Study to Assess the Efficacy & Safety of KHK4951 in Patients With Neovascular Age-Related Macular Degeneration
A Phase 2, Multicenter, Randomized, Double-Masked, Parallel Group Study to Assess the Efficacy and Safety of KHK4951, a Vascular Endothelial Growth Factor Receptor Inhibitor, in Patients With Neovascular Age-Related Macular Degeneration
1 other identifier
interventional
180
4 countries
84
Brief Summary
The purpose of this study is to evaluate efficacy and safety of KHK4951 eye drops in patients with nAMD.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for phase_2
Started Jan 2024
84 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
October 31, 2023
CompletedFirst Posted
Study publicly available on registry
November 3, 2023
CompletedStudy Start
First participant enrolled
January 31, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 31, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
September 30, 2026
October 30, 2025
October 1, 2025
2.6 years
October 31, 2023
October 29, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Reduction of 15 or more letters in BCVA (Best corrected visual acuity) as measured by ETDRS visual acuity chart from baseline
For 44 weeks until the end of the trial
Secondary Outcomes (4)
The number of aflibercept IVT
For 44 weeks until the end of the trial
Change from baseline in SHRM as measured by SD-OCT
44 weeks
Change from baseline in retinal morphology as measured by SD-OCT
44 weeks
Change from baseline in MNV lesion area and total MNV leakage area as measured by FA
44 Weeks
Other Outcomes (2)
Number of participants with adverse events
For 44 weeks until the end of the trial
Serum KHK4951 concentration
44 Weeks
Study Arms (3)
Arm A
EXPERIMENTALKHK4951 High dose
Arm B
EXPERIMENTALKHK4951 Middle dose
Arm C
EXPERIMENTALKHK4951 Low dose
Interventions
Intravitreal injection (IVT) of aflibercept will be given as specified in the protocol
Eligibility Criteria
You may qualify if:
- Voluntary written informed consent to participate in the study
- Active subfoveal MNV (any subtype) or juxtafoveal/extrafoveal MNV secondary to AMD with a subfoveal component related to the MNV activity in the study eye as assessed by FA (evidence of leakage) or SD-OCT (presence of fluid) judged by the central reading center at screening
- BCVA ETDRS letter score of 78 letters to 35 letters in the study eye as measured by the ETDRS visual acuity chart at screening
- CST ≥ 450 μm at screening
You may not qualify if:
- Subretinal hemorrhage, fibrosis, or atrophy of \> 50% of the total lesion area and/or that involves the fovea 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 nAMD in the study eye that may confound assessment of the macula or affect central vision
- History of the following therapies in the study eye:
- History of vitrectomy surgery, submacular surgery, or other surgical intervention for AMD
- Prior treatment PDT with Visudyne®, external-beam radiation therapy, transpupillary thermotherapy, or panretinal photocoagulation
- Periocular or intraocular (sub-Tenon or IVT) corticosteroids within 12 weeks prior to Day 1
- Previous intraocular device implantation except PC-IOL
- Previous laser (any type) to the macular area
- 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 nAMD within 3 years prior to Day 1
- +3 more criteria
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (84)
Barnet Dulaney Perkins Eye Center - Phoenix
Mesa, Arizona, 85206, United States
Retina Associates Southwest, P.C.
Tucson, Arizona, 85710, United States
Win Retina
Arcadia, California, 91006, United States
Retina Vitreous Associates Medical Group
Beverly Hills, California, 90211, United States
The Retina Partners
Encino, California, 91436, United States
Salehi Retina Institute, Inc
Huntington Beach, California, 92647, United States
Payam Amini
Pasadena, California, 91107, United States
Retina Consultants of Southern CO
Colorado Springs, Colorado, 80909, United States
Blue Ocean Clinical Research West
Clearwater, Florida, 33761, United States
Florida Eye Associates
Melbourne, Florida, 32901, United States
Eye Associates of Pinellas
Pinellas Park, Florida, 33782, United States
Ft. Lauderdale Eye Institute
Plantation, Florida, 33324, United States
Retina Vitreous Associates of Florida - Saint Petersburg
St. Petersburg, Florida, 33711, United States
Southern Vitreoretinal Associates
Tallahassee, Florida, 32308, United States
Center for Retina and Macular Disease - Ophthalmology
Winter Haven, Florida, 33880, United States
Southeast Retina Center
Augusta, Georgia, 30909, United States
Massachusetts Eye and Ear
Boston, Massachusetts, 02114, United States
Associated Retinal Consultants (ARC) P.C. - Opthalmology
Royal Oak, Michigan, 48073, United States
Sierra Eye Associates
Reno, Nevada, 89502, United States
Retina Center of New Jersey
Bloomfield, New Jersey, 07003, United States
Vision Research Center Eye Associates of New Mexico
Albuquerque, New Mexico, 87109, United States
Retina Vitreous Surgeons of Central NY, PC
Liverpool, New York, 13088, United States
Ophthalmic Consultants of Long Island
Oceanside, New York, 11572, United States
Retina Vitreous Center in Edmond Oklahoma
