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A Study About the Safety of ASP3021 Eye Injections and if They Help People in Japan With Vision Loss From Age-related Macular Degeneration

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NCT06970665 · readout in 315 d

Sponsored by Astellas Pharma Inc (industry) · 4503.T — their whole pipeline →.

Phase
Phase 4
Status
Active, not recruiting
Study type
Interventional
Design
Na · None · Treatment
Enrollment
17actual
Sites
16
Country
Japan

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
Start2025-07-08actualWhen the study began enrolling
Primary completion2027-06-30estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2027-06-30estimatedThe whole study's end, after follow-up
First posted2025-05-14actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-12actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Geographic Atrophy
  • Age-Related Macular Degeneration

Intervention

  • Drug: avacincaptad pegol — also filed as ASP3021, IZERVAY

Primary outcomes

what the primary-completion date above is the date OF
Number of participants with Treatment Emergent Adverse Events (TEAEs)
measured Up to 12 Months
Number of participants with Serious TEAEs
measured Up to 12 Months

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