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A Study to Evaluate the Efficacy and Safety of Tarcocimab Tedromer and Tabirafusp Tedromer Compared to Aflibercept in Participants With Neovascular (Wet) Age-related Macular Degeneration (wAMD) - DAYBREAK

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NCT06556368 · readout ≤ 12 d

Sponsored by Kodiak Sciences Inc (industry) · KOD — their whole pipeline →.

Phase
Phase 3
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · Quadruple · Treatment
Enrollment
675estimated
Sites
72
Countries
Puerto Rico, United States

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
Start2024-08-23actualWhen the study began enrolling
Primary completionAug 2026estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionAug 2027estimatedThe whole study's end, after follow-up
First posted2024-08-16actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-04-29actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Wet Age-related Macular Degeneration

Interventions

  • Drug: Tarcocimab tedromer — also filed as KSI-301
  • Drug: Tabirafusp tedromer — also filed as KSI-501
  • Drug: Aflibercept — also filed as Eylea

Primary outcome

what the primary-completion date above is the date OF
Best corrected visual acuity (BCVA)
measured Week 48

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