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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

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05126966
Study type Interventional
Source Hoffmann-La Roche
Contact
Status Withdrawn
Phase Phase 3
Start date December 29, 2023
Completion date January 30, 2026

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