Safety and Efficacy of Abicipar Pegol in Participants With Neovascular Age-related Macular Degeneration
Trial ID or NCT#
NCT02462486
Status
NOT RECRUITING
Purpose
This is a safety and efficacy study of abicipar pegol in participants with neovascular age-related macular degeneration.
Official Title
Safety and Efficacy of Abicipar Pegol (AGN-150998) in Patients With Neovascular Age-related Macular Degeneration (SEQUOIA Study)
Eligibility Criteria
Ages Eligible for Study: Older than 50 Years
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers: Yes
Inclusion Criteria:
- * Diagnosis of age-related macular degeneration in at least 1 eye* Best corrected visual acuity of 20/40 to 20/320 in the study eye* Best corrected visual acuity of 20/200 or better in the non-study eye
Exclusion Criteria:
- * History of vitrectomy, macular surgery, or glaucoma surgery in the study eye* Cataract or refractive surgery in the study eye within the last 3 months
Investigator(s)
Theodore Leng, MD, FACS
Ophthalmologist
Professor of Ophthalmology (Ophthalmology Research/Clinical Trials) and, by courtesy, of Anesthesiology, Perioperative and Pain Medicine (MSD)
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