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Completed Phase 3 Interventional Results available

Study of Efficacy and Safety of Brolucizumab vs. Aflibercept in Patients With Visual Impairment Due to Diabetic Macular Edema

ClinicalTrials.gov ID: NCT03481634

Public ClinicalTrials.gov record NCT03481634. 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 May 11, 2026, 3:07 AM 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 Two-year, Three-arm, Randomized, Double-masked, Multicenter, Phase III Study Assessing the Efficacy and Safety of Brolucizumab Versus Aflibercept in Adult Patients With Visual Impairment Due to Diabetic Macular Edema

Study identification

NCT ID
NCT03481634
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
566 participants

Conditions and interventions

Interventions

  • Aflibercept Drug
  • Brolucizumab Drug

Drug

Eligibility (public fields only)

Age range
18 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
Jul 22, 2018
Primary completion
Nov 10, 2020
Completion
Oct 17, 2021
Last update posted
Jan 29, 2023

2018 – 2021

United States locations

U.S. sites
39
U.S. states
18
U.S. cities
36
Facility City State ZIP Site status
Novartis Investigative Site Phoenix Arizona 85053
Novartis Investigative Site Beverly Hills California 90211
Novartis Investigative Site La Jolla California 92093
Novartis Investigative Site Mountain View California 94040
Novartis Investigative Site Santa Barbara California 93103
Novartis Investigative Site Colorado Springs Colorado 80909
Novartis Investigative Site Danbury Connecticut 06810
Novartis Investigative Site Miami Florida 33136
Novartis Investigative Site Pensacola Florida 32503
Novartis Investigative Site Stuart Florida 34994
Novartis Investigative Site ‘Aiea Hawaii 96701
Novartis Investigative Site Urbana Illinois 61801
Novartis Investigative Site Wheaton Illinois 60187
Novartis Investigative Site Indianapolis Indiana 46280
Novartis Investigative Site New Albany Indiana 47150
Novartis Investigative Site Leawood Kansas 66211
Novartis Investigative Site Lenexa Kansas 66215
Novartis Investigative Site Paducah Kentucky 42001
Novartis Investigative Site Springfield Massachusetts 01107
Novartis Investigative Site Stoneham Massachusetts 02180
Novartis Investigative Site Reno Nevada 89502
Novartis Investigative Site Cincinnati Ohio 45242
Novartis Investigative Site Cleveland Ohio 44122
Novartis Investigative Site Cleveland Ohio 44195
Novartis Investigative Site Kingston Pennsylvania 95403
Novartis Investigative Site Philadelphia Pennsylvania 19107
Novartis Investigative Site Memphis Tennessee 38119
Novartis Investigative Site Nashville Tennessee 37232
Novartis Investigative Site Austin Texas 78705
Novartis Investigative Site Austin Texas 78731
Novartis Investigative Site Austin Texas 78750
Novartis Investigative Site Bellaire Texas 77401
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 Silverdale Washington 98383
Novartis Investigative Site Spokane Washington 99204
Novartis Investigative Site Madison Wisconsin 53705-3611

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 77 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03481634, 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 May 11, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03481634 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →