Efficacy and Safety of Travoprost 0.004% Versus Tafluprost 0.0015% in Patients With Primary Open-angle Glaucoma or Ocular Hypertension

PHASE4CompletedINTERVENTIONAL
Enrollment

51

Participants

Timeline

Start Date

September 30, 2009

Primary Completion Date

March 31, 2010

Study Completion Date

March 31, 2010

Conditions
Glaucoma
Interventions
DRUG

Travoprost 0.004% ophthalmic solution (TRAVATAN)

One drop in the qualifying eye(s) each evening at 6:00 PM for 6 weeks, topical administration

DRUG

Tafluprost 0.0015% ophthalmic solution

One drop in the qualifying eye(s) each evening at 6:00 PM for 6 weeks, topical administration

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Alcon Research

INDUSTRY

NCT00966940 - Efficacy and Safety of Travoprost 0.004% Versus Tafluprost 0.0015% in Patients With Primary Open-angle Glaucoma or Ocular Hypertension | Biotech Hunter | Biotech Hunter