Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT06444529 · ClinicalTrials.gov registry record · Phase 3

A Double-Masked Comparison of FID 123320 Ophthalmic Solution to Vehicle for the Reduction of Ocular Redness

A Phase 3 study, sponsored by Alcon Research.

Completed
Registry status
Phase 3
Development phase
159
Enrollment target

NCT06444529: Completed Phase 3 study, sponsored by Alcon Research.

NCT06444529 is a Phase 3 study that has completed, run by Alcon Research. The registered enrollment target is 159 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (79% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT06444529, a Phase 3 study, has completed, sponsored by Alcon Research.

COMPLETED
Registry status
Phase 3
Development phase
159 participants
Enrollment target

Study Summary

The purpose of this study is to assess the safety and efficacy of Apraclonidine Hydrochloride Ophthalmic Solution 0.125% when compared to Vehicle, in relieving redness of the eye due to minor eye irritations. This study will be conducted in the United States.

Primary Outcome

Ocular redness will be assessed by the investigator using a scale from 0 to 4 in half-unit increments (0=none; 4=extremely severe). This endpoint is co-primary with the 10 hours post-instillation endpoint.

Interventions

  • DRUG Vehicle
  • DRUG Apraclonidine Hydrochloride Ophthalmic Solution

Trial Details

FieldValue
Enrollment Target 159 participants
Start Date 2024-08-21
Est. Completion 2025-01-08
Phase Phase 3
Alcon Research

275 total trials

What the finished NCT06444529 record still lists

NCT06444529 is an interventional study that assigns participants to a tested intervention. The registered 159 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (79% lower).

The record links to 0 conditions, and to 2 interventions - of which Vehicle is the first listed.

NCT06444529 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06444529 about?

NCT06444529 is a clinical study titled "A Double-Masked Comparison of FID 123320 Ophthalmic Solution to Vehicle for the Reduction of Ocular Redness". The purpose of this study is to assess the safety and efficacy of Apraclonidine Hydrochloride Ophthalmic Solution 0.125% when compared to Vehicle, in relieving redness of the eye due to minor eye irritations. This study will be conducted in the United States.

What is the current status of trial NCT06444529?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 159 participants. The study started on 2024-08-21. Estimated completion is 2025-01-08.

What interventions are being tested in trial NCT06444529?

The interventions under investigation include: Vehicle (DRUG), Apraclonidine Hydrochloride Ophthalmic Solution (DRUG).

Who is sponsoring clinical trial NCT06444529?

This trial is sponsored by Alcon Research, which has 275 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06444529's enrollment target sits among peer trials

159 1501st of 2000 higher than 499 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT05267626 · 159 participants · Phase 1

    Study of AU-007, A Monoclonal Antibody That Binds to IL-2 and Inhibits IL-2Rα Binding, in Patients With Unresectable Locally Advanced or Metastatic Cancer

  • NCT06321575 · 159 participants · NA

    The Golazo® Peripheral Atherectomy System for a Safe and Effective Atherectomy (GREAT Trial)

  • NCT06729151 · 159 participants

    Effect of Intradetrusor onabotulinumtoxinA Injection Versus Conservative Management on Female Sexual Function in Patients With Bladder Pain Syndrome

  • NCT07023731 · 159 participants · Phase 1

    A Study to Evaluate ARV-806 in Adults With Advanced Cancer That Has the KRAS G12D Mutation

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT06444529, the US trial registry maintained by the National Library of Medicine. NCT06444529 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.