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Completed Phase 2 Interventional Results available

A Research Study To See How Well an Eye Drop, SURF-100 (A Mycophenolic Acid/Betamethasone Sodium Phosphate Combination), Works and What Side Effects There Are in Subjects With Dry Eye Disease

ClinicalTrials.gov ID: NCT04734197

Public ClinicalTrials.gov record NCT04734197. 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 1, 2026, 11:40 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 Multicenter, Randomized, Double-Masked Study To Evaluate The Safety, Tolerability, And Efficacy Of SURF-100 Ophthalmic Solution (A Mycophenolic Acid/Betamethasone Sodium Phosphate Combination) In Subjects With Dry Eye Disease

Brief summary

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

SURF-100 is being studied for the treatment of dry eye disease. SURF-100 is an investigational drug (which means the study drug is currently being tested) in the form of a sterile eye drop. The purpose of this research study is to see how well SURF-100 works to treat dry eye and what potential side effects there are, and to compare it with Vehicle (placebo), 0.1% mycophenolic acid (MPA) in Vehicle, 0.3% MPA in Vehicle, 0.01% betamethasone phosphate (BSP) in Vehicle, Restasis and Xiidra. This study will involve about 280-350 study participants age 18 and older at about 40 different research sites in the United States.

Study identification

NCT ID
NCT04734197
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Surface Ophthalmics, Inc.
Industry
Enrollment
349 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
Jan 10, 2021
Primary completion
Mar 24, 2022
Completion
Mar 24, 2022
Last update posted
May 10, 2025

2021 – 2022

United States locations

U.S. sites
40
U.S. states
17
U.S. cities
36
Facility City State ZIP Site status
Cornea and Cataract Consultants of Arizona PC Phoenix Arizona 85032
Canyon City EyeCare Azusa California 91702
Inland Eye Specialists Hemet California 92545
North Valley Eye Medical Group Inc. Mission Hills California 91345
LoBue Laser and Eye Medical Center Murrieta California 92562
Eye Research Foundation Newport Beach California 92663
Martel Eye Medical Group Rancho Cordova California 95670
Sacramento Eye Consultants, A Medical Corporation Sacramento California 95815
The Eye Center of Northern Colorado Fort Collins Colorado 80528
Connecticut Eye Consultants, PC Danbury Connecticut 06810
Florida Eye Microsurgical Institute, Inc. Boynton Beach Florida 33426
Hernando Eye Institute Brooksville Florida 34613
Bowden Eye and Associates Jacksonville Florida 32256
Eye Center of North Florida PA Panama City Florida 32405
International Research Center Tampa Florida 33603
Blue Ocean Clinical Research at The Macula Center The Villages Florida 32162
Coastal Research Associates, LLC Roswell Georgia 30076
Jackson Eye Lake Villa Illinois 60046
Cincinnati Eye Institute Edgewood Kentucky 41017
Kentucky Eye Institute Lexington Kentucky 40517
Midwest Vision Research Foundation at Pepose Vision Institute Chesterfield Missouri 63017
Tauber Eye Center Kansas City Missouri 64111
Tekwani Vision Center St Louis Missouri 63128
Ophthalmology Consultants Ltd. St Louis Missouri 63131
EyeSight Ophthalmic Services Somersworth New Hampshire 03878
Alterman, Modi & Wolter Poughkeepsie New York 12603
Rochester Ophthalmological Group, PC Rochester New York 14618
Physicians Protocol Greensboro North Carolina 27401
Scott & Christie and Associates, PC Cranberry Township Pennsylvania 16066
Black Hills Regional Eye Institute Rapid City South Dakota 57701
Total Eye Care, PA Memphis Tennessee 38119
VRF Eye Specialty Group Memphis Tennessee 38120
West TN EyeCare dba Toyos Clinic Nashville Tennessee 37215
Texan Eye Care, PA - Keystone Research, Ltd Austin Texas 78731
Houston Eye Associates Houston Texas 77025
Advanced Laser Vision & Surgical Institute Houston Texas 77034
Eye Clinics of South Texas, PA San Antonio Texas 78209
R and R Eye Research, LLC San Antonio Texas 78229
Tanner Clinic Layton Utah 84041
The Eye Institute of Utah Salt Lake City Utah 84107

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

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Other public records listing Dry Eye Disease. Sorted by last update posted; newest first. Not a recommendation.

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About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04734197, 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 May 10, 2025 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04734197 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →