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Clinical Trial Summary

This study will evaluate the effectiveness and safety of a 36-week refill regimen for the Port Delivery System with ranibizumab 100 mg/mL (PDS Q36W) compared with intravitreal injections of aflibercept (2 mg) administered per treat-and-extend (aflibercept T&E) in subjects with neovascular (wet) age-related macular degeneration (nAMD).

Clinical Trial Description


Study Design

Related Conditions & MeSH terms

NCT number NCT05126966
Study type Interventional
Source Hoffmann-La Roche
Contact Reference Study ID Number: MR42410
Phone 888-662-6728 (U.S. and Canada)
Email [email protected]
Status Not yet recruiting
Phase Phase 3
Start date March 24, 2022
Completion date March 25, 2025

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