Safety and Effects of Brimonidine Intravitreal Implant in Patients With Glaucomatous Optic Neuropathy

PHASE2CompletedINTERVENTIONAL
Enrollment

70

Participants

Timeline

Start Date

September 30, 2008

Primary Completion Date

January 31, 2011

Study Completion Date

August 31, 2011

Conditions
Glaucoma, Open-Angle
Interventions
DRUG

400 ug Brimonidine Implant

400 ug Brimonidine Tartrate Posterior Segment Drug Delivery system; Applicator System at Day 1 in study eye.

DRUG

200 ug Brimonidine Implant

200 ug Brimonidine Tartrate Posterior Segment Drug Delivery system; Applicator System at Day 1 in study eye.

DRUG

Sham (no implant)

Sham Posterior Segment Drug Delivery system; Applicator System at Day 1 in study eye.

Trial Locations (2)

Unknown

Artesia

Tel Aviv

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Allergan

INDUSTRY

NCT00693485 - Safety and Effects of Brimonidine Intravitreal Implant in Patients With Glaucomatous Optic Neuropathy | Biotech Hunter | Biotech Hunter