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NCT01881113 · ClinicalTrials.gov registry record · Phase 3

A Multi-Center, Evaluation of the Onset and Duration of Action of AC-170 0.24% Compared to Vehicle

A Phase 3 study of Allergic Conjunctivitis, sponsored by Aciex Therapeutics.

Completed
Registry status
Phase 3
Development phase
101
Enrollment target
1
Study location

NCT01881113 is a Phase 3 study of Allergic Conjunctivitis that has completed, run by Aciex Therapeutics. The registered enrollment target is 101 participants, below the 130-participant average among 20 other Allergic Conjunctivitis trials with a reported enrollment target (22% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT01881113, a Phase 3 study of Allergic Conjunctivitis, has completed, sponsored by Aciex Therapeutics.

COMPLETED
Registry status
Phase 3
Development phase
101 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to evaluate the onset and duration of action of AC-170 0.24% compared to vehicle in the prevention of the signs and symptoms of allergic conjunctivitis in the conjunctival allergen challenge (CAC) model.

Conditions Studied

Interventions

  • DRUG AC-170 0.24%
  • DRUG AC-170 0%

Study Locations (1)

Massachusetts

  • Ora, Inc. - Andover

Trial Details

FieldValue
Enrollment Target 101 participants
Start Date 2013-06
Est. Completion 2013-10
Phase Phase 3

Sponsor

Aciex Therapeutics

8 total trials

What the Registry Record Tells You About NCT01881113

The ClinicalTrials.gov registry entry for NCT01881113 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 101 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 130-participant average among 20 other Allergic Conjunctivitis trials with a reported enrollment target (22% lower). The listed sponsor is Aciex Therapeutics, which has 8 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Allergic Conjunctivitis appearing as the primary indexed condition, and to 2 interventions - of which AC-170 0.24% is the first listed.

NCT01881113 reports 1 study location spanning 1 distinct geographic area - top geographies include Massachusetts.

Frequently Asked Questions

What is clinical trial NCT01881113 about?

NCT01881113 is a clinical study titled "A Multi-Center, Evaluation of the Onset and Duration of Action of AC-170 0.24% Compared to Vehicle". The purpose of this study is to evaluate the onset and duration of action of AC-170 0.24% compared to vehicle in the prevention of the signs and symptoms of allergic conjunctivitis in the conjunctival allergen challenge (CAC) model.

What is the current status of trial NCT01881113?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 101 participants. The study started on 2013-06. Estimated completion is 2013-10.

What conditions does trial NCT01881113 study?

This clinical trial studies the following conditions: Allergic Conjunctivitis.

What interventions are being tested in trial NCT01881113?

The interventions under investigation include: AC-170 0.24% (DRUG), AC-170 0% (DRUG).

Who is sponsoring clinical trial NCT01881113?

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

Where is trial NCT01881113 being conducted?

This trial has 1 study location across Massachusetts. 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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