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Completed Phase 3 Interventional Results available

Effect of NOV03 on Signs and Symptoms of Dry Eye Disease Associated With Meibomian Gland Dysfunction (Mojave Study)

ClinicalTrials.gov ID: NCT04567329

Public ClinicalTrials.gov record NCT04567329. 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 Jul 21, 2026, 11:20 AM 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, Multi-Center, Randomized, Double-Masked, Saline-Controlled Trial to Evaluate the Effect of NOV03 on Signs and Symptoms of Dry Eye Disease Associated With Meibomian Gland Dysfunction (Mojave Study)

Study identification

NCT ID
NCT04567329
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Bausch & Lomb Incorporated
Industry
Enrollment
620 participants

Conditions and interventions

Interventions

  • NOV03 Drug
  • Saline Solution Drug

Drug

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
Nov 17, 2020
Primary completion
Aug 29, 2021
Completion
Aug 29, 2021
Last update posted
Aug 18, 2024

2020 – 2021

United States locations

U.S. sites
35
U.S. states
18
U.S. cities
32
Facility City State ZIP Site status
Bausch Site 206 Phoenix Arizona 85032
Bausch Site 202 Garden Grove California 92843
Bausch Site 221 Hemet California 92545
Bausch Site 214 Inglewood California 90301
Bausch Site 226 Murrieta California 92562
Bausch Site 213 Santa Ana California 92705
Bausch site 236 Westminster California 92683
Bausch site 225 Grand Junction Colorado 81501
Bausch Site 211 Delray Beach Florida 33484
Bausch Site 204 Morrow Georgia 30260
Bausch Site 209 Chicago Illinois 60616
Bausch site 218 Hoffman Estates Illinois 60169
Bausch Site 230 Overland Park Kansas 66210
Bausch Site 207 Louisville Kentucky 40220
Bausch Site 228 Havre de Grace Maryland 21078
Bausch Site 231 Bloomington Minnesota 55431
Bausch Site 229 St Louis Missouri 63128
Bausch Site 224 St Louis Missouri 63131
Bausch Site 217 Washington Missouri 63090
Bausch Site 208 Rochester New York 14618
Bausch Site 210 Asheville North Carolina 28803
Bausch site 233 High Point North Carolina 27262
Bausch site 232 Southern Pines North Carolina 28387
Bausch Site 201 Cincinnati Ohio 45247
Bausch Site 216 Cleveland Ohio 44115
Bausch Site 223 Columbus Ohio 43215
Bausch Site 215 Nashville Tennessee 37215
Bausch site 235 Austin Texas 78731
Bausch Site 219 Cedar Park Texas 78613
Bausch Site 212 League City Texas 77573
Bausch site 234 San Antonio Texas 78209
Bausch Site 222 San Antonio Texas 78215
Bausch Site 203 San Antonio Texas 78230
Bausch Site 220 Norfolk Virginia 23502
Bausch Site 227 Seattle Washington 98119

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 NCT04567329, 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 Aug 18, 2024 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04567329 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →