Clinical trial

A Phase 3 Safety and Efficacy Study of Intravitreal Administration of Zimura…

NCT04435366 · IVERIC bio, Inc., Industry · Completed

Key facts

NCT number NCT04435366
Title A Phase 3 Safety and Efficacy Study of Intravitreal Administration of Zimura (Complement C5 Inhibitor)
Official title A Phase 3 Multicenter, Randomized, Double Masked, Sham- Controlled Clinical Trial to Assess the Safety and Efficacy of Intravitreal Administration of Zimura (Complement C5 Inhibitor) in Patients With Geographic Atrophy Secondary to Age-Related Macular Degeneration
Lead sponsor IVERIC bio, Inc., Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Geographic Atrophy, Macular Degeneration
Intervention type Drug
Interventions Avacincaptad Pegol, Sham
Enrollment 448
Start date Jun 22, 2020
Primary completion Jul 25, 2022
Completion Aug 22, 2023
First posted Jun 17, 2020
Last update posted Oct 21, 2025
Countries Argentina, Australia, Austria, Belgium, Brazil, Canada, Colombia, Croatia, Czechia, Estonia, France, Germany and 8 more

At a glance

  • 100–999 Study sites
  • Yes Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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