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COMPLETED
NCT05989126
PHASE3

Study to Evaluate an 8 mg Aflibercept (EYLEA®) Prefilled Syringe (PFS)

Sponsor: Regeneron Pharmaceuticals

View on ClinicalTrials.gov

Summary

Regeneron Pharmaceuticals developed a single-dose pre-filled syringe (PFS) to deliver 8 mg aflibercept. The PFS is a convenient device that contains the study medication that will be injected in your study eye. A PFS offers a sterile, single dose of study drug within the syringe; this eliminates the need for the retina specialist to prepare the injection syringe from a separate vial. This Phase IIIb study is focused on patients with diabetic macular edema (DME) and neovascular (wet) age-related macular degeneration (nAMD). The main aim of the study is to evaluate if the 8 mg aflibercept PFS allows for successful preparation and administration of 8 mg aflibercept by retina specialists. The study will also assess the safety of 8 mg aflibercept PFS use. Regeneron will use the information from the study to better understand if the PFS can be used safely and effectively by retina specialists to administer 8 mg aflibercept.

Official title: A Study in Patients With Diabetic Macular Edema or Neovascular Age-Related Macular Degeneration to Evaluate a High Dose Aflibercept (8 mg) Prefilled Syringe

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

35

Start Date

2024-04-15

Completion Date

2024-05-31

Last Updated

2026-05-28

Healthy Volunteers

No

Interventions

DRUG

aflibercept 8 mg PFS

Sterile aqueous solution in a single-dose PFS administered by intravitreal (IVT) injection

Locations (2)

Retina Consultants of Texas

Bellaire, Texas, United States

Retina Consultants of Texas

The Woodlands, Texas, United States