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NCT04270747 · ClinicalTrials.gov registry record · Phase 3

A Study to Understand Effectiveness and Safety of ABP 938 Compared to Aflibercept (Eylea®) in Patients Suffering With Neovascular Age-related Macular Degeneration [Neovascular (Wet) AMD]

A Phase 3 study, sponsored by Amgen.

Completed
Registry status
Phase 3
Development phase
576
Enrollment target

NCT04270747 is a Phase 3 study that has completed, run by Amgen. The registered enrollment target is 576 participants.

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The verdict

NCT04270747, a Phase 3 study, has completed, sponsored by Amgen.

COMPLETED
Registry status
Phase 3
Development phase
576 participants
Enrollment target

Study Summary

The purpose of this study is to compare the efficacy and safety of ABP 938 versus Aflibercept (Eylea®) in the treatment of neovascular age-related macular degeneration. Subjects will be randomized in a masked 1:1 ratio to receive 2 mg (0.05 mL) of either ABP 938 (Treatment Group A) or aflibercept (Treatment Group B) administered by intravitreal (IVT) injection.

Interventions

  • DRUG Aflibercept
  • DRUG ABP 938

Trial Details

FieldValue
Enrollment Target 576 participants
Start Date 2020-06-22
Est. Completion 2023-01-30
Phase Phase 3

Sponsor

Amgen

558 total trials

What the Registry Record Tells You About NCT04270747

The ClinicalTrials.gov registry entry for NCT04270747 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 576 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Amgen, which has 558 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Aflibercept is the first listed.

NCT04270747 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT04270747 about?

NCT04270747 is a clinical study titled "A Study to Understand Effectiveness and Safety of ABP 938 Compared to Aflibercept (Eylea®) in Patients Suffering With Neovascular Age-related Macular Degeneration [Neovascular (Wet) AMD]". The purpose of this study is to compare the efficacy and safety of ABP 938 versus Aflibercept (Eylea®) in the treatment of neovascular age-related macular degeneration. Subjects will be randomized in a masked 1:1 ratio to receive 2 mg (0.05 mL) of either ABP 938 (Treatment Group A) or aflibercept (T...

What is the current status of trial NCT04270747?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 576 participants. The study started on 2020-06-22. Estimated completion is 2023-01-30.

What interventions are being tested in trial NCT04270747?

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

Who is sponsoring clinical trial NCT04270747?

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

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.