BENITIONSClinical Trial Intelligence

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

3期 已完成 NCT05989126

适应症Diabetic Macular Edema, Neovascular Age-Related Macular Degeneration
分期3期
申办方Regeneron Pharmaceuticals
状态已完成
受试者人数35 人
干预(药物)aflibercept 8 mg PFS
开始日期2024年4月15日
完成日期2024年5月31日
结果公布日2026年5月28日

摘要

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.

Number of 8 mg Aflibercept Injections Successfully Administered Utilizing the PFS

At Day 1 · injections

Aflibercept 8 mg PFS35 injections

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本页整理自 ClinicalTrials.gov 的公开数据,不构成医疗建议,也不构成投资建议。请务必咨询专业医师。