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Study of a High-Dose Aflibercept in Participants With Diabetic Eye Disease
Not Recruiting
Trial ID: NCT04429503
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
Stanford Investigator(s)
Diana Do, MD
Professor of Ophthalmology
Eligibility
Key Inclusion Criteria:
- 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
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.
Key Exclusion Criteria:
- 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
Intervention(s):
drug: aflibercept
drug: High-dose aflibercept
Not Recruiting
Contact Information
Stanford University
School of Medicine
300 Pasteur Drive
Stanford,
CA
94305