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Not listed Phase 3 Interventional

A Phase 3 Study to Evaluate AZR-MD-001 in Patients with Abnormal Meibomian Gland Function and Dry Eye Disease (DED)

ClinicalTrials.gov ID: NCT06329791

Public ClinicalTrials.gov record NCT06329791. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 26, 2026, 2:48 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3, Multicenter, Vehicle-controlled, Randomized Study to Evaluate the Efficacy, Safety, and Tolerability of AZR-MD-001 in Patients with Abnormal Meibomian Gland Function and Associated Symptoms of Dry Eye Disease (DED)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study is a multicenter, double-masked, vehicle-controlled, randomized, parallel group study designed to evaluate the treatment of abnormal meibomian gland function and associated symptoms of DED using either AZR-MD-001 0.5% ophthalmic ointment or its vehicle. Study drug (either AZR-MD-001 or vehicle) will be dosed twice-weekly at bedtime for up to 12 months.

Study identification

NCT ID
NCT06329791
Recruitment status
Not listed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Azura Ophthalmics
Industry
Enrollment
500 participants

Conditions and interventions

Interventions

Drug · Other

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 28, 2024 (Actual)
Primary completion
Dec 2024 (Estimated)
Completion
Nov 2025 (Estimated)
Last update posted
Sep 27, 2024

2024 – 2025

United States locations

U.S. sites
16
U.S. states
10
U.S. cities
16
Facility City State ZIP Site status
Arizona Eye Center Chandler Arizona 85225 —
Global Research Management, Inc Glendale California 91204 —
Eye Research Foundation Newport Beach California 92663 —
NVISION Clinical Research Torrance California 90505 —
Wyse Eyecare Northbrook Illinois 60062 —
Pankratz Eye Institute Columbus Indiana 47203 —
The Eye Care Institute/Butchertown Clinical Trials Louisville Kentucky 40206 —
Ophthalmology Associates St Louis Missouri 63131 —
NC Eye Associates Apex North Carolina 27502 —
Oculus Research, Inc. Garner North Carolina 27529 —
CORE Shelby North Carolina 28150 —
Scott & Christie and Associates, PC Cranberry Township Pennsylvania 16066 —
Advancing Vision Research (AVR) - Goodlettsville Goodlettsville Tennessee 37072 —
Total Eye Care Memphis Tennessee 38119 —
Advancing Vision Research (AVR) - Smyrna Smyrna Tennessee 37167 —
Piedmont Eye Center Lynchburg Virginia 24502 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06329791, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 27, 2024 · Synced Oct 26, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06329791 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →