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NCT01481077 · ClinicalTrials.gov registry record · Phase 2

A Dose Evaluation Study of the Effect of Plug Placement on the Efficacy and Safety of the Latanoprost Punctal Plug Delivery System (L-PPDS) in Subjects With Ocular Hypertension or Open-Angle Glaucoma

A Phase 2 study, sponsored by Mati Therapeutics.

Completed
Registry status
Phase 2
Development phase
77
Enrollment target

NCT01481077: Completed Phase 2 study, sponsored by Mati Therapeutics.

NCT01481077 is a Phase 2 study that has completed, run by Mati Therapeutics. The registered enrollment target is 77 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (42% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01481077, a Phase 2 study, has completed, sponsored by Mati Therapeutics.

COMPLETED
Registry status
Phase 2
Development phase
77 participants
Enrollment target

Study Summary

The purpose of this study is to determine the effect of plug placement on the efficacy, safety and duration of effect of the L-PPDS (latanoprost punctal plug delivery system).

Interventions

  • DRUG Latanoprost-PPDS

Trial Details

FieldValue
Enrollment Target 77 participants
Start Date 2011-11
Est. Completion 2012-09
Phase Phase 2
Mati Therapeutics

12 total trials

What the finished NCT01481077 record still lists

NCT01481077 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 77 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (42% lower).

The record links to 0 conditions, and to 1 intervention - of which Latanoprost-PPDS is the first listed.

NCT01481077 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01481077 about?

NCT01481077 is a clinical study titled "A Dose Evaluation Study of the Effect of Plug Placement on the Efficacy and Safety of the Latanoprost Punctal Plug Delivery System (L-PPDS) in Subjects With Ocular Hypertension or Open-Angle Glaucoma". The purpose of this study is to determine the effect of plug placement on the efficacy, safety and duration of effect of the L-PPDS (latanoprost punctal plug delivery system).

What is the current status of trial NCT01481077?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 77 participants. The study started on 2011-11. Estimated completion is 2012-09.

What interventions are being tested in trial NCT01481077?

The interventions under investigation include: Latanoprost-PPDS (DRUG).

Who is sponsoring clinical trial NCT01481077?

This trial is sponsored by Mati Therapeutics, which has 12 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01481077's enrollment target sits among peer trials

77 891st of 2000 higher than 1,108 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 NCT01481077, the US trial registry maintained by the National Library of Medicine. NCT01481077 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.