Ireland
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Active, not recruiting Phase 2

Study to Assess the Efficacy & Safety of KHK4951 in Patients With Diabetic Macular Edema

NCT06116916 · tracked via the Priya Life Science Australia tracker
Phase
Phase 2
Started
2024-01-09
Last updated
2025-10-30

Condition(s) studied

Diabetic Macular Edema (DME)

Investigational drug(s) / intervention(s)

KHK4951 →Aflibercept Injection →

KHK4951: KHK4951 eye drop for 36 weeks until end of the trial

Aflibercept Injection: Intravitreal injection (IVT) of aflibercept will be given as specified in the protocol

Study summary

The purpose of this study is to evaluate efficacy and safety of KHK4951 eye drops in patients with DME.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Voluntary written informed consent to participate in the study * In Korea, participants must be 19 years or older to be enrolled * BCVA ETDRS letter score of 78 letters to 35 letters as measured by the ETDRS visual acuity chart in the study eye at screening * 500 μm ≥ CST ≥ 325 μm in the study eye at screening * HbA1c ≤ 11% at screening Exclusion Criteria: * Any signs of proliferative diabetic retinopathy in the study eye * History of rubeosis in the study eye * Uncontrolled glaucoma in the study eye * Aphakia or pseudophakia with AC-IOL in the study eye * Active intraocular inflammation in the study eye * Any current ocular condition for which visual acuity loss would not improve from resolution of macular edema in the study eye * History of rhegmatogenous retinal detachment in the study eye * Any current or history of ocular disease other than DME that may confound assessment of the macula or affect central vision in the study eye * History of the following therapies in the study eye * History of vitrectomy surgery, submacular surgery, or other surgical intervention for DME * Periocular or intraocular (sub-Tenon or IVT) corticosteroids within 12 weeks prior to Day 1 corticosteroids * Previous intraocular device implantation except PC-IOL * Laser (any type) to the macular area within 12 weeks prior to Day 1 * Peripheral retinal photocoagulation therapy within 12 weeks prior to Day 1 * Previous treatment with IVT anti-VEGF drugs other than ranibizumab, bevacizumab, aflibercept 2 mg, and their biosimilars * Treatment with ranibizumab, bevacizumab, aflibercept 2 mg, or their biosimilars within 12 weeks prior to Day 1. Previously treated patients who received these medications more than 12 weeks prior to Day 1 can be enrolled, but the patients should be diagnosed with DME within 3 years prior to Day 1 * Previous use of Ozurdex® or Iluvien® implant * Any current or history of endophthalmitis in either eye * History of idiopathic or autoimmune-associated uveitis in either eye * Active infectious conjunctivitis, keratitis, scleritis, or endophthalmitis in either eye

Primary outcome measure(s)

  • Reduction of 15 or more letters in BCVA (Best corrected visual acuity) as measured by ETDRS visual acuity chart from baseline — For 36 weeks until the end of the trial

Trial sites (87)

FacilityCityRegionStatus
Barnet Dulaney Perkins Eye Center - Phoenix Mesa Arizona
Retina Associates Southwest, P.C. Tucson Arizona
Win Retina Arcadia California
Retina Vitreous Associates Medical Group Beverly Hills California
The Retina Partners Encino California
Salehi Retina Institute, Inc Huntington Beach California
California Eye Specialists Medical Group Inc Pasadena California
Retina Consultants of Southern California Redlands California
Retina Consultants of Southern CO Colorado Springs Colorado
Blue Ocean Clinical Research West Clearwater Florida
Florida Eye Associates Melbourne Florida
Eye Associates of Pinellas Pinellas Park Florida
Ft. Lauderdale Eye Institute Plantation Florida
Retina Vitreous Associates of Florida - Saint Petersburg St. Petersburg Florida
Southern Vitreoretinal Associates Tallahassee Florida
Center for Retina and Macular Disease - Ophthalmology Winter Haven Florida
Mid Atlantic Retina Specialists - Hagerstown Hagerstown Maryland
Sierra Eye Associates Reno Nevada
Envision Ocular, LLC Bloomfield New Jersey
Vision Research Center Eye Associates of New Mexico Albuquerque New Mexico
Retina Vitreous Surgeons of Central NY, PC Liverpool New York
Ophthalmic Consultants of Long Island Oceanside New York
Retina Vitreous Center in Edmond Oklahoma Edmond Oklahoma
EyeHealth Northwest Portland Oregon
Wills Eye Health System Bethlehem Pennsylvania
Eye Care Specialists Kingston Pennsylvania
Retina Consultants of Charleston - (RCA Network Site) Charleston South Carolina
Charleston Neuroscience Institute (RCA Network Site) Ladson South Carolina
Black Hills Regional Eye Institute - Ophthalmology Rapid City South Dakota
Charles Retina Institute Germantown Tennessee
Retina Research Institute of Texas Abilene Texas
Austin Retina Associates - Ophthalmology/Retina (RCA Network site) Austin Texas
Austin Clinical Research, LLC Austin Texas
Retina Consultants of Texas Bellaire Texas
Texas Retina Associates Fort Worth Texas
Retinal Consultants of Texas- San Antonio (RCA Network site) San Antonio Texas
Retina Consultants of Texas (RCA Network Site) The Woodlands Texas
Strategic Clinical Research Group, LLC Willow Park Texas
University of Vermont Fletcher Allen Health Care Burlington Vermont
Retina Group of Washington Fairfax Virginia

+ 47 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 NCT06116916 on ClinicalTrials.gov ↗ ← All trials in Australia