Safety and Efficacy of Abicipar Pegol in Participants With Neovascular Age-related Macular Degeneration

Recruiting

Trial ID: NCT02462486

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)

Stanford Investigator(s)

Theodore Leng, MD, FACS
Theodore Leng, MD, FACS

Associate Professor of Ophthalmology and, by courtesy, of Anesthesiology, Perioperative and Pain Medicine (Adult MSD)

Eligibility


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

Intervention(s):

drug: abicipar pegol

drug: ranibizumab

other: sham procedure

Recruiting

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305