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Completed Phase 2 Interventional

Study to Evaluate the Safety and Efficacy of Minocycline Ointment in Subjects With Inflamed Meibomian Gland Dysfunction

ClinicalTrials.gov ID: NCT03888378

Public ClinicalTrials.gov record NCT03888378. 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 Sep 5, 2026, 8:55 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 Multi-Center, Double-Masked, Randomized, Vehicle-Controlled Study of the Efficacy and Safety of HY02 Ointment in Subjects With Inflamed Meibomian Gland Dysfunction

Brief summary

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

To evaluate the efficacy and safety of two strengths of HY02 Ointment versus Vehicle administered twice daily for twelve weeks in subjects with a diagnosis of Inflamed Meibomian Gland Dysfunction.

Study identification

NCT ID
NCT03888378
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Hovione Scientia Limited
Industry
Enrollment
270 participants

Conditions and interventions

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
Apr 1, 2019
Primary completion
Sep 17, 2020
Completion
Jan 31, 2021
Last update posted
Mar 4, 2021

2019 – 2021

United States locations

U.S. sites
20
U.S. states
10
U.S. cities
19
Facility City State ZIP Site status
Clinical site - 4 Azusa California 91702
Clinical site - 16 Huntington Beach California 92647
Clinical site - 12 Inglewood California 90301
Clinical site - 13 Mission Hills California 91345
Clinical site 10 Rancho Cordova California 95670
Clinical site - 15 Jacksonville Florida 32256
Clinical Site - 18 Largo Florida 33773
Clinical site - 6 Indianapolis Indiana 46260
Clinical site - 20 New Albany Indiana 47150
Clinical site - 19 Kansas City Missouri 64111
Clinical site - 3 St Louis Missouri 63131
Clinical site - 9 St Louis Missouri 63131
Clinical site - 7 Las Vegas Nevada 89145
Clinical site - 5 Asheville North Carolina 28803
Clinical site - 11 Mason Ohio 45040
Clinical site - 2 Memphis Tennessee 38119
Clinical site - 14 Cedar Park Texas 78613
Clinical Site - 1 El Paso Texas 79902
Clinical site - 8 League City Texas 77573
Clinical site - 17 Norfolk Virginia 23502

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 NCT03888378, 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 Mar 4, 2021 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03888378 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →