A Clinical Trial of EYE201/MK-8748 in People With Macular Degeneration (MK-8748-002)
MALBEC
A Randomized Double-masked, Multicenter, 3-arm, Pivotal Phase 2/3 Study to Evaluate the Efficacy and Safety of Intravitreal (IVT) EYE201/MK-8748 Compared to Aflibercept (2 mg) in Participants With Neovascular Age-related Macular Degeneration (NVAMD)
1 other identifier
interventional
960
8 countries
91
Brief Summary
Researchers are looking for new ways to treat neovascular age-related macular degeneration (NVAMD). Available standard (usual) treatments for NVAMD, such as aflibercept, may not work for every person. Researchers want to learn if a trial medicine called tiespectus (also called MK-8748 or EYE201) can treat NVAMD. The goal of this trial is to learn if tiespectus works as well as aflibercept to treat NVAMD.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for phase_2
Started Mar 2026
91 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 23, 2026
CompletedFirst Posted
Study publicly available on registry
February 27, 2026
CompletedStudy Start
First participant enrolled
March 27, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2028
ExpectedStudy Completion
Last participant's last visit for all outcomes
June 30, 2028
July 24, 2026
July 1, 2026
2.3 years
February 23, 2026
July 22, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Mean Change in Best-Corrected Visual Acuity (BCVA) [Early Treatment of Diabetic Retinopathy Study (ETDRS Letters)] From Baseline to Year 1
Participants' BCVA in the study eye will be measured using the Early Treatment of Diabetic Retinopathy (ETDRS) methodology. The ETDRS letter score ranges from 0 to 100, with a higher score indicating better visual acuity. Mean change in ETDRS letters from baseline to Year 1 will be assessed.
Baseline and Year 1
Secondary Outcomes (10)
Mean Change in BCVA (ETDRS Letters) From Baseline (Day 1) Over Time to Year 1
Up to Year 1
Proportion of Participants Who Gain ≥5 ETDRS Letters at Year 1
Year 1
Proportion of Participants Who Gain ≥10 ETDRS Letters at Year 1
Year 1
Proportion of Participants Who Gain ≥15 ETDRS Letters at Year 1
Year 1
Proportion of Participants Who Lose ≥5 ETDRS Letters at Year 1
Year 1
- +5 more secondary outcomes
Study Arms (3)
Tiespectus Low Dose
EXPERIMENTALParticipants receive 3 initial administrations of tiespectus low dose every 4 weeks (Q4W), then continue to receive tiespectus low dose every 8 weeks (Q8W) until week 48. After week 48, participants will be treated at intervals determined based on individualized response to treatment, up to week 92.
Tiespectus High Dose
EXPERIMENTALParticipants receive 3 initial administrations of tiespectus high dose Q4W, then continue to receive tiespectus high dose Q8W until week 48. After week 48, participants will be treated at intervals determined based on individualized response to treatment, up to week 92
Aflibercept 2 mg
ACTIVE COMPARATORParticipants receive 3 initial administrations of aflibercept, then continue to receive aflibercept Q8W until week 92
Interventions
Administered by intravitreal (IVT) injection
Eligibility Criteria
You may qualify if:
- Has treatment naive choroidal neovascularization (CNV) secondary to age-related macular degeneration (AMD) including subfoveal, juxtafoveal and extrafoveal lesions or retinal angiomatous proliferations (RAP) and polypoidal choroidal vascularization (PCV) lesions in at least one eye (study eye)
- The diagnosis of neovascular age-related macular degeneration (NVAMD) must have been made within 21 days prior to starting study treatment
You may not qualify if:
- Has uncontrolled blood pressure at screening
- History of any prior macular laser photocoagulation in the study eye
- History of uveitis in either eye
- History of cataract surgery, minimally invasive glaucoma surgery, or Yttrium-Aluminium Garnet (Yag) laser capsulotomy in the study eye within 90 days before entering the study
- Has uncontrolled glaucoma in the study eye
- Active retinal disease other than the condition under investigation in the study eye
- Has previously received anti- vascular endothelial growth factor (VEGF) therapy or other intravitreal (IVT) therapy in the study eye
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- EyeBiotech Ltd.lead
Study Sites (91)
Research Network Arizona / Retina Macula Institute of Arizona
Scottsdale, Arizona, 85255, United States
Retina Center of Arkansas
Fayetteville, Arkansas, 72703, United States
Retina Partners of Northwest Arkansas, PLLC
Springdale, Arkansas, 72764, United States
Global Research Management, Inc.
Glendale, California, 91204, United States
Retinal Consultants Medical Group (Site 024)
Modesto, California, 95356, United States
Retina Consultants of Southern California (Site 043)
Redlands, California, 92374, United States
Retinal Consultants Medical Group (Site 020)
Sacramento, California, 95825, United States
Retinal Consultants Medical Group (Site 022)
Sacramento, California, 95841, United States
Florida Eye Clinic (Site 130)
Altamonte Springs, Florida, 32701, United States
Retina Group of Florida (Site 070)
Fort Lauderdale, Florida, 33308, United States
Vitreo Retinal Associates
Gainesville, Florida, 32607, United States
Fort Lauderdale Eye Institute (Site 042)
Plantation, Florida, 33324, United States
Retina Vitreous Associates of Florida (Site 049)
St. Petersburg, Florida, 33711, United States
Southern Vitreoretinal Associates
Tallahassee, Florida, 32308, United States
Retina Associates of Florida, LLC
Tampa, Florida, 33609, United States
Retina Vitreous Associates of Florida
Tampa, Florida, 33617, United States
Wildwood Clinical Research / Florida Retina Institute
Wildwood, Florida, 34785, United States
Illinois Retina Associates
Oak Park, Illinois, 60304, United States
Springfield Clinic
Springfield, Illinois, 62703, United States
Associated Vitreoretinal and Uveitis Consultants
Carmel, Indiana, 46032, United States
Cumberland Valley Retina Consultants (Site 007)
Hagerstown, Maryland, 21740, United States
Foundation for Vision Research (Site 073)
Grand Rapids, Michigan, 49546, United States
Mississippi Retina Associates (Site 084)
Madison, Mississippi, 39110, United States
Mid Atlantic Retina
Cherry Hill, New Jersey, 08034, United States
ong Island Vitreoretinal Consultants / Vitreoretinal Consultants of NY (Site 105)
Hauppauge, New York, 11788, United States
Retina Vitreous Surgeons of CNY, PC (Site 033)
Liverpool, New York, 13088, United States
Piedmont Retina Specialists - Winston-Salem
Winston-Salem, North Carolina, 27103, United States
Cincinnati Eye Institute (Site 133)
Cincinnati, Ohio, 45242, United States
Tulsa Retina Consultants
Tulsa, Oklahoma, 74114, United States
Retina Northwest, PC
Portland, Oregon, 97221, United States
EyeHealth Northwest
Portland, Oregon, 97225, United States
Mid Atlantic Retina (Site 050)
Bethlehem, Pennsylvania, 18017, United States
Palmetto Retina Center
Aiken, South Carolina, 29803, United States
Charleston Neuroscience Institute - Bluffton (Site 124)
Bluffton, South Carolina, 29910, United States
Charleston Neuroscience Institute (Site 104)
Charleston, South Carolina, 29414, United States
Charleston Neuroscience Institute (CNI) d/b/a Retina Consultants of South Carolina
Mt. Pleasant, South Carolina, 29464, United States
Charles Retina Institute
Germantown, Tennessee, 38138, United States
Retina Research Institute of Texas (Site 010)
Abilene, Texas, 79606, United States
Southwest Retina Specialists
Amarillo, Texas, 79106, United States
Texas Retina Associates
Arlington, Texas, 76012, United States
Austin Research Center for Retina
Austin, Texas, 78705, United States
Austin Retina Associates (Site 012)
Austin, Texas, 78705, United States
Retina & Vitreous of Texas
Bellaire, Texas, 77401, United States
Texas Retina Associates
Dallas, Texas, 75231, United States
Texas Retina (Site 037)
Plano, Texas, 75075, United States
Retina Center of Texas
Southlake, Texas, 76092, United States
Retina Consultants of Texas (Site 014)
The Woodlands, Texas, 77384, United States
Strategic Clinical Research Group
Weatherford, Texas, 76087, United States
Retina Associates of Utah
Salt Lake City, Utah, 84107, United States
Piedmont Eye Center (Site 054)
Lynchburg, Virginia, 24502, United States
Pacific Northwest Retina (Site 112)
Burlington, Washington, 98233, United States
Spokane Eye Clinical Research (Site 075)
Spokane, Washington, 99204, United States
Retina Consultants, PLLC
Charleston, West Virginia, 25301, United States
Grupo Laser Vision (Rosario Eximer Laser Vision SA)
Rosario, Santa Fe Province, S2000DLA, Argentina
Oftalmología Global (Centro Médico Oftalmología Global) (Site 304)
Rosario, Santa Fe Province, S2000DSK, Argentina
Microcirugia Ocular Rosario (Site 310)
Rosario, Santa Fe Province, S2000TC, Argentina
Centro de Ojos Quilmes
Buenos Aires, B1878KDF, Argentina
Fundacion Jorge Zambrano para la investigación, diagnostivo y tratamiento de enfermedades oculares (Site 302)
Buenos Aires, C1023AAQ, Argentina
RSresearch (Site 308)
Buenos Aires, C1033AAW, Argentina
Instituto Oftalmologico de Buenos Aires SA (Site 306)
Buenos Aires, C1120AAN, Argentina
Centro Oftalmologico Dr Charles y Asociados (Site 300)
Buenos Aires, C1121ABB, Argentina
Centro de Ojos Loria SRL (Site 312)
Buenos Aires, CP1832, Argentina
Centro Oftalmológico Dr. Zas
Buenos Aires, PC1023, Argentina
Instituto Donato
Cdad. Autónoma de Buenos Aires, C1428, Argentina
Instituto de Microcirugía Ocular Córdoba (IMOC S.R.L) (Site 305)
Córdoba, 5000, Argentina
Centro Privado de Ojos Romagosa SA (Site 307)
Córdoba, X5000AAI, Argentina
Centrovision Clinica Oftalmologica
Mendoza, 5500, Argentina
Oftar Centro De Oftalmología en Mendoza
Mendoza, 5500, Argentina
Centro de la Visión (Site 309)
Salta, A4400, Argentina
Instituto Zeman Bardeci (Site 311)
Salta, A4400, Argentina
Eye Clinic Albury Wodonga (Site 425)
Albury, 2640 NSW, Australia
Marsden Eye Specialists (Site 420)
Parramatta, 2150, NSW, Australia
Marsden Eye Specialists (Site 423)
Strathfield, 2135 NSW, Australia
Sydney Eye Hospital (Site 426)
Sydney, 2000 NSW, Australia
Sydney Retina Clinic and Day Surgery (Site 424)
Sydney, 2000, NSW, Australia
Barzilai Medical Center
Ashkelon, 7830604, Israel
Rambam Health Corporation (Site 706)
Haifa, 3109601, Israel
Carmel Medical Center (Site 704)
Haifa, 3436212, Israel
Hadassah Medical Center Opthalmology Department (Site 701)
Jerusalem, 9112001, Israel
Rabin Medical Center (Site 700)
Petah Tikva, 49100, Israel
Sheba Medical Center (Site 707)
Ramat Gan, 6265601, Israel
Kaplan Medical Center Ophthalmology Department (Site 705)
Rehovot, 7661005, Israel
Shamir Medical Center (Site 703)
Ẕerifin, 7033001, Israel
P.Stradins clinical university hospital
Riga, LV1002, Latvia
Clinica de Oftalmologia Barraquer
Barcelona, 08021, Spain
University Hospital Basel, Eye Clinic
Basel, CH-4031, Switzerland
Swiss Eye Institute and Berner Augenklinik
Bern, CH-3007, Switzerland
Vista Augenklinik Binningen
Binnigen, CH-4102, Switzerland
Stadtspital Zurich Triemli Forschungszentrum Augenklinik
Zurich, CH-8063, Switzerland
University Hospitals of Leicester NHS Trust (Site 209)
Leicester, LE1 5WW, United Kingdom
London North West University Healthcare NHS Trust (LNWH) (Site 201)
London, NW10 7NS, United Kingdom
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Medical Director
Merck Sharp & Dohme LLC
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- phase 2
- Allocation
- RANDOMIZED
- Masking
- TRIPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, INVESTIGATOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 23, 2026
First Posted
February 27, 2026
Study Start
March 27, 2026
Primary Completion (Estimated)
June 30, 2028
Study Completion (Estimated)
June 30, 2028
Last Updated
July 24, 2026
Record last verified: 2026-07