Overview
Study EvAluating Genotypes While Using Lucentis 2
Status:
Completed
Completed
Trial end date:
2013-01-01
2013-01-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
The purpose of the study is to investigate whether the efficacy of Lucentis treatment for exudative age-related macular degeneration is associated with VEGF and HTRA1 DNA polymorphismsPhase:
Phase 4Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
University of California, San DiegoCollaborator:
Genentech, Inc.Treatments:
Ranibizumab
Criteria
Inclusion Criteria:- Ability to provide written informed consent and comply with the study assessments for
the full duration of the study.
- Age > 50 years.
- Treatment naïve (study eye only) AMD patients that are determined to be candidates for
ranbizumab.
- Visual acuity 20/32 to 20/230.
Exclusion Criteria:
- Pregnancy
- Prior enrollment in the study
- Any other condition that the investigator believes would pose a significant hazard to
the subject if the investigational therapy were initiated
- Previous therapy in study eye for AMD or other retinal disease which may be used in
the treatment of AMD.
- Any other condition that the investigator believes would pose a significant hazard to
the subject if on-label ranibizumab were prescribed
- Any participation in another simultaneous medical investigation or trial for AMD
*Concurrent eye disease in the study eye that could compromise visual acuity (e.g.,
diabetic retinopathy, advanced glaucoma)