Ireland
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Recruiting Phase 3

A Phase 3 Trial for Intravitreal Injection of 4D-150 in Adults With Diabetic Macular Edema (DME).

NCT07867080 · tracked via the Priya Life Science Japan tracker
Phase
Phase 3
Started
2026-09-18
Last updated
2026-10-13

Condition(s) studied

Diabetic Macular Edema (DME)

Investigational drug(s) / intervention(s)

4D-150 IVT (3x10^10 vg) →EYELEA ® (aflibercept) Injection 2 mg (0.05mL)

4D-150 IVT (3x10^10 vg): If randomized to the 4D-150 treatment arm, 4D-150 will be administered at the assigned dose level as a single dose IVT injection on Day 1

EYELEA ® (aflibercept) Injection 2 mg (0.05mL): EYLEA ® (aflibercept) will be administered at applicable visits

Study summary

A Phase 3, Randomized, Double-Masked, Active-Controlled Trial to Evaluate the Safety, Efficacy, and Durability of a Single Intravitreal Injection of 4D-150 versus Aflibercept in Adults with Diabetic Macular Edema (4SIGHT)

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
5.2 Inclusion Criteria Individuals eligible to participate in the trial must meet the following inclusion criteria: General Inclusion Criteria 1. Signed informed consent before any protocol-specified assessment is performed 2. Ability and willingness to comply with the protocol-specified procedures (including IVT injection) and visits, in the Investigator's judgment 3. ≥18 years of age at time of signing informed consent 4. Documented diagnosis of diabetes mellitus (Type 1 or Type 2) 5. WOCBP must agree to use highly effective contraception from the time of informed consent, through duration of trial participation 6. Agree to use a barrier method (e.g., condom) during intercourse for 3 months after Day 1 to prevent fluid transmission; sexually active males should not father a child or donate sperm during this period Ocular Inclusion Criteria 7. Macular thickening secondary to DME involving the center of the fovea (confirmed by the Reading Center) in the study eye 8. Study eye amenable to IVT injection identified 9. Presence of intraretinal fluid and/or subretinal fluid secondary to DME 10. Decreased visual acuity attributable primarily to DME, as determined by the Investigator 11. Demonstrated clinical response to aflibercept and functional stability in the study eye Exclusion Criteria: Individuals who meet any of the following exclusion criteria will not be eligible to participate: Ocular Condition 1. Macular conditions other than DME 2. History or presence of moderate Proliferative Diabetic Retinopathy or worse 3. History of retinal detachment in the study eye 4. History or presence of active inflammation or infection in either eye 5. History or presence of low Intraocular Pressure 6. Uncontrolled glaucoma or intraocular hypertension Ocular Treatments/Interventions: 7. Any prior concomitant treatment for DME 8. History of prior significant ocular surgery or treatment 9. Any prior investigational drug, agent, device, or gene therapy

Primary outcome measure(s)

  • Mean change from baseline in Early Treatment Diabetic Retinopathy Study best-corrected visual acuity letter score at Week 52 — 52 weeks
    The minimum and maximum values are: 0 to 100 The higher the value the better the result

Trial sites (82)

FacilityCityRegionStatus
Research Network Arizona Scottsdale Arizona Recruiting
The Retina Partners Encino California Recruiting
Retina Consultants of Orange County Fullerton California Not Yet Recruiting
Retinal Consultants Medical Group Inc. Sacramento California Not Yet Recruiting
Retina Consultants San Diego San Diego California Not Yet Recruiting
Retina Institute of New England San Mateo California Not Yet Recruiting
Bay Area Retina Associates - Walnut Creek Walnut Creek California Not Yet Recruiting
Retina Specialists of Colorado - Aurora Aurora Colorado Recruiting
Retina Consultants of Southern Colorado P.C. Colorado Springs Colorado Not Yet Recruiting
Southwest Retina Consultants Durango Colorado Not Yet Recruiting
Coastal Eye- Greenwich Greenwich Connecticut Not Yet Recruiting
Retina Institute of New England, PC Waterford Connecticut Not Yet Recruiting
Florida Retina Institute Orlando Florida Not Yet Recruiting
Retinal Specialty Institute Pensacola Florida Recruiting
Fort Lauderdale Eye Institute (FLEI)-Plantation Plantation Florida Not Yet Recruiting
Retina Vitreous Associates of Florida Tampa Florida Recruiting
Retina Associates, Ltd. Elmhurst Illinois Recruiting
University Retina and Macula Associates Oak Forest Illinois Not Yet Recruiting
Illinois Retina Associates Oak Park Illinois Not Yet Recruiting
Springfield Clinic Springfield Illinois Not Yet Recruiting
Midwest Eye Institute Carmel Indiana Not Yet Recruiting
The Retina Group of Washington Chevy Chase Maryland Not Yet Recruiting
Cumberland Valley Retina Consultants Hagerstown Maryland Not Yet Recruiting
Mid Atlantic Retina Specialist Hagerstown Maryland Not Yet Recruiting
Mississippi Retina Associates Madison Mississippi Not Yet Recruiting
Deep Blue Retina Clinical Research, PLLC Southaven Mississippi Not Yet Recruiting
The Retina Institute St Louis Missouri Not Yet Recruiting
Sierra Eye Associates Reno Nevada Recruiting
Envision Ocular, LLC Bloomfield New Jersey Not Yet Recruiting
NJ Retina Edison New Jersey Not Yet Recruiting
NYU Langone Health New York New York Not Yet Recruiting
Retina Vitreous Surgeons of CNY, PC New York New York Not Yet Recruiting
Vitreoretinal Consultants of New York (VRCNY) Westbury New York Not Yet Recruiting
Asheville Eye Associates - Retina Division Asheville North Carolina Not Yet Recruiting
North Carolina Retina Associates- Wake Forest Wake Forest North Carolina Not Yet Recruiting
Retina Vitreous Center Edmund Oklahoma Not Yet Recruiting
EyeHealth Northwest Portland Oregon Not Yet Recruiting
Mid Atlantic Retina Bethlehem Pennsylvania Not Yet Recruiting
Black Hills Regional Eye Institute Rapid City South Dakota Not Yet Recruiting
West Texas Retina Consultants Abilene Texas Not Yet Recruiting

+ 42 more sites — see the full list on the official registry below.

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07867080 on ClinicalTrials.gov ↗ ← All trials in Japan