Safety Study of 2.0mg Lucentis to Treat Polypoidal Choroidal Vasculopathy

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

20

Participants

Timeline

Start Date

September 30, 2011

Primary Completion Date

February 28, 2015

Study Completion Date

February 28, 2015

Conditions
Polypoidal Choroidal Vasculopathy
Interventions
DRUG

ranibizumab 0.5 or 2.0 mg/0.05 cc

ranibizumab (3:1 ratio of 2mg:0.5 mg ranibizumab) administered in three initial monthly doses followed by a 9 month period of criteria-based, as-needed retreatment and 12 month off drug safety follow up.

Trial Locations (1)

30909

Southeast Retina Center, Augusta

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Genentech, Inc.

INDUSTRY

lead

Southeast Retina Center, Georgia

OTHER

NCT01469156 - Safety Study of 2.0mg Lucentis to Treat Polypoidal Choroidal Vasculopathy | Biotech Hunter | Biotech Hunter