A Safety and Efficacy Study of Tavilermide (MIM-D3) Ophthalmic Solution for the Treatment of Dry Eye

PHASE3CompletedINTERVENTIONAL
Enrollment

429

Participants

Timeline

Start Date

December 31, 2015

Primary Completion Date

February 28, 2017

Study Completion Date

March 31, 2017

Conditions
Keratoconjunctivitis Sicca
Interventions
DRUG

1% Tavilermide Ophthalmic Solution

1% Tavilermide BID Dosing

DRUG

Placebo Ophthalmic Solution

Vehicle Ophthalmic Solution

Trial Locations (2)

Unknown

MIM-727 Investigational Site, Louisville

MIM-727 Investigational Site, Nashville

All Listed Sponsors
lead

Mimetogen Pharmaceuticals USA, Inc.

INDUSTRY