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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)

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NCT06510816 · readout in 73 d

Sponsored by Annexon, Inc. (industry) · ANNX — their whole pipeline →.

Phase
Phase 3
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · Quadruple · Treatment
Enrollment
659actual
Sites
132
Countries
Australia, Austria, Canada +11

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2024-07-30actualWhen the study began enrolling
Primary completion2026-10-31estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2027-07-31estimatedThe whole study's end, after follow-up
First posted2024-07-19actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-05-04actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Geographic Atrophy

Interventions

  • Drug: Vonaprument — also filed as ANX007
  • Other: Sham Administration

Primary outcome

what the primary-completion date above is the date OF
Proportion of Participants Experiencing a Best Corrected Visual Acuity (BCVA) ≥15-letter Loss from Baseline Through Month 15 as Assessed by the Early Treatment Diabetic Retinopathy Study (ETDRS) Chart at Any Two Consecutive Visits
measured Baseline through Month 15

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