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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
NCT06556368 · View on ClinicalTrials.gov ↗
Study Summary
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)
Conditions Studied
Interventions
- DRUG Aflibercept
- DRUG Tarcocimab tedromer
- DRUG Tabirafusp tedromer
Study Locations (20)
California
- Retina Consultants of Orange County — Fullerton
- Global Research Management, Inc. - Lugene Eye Institute — Glendale
- Retinal Consultants Medical Group, Inc. — Modesto
- California Eye Specialists Medical Group, Inc. — Pasadena
- California Eye Specialists Medical Group, Inc. — Redlands
- Retinal Consultants Medical Group Inc — Sacramento
Florida
- Blue Ocean Clinical Research — Clearwater
- Retina Group of Florida — Fort Lauderdale
- National Ophthalmic Research Institute — Fort Myers
- Retina Group of Florida — Sarasota
- Center for Retina and Macular Disease — Winter Haven
Arizona
- Associated Retina Consultants — Gilbert
- Associated Retina Consultants — Phoenix
- Retina Macula Institute of Arizona — Scottsdale
- Retina Associates SW — Tucson
Illinois
- Retina Associates, Ltd — Elmhurst
- Illinois Retina Associates — Oak Park
Colorado
- Retina Consultants of Southern Colorado — Colorado Springs
Connecticut
- Retina Group of New England, PC — Waterford
Georgia
- Southeast Retina Center — Augusta
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 675 participants |
| Start Date | 2024-08-23 |
| Est. Completion | 2027-08 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06556368
The ClinicalTrials.gov registry entry for NCT06556368 describes a study currently listed as active not recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 675 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Kodiak Sciences, which has 5 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Wet Age-related Macular Degeneration appearing as the primary indexed condition, and to 3 interventions — of which Aflibercept is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06556368 reports 20 study locations spanning 7 distinct geographic areas — top geographies include California, Florida, Arizona. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06556368 about?
NCT06556368 is a clinical study titled "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". 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)
What is the current status of trial NCT06556368?
This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 675 participants. The study started on 2024-08-23. Estimated completion is 2027-08.
What conditions does trial NCT06556368 study?
This clinical trial studies the following conditions: Wet Age-related Macular Degeneration. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06556368?
The interventions under investigation include: Aflibercept (DRUG), Tarcocimab tedromer (DRUG), Tabirafusp tedromer (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06556368?
This trial is sponsored by Kodiak Sciences, which has 5 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06556368 being conducted?
This trial has 20 study locations across Arizona, California, Colorado, Connecticut, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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