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NCT07614776 · ClinicalTrials.gov registry record · Phase 3

A Study to Evaluate Efficacy, Safety, and Immunogenicity With ABP 938 8 mg Versus EYLEA® HD (Aflibercept) in Participants With Neovascular Age-related Macular Degeneration

A Phase 3 study, sponsored by Amgen.

Recruiting
Registry status
Phase 3
Development phase
304
Enrollment target

NCT07614776: Recruiting Phase 3 study, sponsored by Amgen.

NCT07614776 is a Phase 3 study that is actively recruiting participants, run by Amgen. The registered enrollment target is 304 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (61% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07614776, a Phase 3 study, is actively recruiting participants, sponsored by Amgen.

RECRUITING
Registry status
Phase 3
Development phase
304 participants
Enrollment target

Study Summary

The aim of this trial is to demonstrate similarity in efficacy between ABP 938 8 mg and aflibercept (US) 8 mg by evaluating the change in best corrected visual acuity (BCVA) in participants with neovascular age-related macular degeneration (nAMD)

Interventions

  • DRUG ABP 938 8 mg
  • DRUG Aflibercept (US) 8 mg

Trial Details

FieldValue
Enrollment Target 304 participants
Start Date 2026-05-27
Est. Completion 2028-01-12
Phase Phase 3
Amgen

558 total trials

What NCT07614776 shows while recruiting

NCT07614776 is an interventional study that assigns participants to a tested intervention. The registered 304 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (61% lower).

The record links to 0 conditions, and to 2 interventions - of which ABP 938 8 mg is the first listed.

NCT07614776 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07614776 about?

NCT07614776 is a clinical study titled "A Study to Evaluate Efficacy, Safety, and Immunogenicity With ABP 938 8 mg Versus EYLEA® HD (Aflibercept) in Participants With Neovascular Age-related Macular Degeneration". The aim of this trial is to demonstrate similarity in efficacy between ABP 938 8 mg and aflibercept (US) 8 mg by evaluating the change in best corrected visual acuity (BCVA) in participants with neovascular age-related macular degeneration (nAMD)

What is the current status of trial NCT07614776?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 304 participants. The study started on 2026-05-27. Estimated completion is 2028-01-12.

What interventions are being tested in trial NCT07614776?

The interventions under investigation include: ABP 938 8 mg (DRUG), Aflibercept (US) 8 mg (DRUG).

Who is sponsoring clinical trial NCT07614776?

This trial is sponsored by Amgen, which has 558 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT07614776's enrollment target sits among peer trials

304 1117th of 2000 higher than 882 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT07614776, the US trial registry maintained by the National Library of Medicine. NCT07614776 (mid enrollment · none site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.