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Terminated Phase 3 Interventional Results available

Study of Safety and Efficacy of Brolucizumab 6 mg Dosed Every 4 Weeks Compared to Aflibercept 2 mg Dosed Every 4 Weeks in Patients With Retinal Fluid Despite Frequent Anti-VEGF Injections

ClinicalTrials.gov ID: NCT03710564

Public ClinicalTrials.gov record NCT03710564. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 4:22 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Randomized, Double-masked Phase 3a Study to Assess Safety and Efficacy of Brolucizumab 6 mg q4 Weeks Compared to Aflibercept 2 mg q4 Weeks in Patients With Neovascular Age-related Macular Degeneration (nAMD) With Persistent Retinal Fluid (MERLIN)

Study identification

NCT ID
NCT03710564
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
535 participants

Conditions and interventions

Interventions

  • Brolucizumab Biological
  • Aflibercept Biological

Biological

Eligibility (public fields only)

Age range
50 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 29, 2018
Primary completion
Dec 20, 2020
Completion
Jun 30, 2021
Last update posted
Jan 29, 2023

2018 – 2021

United States locations

U.S. sites
60
U.S. states
25
U.S. cities
54
Facility City State ZIP Site status
Novartis Investigative Site Phoenix Arizona 85016
Novartis Investigative Site Phoenix Arizona 85020
Novartis Investigative Site Phoenix Arizona 85053
Novartis Investigative Site Beverly Hills California 90211
Novartis Investigative Site Huntington Beach California 92647
Novartis Investigative Site Mountain View California 94040
Novartis Investigative Site Oakland California 94609
Novartis Investigative Site Oxnard California 93036
Novartis Investigative Site Palo Alto California 94303
Novartis Investigative Site Redlands California 92374
Novartis Investigative Site Sacramento California 95841
Novartis Investigative Site San Francisco California 94107
Novartis Investigative Site Santa Barbara California 93103
Novartis Investigative Site Colorado Springs Colorado 80909
Novartis Investigative Site Golden Colorado 80401
Novartis Investigative Site Deerfield Beach Florida 33064
Novartis Investigative Site Fort Lauderdale Florida 33308
Novartis Investigative Site Fort Myers Florida 33912-7125
Novartis Investigative Site Miami Florida 33136
Novartis Investigative Site Mt. Dora Florida 32757
Novartis Investigative Site Pensacola Florida 32503
Novartis Investigative Site St. Petersburg Florida 33711
Novartis Investigative Site Stuart Florida 34994
Novartis Investigative Site Marietta Georgia 30060
Novartis Investigative Site ‘Aiea Hawaii 96701
Novartis Investigative Site Wheaton Illinois 60187
Novartis Investigative Site West Des Moines Iowa 50266
Novartis Investigative Site Lenexa Kansas 66215
Novartis Investigative Site New Orleans Louisiana 70115-8139
Novartis Investigative Site West Monroe Louisiana 71291
Novartis Investigative Site Waldorf Maryland 20602
Novartis Investigative Site Boston Massachusetts 02111
Novartis Investigative Site Boston Massachusetts 02114
Novartis Investigative Site Springfield Massachusetts 01107
Novartis Investigative Site Royal Oak Michigan 48073
Novartis Investigative Site St Louis Missouri 63110
Novartis Investigative Site Las Vegas Nevada 89144
Novartis Investigative Site Reno Nevada 89502
Novartis Investigative Site Bloomfield New Jersey 07003
Novartis Investigative Site Toms River New Jersey 08755
Novartis Investigative Site Syracuse New York 13224
Novartis Investigative Site Charlotte North Carolina 28210
Novartis Investigative Site Cleveland Ohio 44122
Novartis Investigative Site Fairfield Ohio 45014
Novartis Investigative Site Eugene Oregon 97401
Novartis Investigative Site Kingston Pennsylvania 95403
Novartis Investigative Site Philadelphia Pennsylvania 19107
Novartis Investigative Site Germantown Tennessee 38138
Novartis Investigative Site Abilene Texas 79606
Novartis Investigative Site Austin Texas 78705
Novartis Investigative Site Austin Texas 78731
Novartis Investigative Site Austin Texas 78793
Novartis Investigative Site Fort Worth Texas 76102
Novartis Investigative Site Fort Worth Texas 76104
Novartis Investigative Site Harlingen Texas 78550
Novartis Investigative Site Houston Texas 77030
Novartis Investigative Site San Antonio Texas 78240
Novartis Investigative Site Tyler Texas 75701
Novartis Investigative Site Fairfax Virginia 22031
Novartis Investigative Site Spokane Washington 99204

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03710564, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 29, 2023 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03710564 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →