Regeneron CAPELLA

Status: Closed

ClinicalTrials.gov Identifier: NCT02418754

Regeneron CAPELLA R2176-3AMD-1417: A Phase 2, Double-masked, Randomized, Controlled, Multiple-dose, Regimen-Ranging Study of the Efficacy and Safety of Intravitreal REGN2176-3 in Patients with Neovascular Age-related Macular Degeneration

Condition: Neovascular AMD

Study Type: Interventional

Duration: 52 weeks

Eligibility:

Ages: 50 years and older
Sexes: All
Accepts Healthy Volunteers: No

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