The primary objective of the study is to investigate the safety of intravitreal (IVT) REGN2176-3 in patients with neovascular wet age-related macular degeneration (AMD).
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
12
Unnamed facility
Beverly Hills, California, United States
Unnamed facility
Colorado Springs, Colorado, United States
Unnamed facility
Boston, Massachusetts, United States
Unnamed facility
Houston, Texas, United States
Safety
The primary endpoint in the study is the incidence of treatment emergent adverse events (TEAEs) from day 1 through week 24 in patients treated with IVT REGN2176-3.
Time frame: day 1 through week 24
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