20089 TA+Lucentis Combo Intravitreal Injections for Treatment of Neovascular Age-related Macular Degeneration (AMD)

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

10

Participants

Timeline

Start Date

September 30, 2010

Primary Completion Date

January 31, 2013

Study Completion Date

January 31, 2013

Conditions
Age-Related Macular DegenerationChoroidal Neovascularization
Interventions
DRUG

IBI-20089/Lucentis

Combining a single dose of IBI-20089 (6.9 mg or 13.8 mg) intravitreal injection adjunctively with Lucentis 0.5 mg intravitreal injection at baseline and monthly intravitreal Lucentis injection PRN based on clinical and OCT results.

Trial Locations (1)

60612

UIC Eye and Ear Infirmary, Chicago

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

ICON Bioscience Inc

INDUSTRY

lead

University of Illinois at Chicago

OTHER