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NCT01969708 · ClinicalTrials.gov registry record · Phase 3

Study of Comparative Treatments for Retinal Vein Occlusion 2 (SCORE2)

A Phase 3 study, sponsored by The Emmes Company.

Completed
Registry status
Phase 3
Development phase
362
Enrollment target

NCT01969708 is a Phase 3 study that has completed, run by The Emmes Company. The registered enrollment target is 362 participants.

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The verdict

NCT01969708, a Phase 3 study, has completed, sponsored by The Emmes Company.

COMPLETED
Registry status
Phase 3
Development phase
362 participants
Enrollment target

Study Summary

SCORE2 is a multicenter, prospective, randomized, phase III clinical trial in which all participants enrolled will be followed for up to 2.5 years. SCORE2 is designed as a non-inferiority trial, with study eyes randomized to intravitreal bevacizumab (1.25 mg) every 4 weeks vs. intravitreal aflibercept (2.0 mg) every 4 weeks. SCORE2 aims to determine if bevacizumab is non-inferior to aflibercept for the treatment of macular edema associated with central retinal vein occlusion (CRVO), with the primary outcome of visual acuity measured at Month 6.

Interventions

  • DRUG bevacizumab
  • DRUG aflibercept

Trial Details

FieldValue
Enrollment Target 362 participants
Start Date 2014-09
Est. Completion 2021-03
Phase Phase 3

Sponsor

The Emmes Company

11 total trials

What the Registry Record Tells You About NCT01969708

The ClinicalTrials.gov registry entry for NCT01969708 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 362 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is The Emmes Company, which has 11 total studies on file at ClinicalTrials.gov.

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

NCT01969708 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01969708 about?

NCT01969708 is a clinical study titled "Study of Comparative Treatments for Retinal Vein Occlusion 2 (SCORE2)". SCORE2 is a multicenter, prospective, randomized, phase III clinical trial in which all participants enrolled will be followed for up to 2.5 years. SCORE2 is designed as a non-inferiority trial, with study eyes randomized to intravitreal bevacizumab (1.25 mg) every 4 weeks vs. intravitreal afliberce...

What is the current status of trial NCT01969708?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 362 participants. The study started on 2014-09. Estimated completion is 2021-03.

What interventions are being tested in trial NCT01969708?

The interventions under investigation include: bevacizumab (DRUG), aflibercept (DRUG).

Who is sponsoring clinical trial NCT01969708?

This trial is sponsored by The Emmes Company, which has 11 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.