ZIMURA in Combination With LUCENTIS in Patients With Neovascular Age Related Macular Degeneration (NVAMD)

Completed · Phase 2

Conditions studied: Neovascular Age-related Macular Degeneration

In brief

To assess the safety of intravitreal Zimura™ (complement factor C5 inhibitor) administered in combination with Lucentis® 0.5 mg in treatment naïve subjects with neovascular age related macular degeneration (NVAMD)

Key facts

Study ID
NCT03362190
Run by
Ophthotech Corporation
People needed
64
Starts
2017-10-11
Expected to finish
2018-10-18
Last updated by the study team
2025-06-10

Who can join

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

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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