Safety and Efficacy of TOP1630 for Dry Eye Syndrome

PHASE2CompletedINTERVENTIONAL
Enrollment

69

Participants

Timeline

Start Date

February 20, 2017

Primary Completion Date

June 15, 2017

Study Completion Date

June 15, 2017

Conditions
Dry Eye Syndrome
Interventions
DRUG

TOP1630 Ophthalmic Solution

Bilateral ocular drug administration

DRUG

Placebo to TOP1630 Ophthalmic Solution

Bilateral ocular drug administration

Trial Locations (1)

01810

Andover Eye Associates, Andover

All Listed Sponsors
collaborator

Topivert Pharma Ltd

INDUSTRY

lead

ORA, Inc.

INDUSTRY

NCT03088605 - Safety and Efficacy of TOP1630 for Dry Eye Syndrome | Biotech Hunter | Biotech Hunter