Edmond, Oklahoma, 73013, United States
Eye Health Northwest
Portland, Oregon, 97225, United States
Eye Care Specialists
Kingston, Pennsylvania, 18704, United States
Charleston Neuroscience Institute (RCA Network Site)
Ladson, South Carolina, 29456, United States
Black Hills Regional Eye Institute - Ophthalmology
Rapid City, South Dakota, 57701, United States
Charles Retina Institute
Germantown, Tennessee, 38138, United States
Retina Research Institute of Texas
Abilene, Texas, 79606, United States
Austin Retina Associates - Ophthalmology/Retina (RCA Network site)
Austin, Texas, 78705, United States
Austin Clinical Research, LLC
Austin, Texas, 78750, United States
Retina Consultants of Texas
Bellaire, Texas, 77401, United States
Texas Retina Associates
Fort Worth, Texas, 76104, United States
Retinal Consultants of Texas- San Antonio (RCA Network site)
San Antonio, Texas, 78240, United States
Retina Consultants of Texas (RCA Network Site)
The Woodlands, Texas, 77384, United States
Strategic Clinical Research Group, LLC
Willow Park, Texas, 76087, United States
Retina Group of Washington
Fairfax, Virginia, 22031, United States
Eye Clinic Albury Wodonga
Albury, New South Wales, 2640, Australia
Marsden Eye Specialists
Parramatta, New South Wales, Australia
Strathfield Retina Clinic
Strathfield, New South Wales, Australia
Sydney Eye Hospital
Sydney, New South Wales, Australia
Adelaide Eye and Retina Centre
Adelaide, South Australia, 5000, Australia
Centre for Eye Research Australia
East Melbourne, Victoria, 3002, Australia
Aichi Medical University Hospital - Ophthalmology
Nagakute, Aichi-ken, 480-1195, Japan
MIYAKE Eye Hospital
Nagoya, Aichi-ken, 462-0825, Japan
Toho University Medical Center Sakura Hospital
Sakura, Chiba, 285-8741, Japan
Matsuyama Red Cross Hospital
Matsuyama, Ehime, 790-8524, Japan
Hayashi Eye Hospital - Ophthalmology
Fukuoka, Fukuoka, 812-0011, Japan
Kurume University Hospital
Kurume, Fukuoka, 830-0011, Japan
Minamitohoku Eye Clinic
Kōriyama, Fukushima, 963-8563, Japan
Caress Sapporo Tokeidai Memorial Hospital
Sapporo, Hokkaido, 060-0031, Japan
Kobe University Hospital - Ophthalmology
Kobe, Hyôgo, 650-0017, Japan
Kozawa Eye Hospital and Diabetes Center
Mito, Ibaraki, 310-0845, Japan
Kagawa University Hospital
Kita-gun, Kanagawa, 761-0793, Japan
Shinshu University Hospital - Ophthalmology
Matsumoto, Nagano, 390-8621, Japan
Nara Medical University Hospital - Ophthalmology
Kashihara, Nara, 634-8522, Japan
University of the Ryukyus Hospital
Nakagami-gun, Okinawa, 903-0215, Japan
Kansai Medical University Medical Center
Hirakata, Osaka, 660-0892, Japan
Kindai University Hospital
Sayama, Osaka, 577-8502, Japan
Jichi Medical University Hospital
Shimotsuke, Tochigi, 329-0498, Japan
The University of Tokyo Hospital
Bunkyō, Tokyo, 113-8655, Japan
Nihon University Hospital
Chiyoda City, Tokyo, 101-8309, Japan
Tokyo Medical University Hachioji Medical Center
Hachiōji, Tokyo, 193-0998, Japan
Tokyo Medical Center
Meguro City, Tokyo, 152-8902, Japan
Keio University Hospital - Ophthalmology
Shinjuku, Tôkyô, 160-8582, Japan
Fukushima Medical University Hospital - Ophthalmology
Fukushima, 960-1295, Japan
Rakuwakai Otowa Hospital
Kyoto, 607-8062, Japan
Okayama University Hospital - Ophthalmology
Okayama, 700-8558, Japan
Saitama Red Cross Hospital
Saitama, 330-8553, Japan
Osaka Metropolitan University Hospital
Osaka, Ôsaka, 545-0051, Japan
Keimyung University Dongsan Hospital
Daegu, Dalseo-gu, 42601, South Korea
Seoul National University Bundang Hospital
Seongnam, Gyeonggido, South Korea
CHA Bundang Medical Center, CHA University
Seongnam-si, Gyeonggido, 13496, South Korea
Yeungnam University Hospital
Daegu, Nam-gu, 42415, South Korea
Gachon University Gil Medical Center
Incheon, Namdong-gu, 21565, South Korea
Kyung Hee University Hospital
Seoul, Seoul Teugbyeolsi, 02447, South Korea
Korea University Anam Hospital
Seoul, Seoul Teugbyeolsi, 02841, South Korea
Seoul National University Hospital
Seoul, Seoul Teugbyeolsi, 03080, South Korea
Severance Hospital, Yonsei University Health System
Seoul, Seoul Teugbyeolsi, 03722, South Korea
Asan Medical Center
Seoul, Seoul Teugbyeolsi, 05505, South Korea
Samsung Medical Center
Seoul, Seoul Teugbyeolsi, 06351, South Korea
The Catholic University of Korea, Seoul St. Mary's Hospital
Seoul, Seoul Teugbyeolsi, 06591, South Korea
Kim Eye Hospital
Seoul, Seoul Teugbyeolsi, 07301, South Korea
MeSH Terms
Interventions
Study Officials
- STUDY DIRECTOR
Sotaro Takigawa
Kyowa Kirin Co., Ltd.
Study Design
- Study Type
- interventional
- Phase
- phase 2
- Allocation
- RANDOMIZED
- Masking
- QUADRUPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
October 31, 2023
First Posted
November 3, 2023
Study Start
January 31, 2024
Primary Completion (Estimated)
August 31, 2026
Study Completion (Estimated)
September 30, 2026
Last Updated
October 30, 2025
Record last verified: 2025-10
Data Sharing
- IPD Sharing
- Will share
The datasets generated and/or analyzed during the study sponsored by Kyowa Kirin will be available in the Vivli repository, https://vivli.org/ourmember/kyowakirin/ as long as conditions of data disclosure specified in the policy section of the Vivli website are satisfied.