Study of a High-Dose Aflibercept in Participants With Diabetic Eye Disease

Trial ID or NCT#

NCT04429503

Status

not recruiting iconNOT RECRUITING

Purpose

The primary objective of the study is to determine if treatment with high-dose aflibercept (HD) at intervals of 12 or 16 weeks provides non-inferior best corrected visual acuity (BCVA) compared to aflibercept dosed every 8 weeks. The secondary objectives of the study are as follows: * To determine the effect of HD vs. aflibercept on anatomic and other visual measures of response * To evaluate the safety, immunogenicity, and pharmacokinetics (PK) of aflibercept

Official Title

A Randomized, Double-Masked, Active-Controlled Phase 2/3 Study of the Efficacy and Safety of High-Dose Aflibercept in Patients With Diabetic Macular Edema

Eligibility Criteria

Ages Eligible for Study: Older than 18 Years
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers: No
Inclusion Criteria:
  1. * Diabetic macular edema (DME) with central involvement in the study eye* Best corrected visual acuity (BCVA) early treatment diabetic retinopathy study (ETDRS) letter score of 78 to 24 (approximate Snellen equivalent of 20/32 to 20/320) in the study eye with decreased vision determined to be primarily the result of DME* Willing and able to comply with clinic visits and study-related procedures* Provide informed consent signed by study participant or legally acceptable representative
    1. Extension Phase: All randomized patients that complete visit 26, week 96, as long as the patient 1) provides informed consent and 2) no treatment for DME has been given in the study eye other than the randomized study treatment.
    2. Key
Exclusion Criteria:
  1. * Evidence of macular edema due to any cause other than diabetes mellitus in either eye* Active proliferative diabetic retinopathy in the study eye* IVT anti-VEGF treatment (aflibercept, ranibizumab, bevacizumab, brolucizumab, pegaptanib sodium) or panretinal laser photocoagulation (PRP) /macular laser photocoagulation within 12 weeks (84 days) or intraocular or periocular corticosteroids within 16 weeks (112 days) of the screening visit in the study eye* Prior IVT investigational agents in either eye (eg, anti-ang-2/anti-VEGF bispecific monoclonal antibodies, gene therapy, etc.) at any time* Treatment with ocriplasmin (JETREA®) in the study eye at any time
    • NOTE: Other Protocol Defined Inclusion/Exclusion Criteria Apply
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Investigator(s)

Diana Do, MD
Diana Do, MD
Retina specialist, Ophthalmologist
Professor of Ophthalmology

View on ClinicalTrials.gov