enrollment target

NCT01731002: Completed Phase 2 study, sponsored by Aerie Pharmaceuticals.

NCT01731002 is a Phase 2 study that has completed, run by Aerie Pharmaceuticals. The registered enrollment target is 224 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (68% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01731002, a Phase 2 study, has completed, sponsored by Aerie Pharmaceuticals.

COMPLETED
Registry status
Phase 2
Development phase
224 participants
Enrollment target

Study Summary

Double-masked, randomized, multi-center, dose-response, active-controlled parallel-comparison of AR-13324 to latanoprost

Primary Outcome

The primary efficacy endpoint was the mean IOP across subjects within treatment group on each day at each post-treatment timepoint. IOP was measured at 0800, 1000, and 1600 hours on days 0, 14, and 28. IOP was also measured at 0800 hours on Day 7 and follow-up days 29 and 30.

Interventions

  • DRUG AR-13324 Ophthalmic Solution 0.02%
  • DRUG Latanoprost ophthalmic solution 0.005%
  • DRUG AR-13324 Ophthalmic Solution 0.01%

Trial Details

FieldValue
Enrollment Target 224 participants
Start Date 2012-11
Est. Completion 2013-05
Phase Phase 2
Aerie Pharmaceuticals

32 total trials

What the finished NCT01731002 record still lists

NCT01731002 is an interventional study that assigns participants to a tested intervention. The registered 224 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (68% higher).

The record links to 0 conditions, and to 3 interventions - of which AR-13324 Ophthalmic Solution 0.02% is the first listed.

NCT01731002 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01731002 about?

NCT01731002 is a clinical study titled "Study Comparing the Safety and Efficacy of AR-13324 to Latanoprost in Patients With Elevated Intraocular Pressure". Double-masked, randomized, multi-center, dose-response, active-controlled parallel-comparison of AR-13324 to latanoprost

What is the current status of trial NCT01731002?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 224 participants. The study started on 2012-11. Estimated completion is 2013-05.

What interventions are being tested in trial NCT01731002?

The interventions under investigation include: AR-13324 Ophthalmic Solution 0.02% (DRUG), Latanoprost ophthalmic solution 0.005% (DRUG), AR-13324 Ophthalmic Solution 0.01% (DRUG).

Who is sponsoring clinical trial NCT01731002?

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

How this trial's enrollment target compares

Where NCT01731002's enrollment target sits among peer trials

224 269th of 2000 higher than 1,727 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01731002, the US trial registry maintained by the National Library of Medicine. NCT01731002 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.