A Safety and Efficacy Study of a New Eye Drop Formulation in Patients With Dry Eye Disease.

PHASE3CompletedINTERVENTIONAL
Enrollment

242

Participants

Timeline

Start Date

January 6, 2016

Primary Completion Date

September 9, 2016

Study Completion Date

September 9, 2016

Conditions
Dry Eye Syndromes
Interventions
DRUG

Carboxymethylcellulose Based Eye Drop

Carboxymethylcellulose based eye drop (OM3 Tear) administered as 1-2 drops in each eye, as needed, at least 2 times daily for 90 days.

DRUG

Carboxymethylcellulose Sodium 0.5%

Carboxymethylcellulose sodium 0.5% (REFRESH OPTIVE® ADVANCED) administered as 1-2 drops in each eye, as needed, at least 2 times daily for 90 days.

Trial Locations (13)

14618

Rochester Ophthalmological Group, PC, Rochester

16066

Scott and Christie and Associate, Cranberry Township

28210

Charlotte Eye Ear Nose, Charlotte

63131

Ophthalmology Associates, St Louis

64154

Moyes Eye Center, PC, Kansas City

78731

Texan Eye, Austin

91204

Lugene Eye Institute, Glendale

91506

Havana Research Institute LLC, Burbank

91702

The Private Practice of Milton Hom, OD, Azusa

92123

Eric M. White, OD, INC, San Diego

VIC 3010

Department of Optometry & Vision Sciences, The University of Melbourne, Parkville

NSW 2031

Prof. M.T. Coroneo Pty. Ltd., Randwick

NSW 2052

The University of New South Wales School of Optometry and Vision Science, Sydney

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Allergan

INDUSTRY

NCT02553772 - A Safety and Efficacy Study of a New Eye Drop Formulation in Patients With Dry Eye Disease. | Biotech Hunter | Biotech Hunter