# Annexon, Inc.: Phase 3 study closed enrollment, 659 enrolled (Geographic Atrophy)

**Score:** 75/100

| Field | Value |
|---|---|
| Sponsor | Annexon, Inc. |
| Sponsor type | Industry (pharma, biotech, medtech) |
| Study | A Study Investigating the Efficacy and Safety of Intravitreal (IVT) Injections of Vonaprument (Formerly ANX007) in Participants With Dry Age-Related Macular Degeneration (AMD) With Geographic Atrophy (GA) |
| NCT ID | NCT06510816 |
| Phase | Phase 3 |
| Status | active not recruiting |
| Conditions | Geographic Atrophy |
| Intervention types | drug, other |
| Target enrollment | 659 |
| Site countries | United States, Australia, Austria, Canada, Czechia, France, Germany, Hungary, Italy, Netherlands, New Zealand, Poland |
| Posted | 2024-07-19 |
| Planned start | 2024-07-30 |
| Event | Enrollment closed (active, not recruiting) |
| Event date | 2026-10-06 |
| Last update posted | 2026-10-06 |

## Why this score
- Industry sponsor (buys outsourced services).
- Enrollment closed: data management, monitoring and closeout ahead.
- Phase 3: multi-site, larger budget.
- 659 participants planned.

Source: ClinicalTrials.gov (U.S. National Library of Medicine) API v2 (https://clinicaltrials.gov/study/NCT06510816). Last refreshed: 2026-11-04T06:04:38.232Z.
From public ClinicalTrials.gov registrations. Sponsor and study level only: we never list investigators, contacts or participants. A registration describes a planned study and can change. Status changes are read from each study's current status, actual dates and latest posted update, not a full change history, so an update can be a correction rather than a new change. Verify on ClinicalTrials.gov.