Randomized, Single-Masked, Long-Term, Safety and Tolerability Study of VEGF Trap-Eye in AMD

Completed · Phase 2

Conditions studied: Macular Degeneration

In brief

Rollover study for subjects in prior VEGF Trap-Eye Phase I and II studies. Primary objective is to assess long-term safety and tolerability of continuing intravitreal treatment in subjects with wet age-related macular degeneration.

Key facts

Study ID

NCT00527423

Run by

Regeneron Pharmaceuticals

People needed

157

Starts

2007-08-01

Expected to finish

2011-10-01

Last updated by the study team

2013-06-12

Who can join

Age: 50 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Prior participation in VEGF Trap-Eye Phase I and II studies

You may not qualify if…

• Any ocular or systemic adverse events that would preclude participation
• Presence of any condition that would jeopardize subject's participation

Where it is running

• Study site — Peoria, Arizona, United States
• Study site — Phoenix, Arizona, United States
• Study site — Tucson, Arizona, United States
• Study site — Beverly Hills, California, United States
• Study site — Loma Linda, California, United States
• Study site — Palm Springs, California, United States
• Study site — Pasadena, California, United States
• Study site — Poway, California, United States
• Study site — Westlake Village, California, United States
• Study site — Fort Myers, Florida, United States
• Study site — Stuart, Florida, United States
• Study site — Winter Haven, Florida, United States
• Study site — Augusta, Georgia, United States
• Study site — Glenview, Illinois, United States
• Study site — Indianapolis, Indiana, United States
• Study site — Baltimore, Maryland, United States
• Study site — Hagerstown, Maryland, United States
• Study site — Boston, Massachusetts, United States
• Study site — West Springfield, Massachusetts, United States
• Study site — Toms River, New Jersey, United States
• Study site — Lynbrook, New York, United States
• Study site — Charlotte, North Carolina, United States
• Study site — Oklahoma City, Oklahoma, United States
• Study site — Portland, Oregon, United States
• Study site — West Columbia, South Carolina, United States

Full record on ClinicalTrials.gov

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