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NCT07118670 · ClinicalTrials.gov registry record · Phase 4

High Dose Eylea for Proliferative Diabetic Retinopathy Outcomes

A Phase 4 study of Proliferative Diabetic Retinopathy (PDR), sponsored by Edward Wood, MD.

Active
Registry status
Phase 4
Development phase
40
Enrollment target
3
Study locations

NCT07118670 is a Phase 4 study of Proliferative Diabetic Retinopathy (PDR) that is active but no longer recruiting, run by Edward Wood, MD. The registered enrollment target is 40 participants. The trial reports 3 study locations across 1 state.

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The verdict

NCT07118670, a Phase 4 study of Proliferative Diabetic Retinopathy (PDR), is active but no longer recruiting, sponsored by Edward Wood, MD.

ACTIVE NOT RECRUITING
Registry status
Phase 4
Development phase
40 participants
Enrollment target
3
Study locations

Study Summary

The purpose of this Phase 4 study is to evaluate the safety of aflibercept 8mg in patients with proliferative diabetic retinopathy without center-involved diabetic macular edema.

Interventions

  • DRUG Aflibercept 8mg

Study Locations (3)

Texas

  • Retina Consultants of Texas - Austin Retina Associates - Austin
  • Retina Consultants of Texas - Bellaire
  • Retina Consultants of Texas - San Antonio - San Antonio

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2025-12-08
Est. Completion 2028-04
Phase Phase 4

Sponsor

Edward Wood, MD

1 total trials

What the Registry Record Tells You About NCT07118670

The ClinicalTrials.gov registry entry for NCT07118670 describes a study currently listed as active not recruiting, categorized as Phase 4. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Edward Wood, MD, which has 1 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Proliferative Diabetic Retinopathy (PDR) appearing as the primary indexed condition, and to 1 intervention - of which Aflibercept 8mg is the first listed.

NCT07118670 reports 3 study locations spanning 1 distinct geographic area - top geographies include Texas.

Frequently Asked Questions

What is clinical trial NCT07118670 about?

NCT07118670 is a clinical study titled "High Dose Eylea for Proliferative Diabetic Retinopathy Outcomes". The purpose of this Phase 4 study is to evaluate the safety of aflibercept 8mg in patients with proliferative diabetic retinopathy without center-involved diabetic macular edema.

What is the current status of trial NCT07118670?

This trial is currently active not recruiting. It is a Phase 4 study. The enrollment target is 40 participants. The study started on 2025-12-08. Estimated completion is 2028-04.

What conditions does trial NCT07118670 study?

This clinical trial studies the following conditions: Proliferative Diabetic Retinopathy (PDR).

What interventions are being tested in trial NCT07118670?

The interventions under investigation include: Aflibercept 8mg (DRUG).

Who is sponsoring clinical trial NCT07118670?

This trial is sponsored by Edward Wood, MD, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07118670 being conducted?

This trial has 3 study locations across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

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