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Completed Phase 3 Interventional Results available

Study to Assess the Efficacy and Safety of Brolucizumab 6mg Compared to Aflibercept 2 mg in a Treat-to-control Regimen (TALON)

ClinicalTrials.gov ID: NCT04005352

Public ClinicalTrials.gov record NCT04005352. 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 22, 2026, 9:37 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 64-week, Two-arm, Randomized, Double-masked, Multicenter, Phase IIIb Study Assessing the Efficacy and Safety of Brolucizumab 6 mg Compared to Aflibercept 2 mg in a Treat-to-control Regimen in Patients With Neovascular Agerelated Macular Degeneration (TALON)

Study identification

NCT ID
NCT04005352
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
734 participants

Conditions and interventions

Interventions

  • Brolucizumab 6 mg Biological
  • Aflibercept 2 mg 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
Sep 24, 2019
Primary completion
Sep 8, 2022
Completion
Sep 8, 2022
Last update posted
Oct 8, 2024

2019 – 2022

United States locations

U.S. sites
24
U.S. states
11
U.S. cities
23
Facility City State ZIP Site status
Novartis Investigative Site Phoenix Arizona 85020
Novartis Investigative Site Huntington Beach California 92647
Novartis Investigative Site Loma Linda California 92354
Novartis Investigative Site Riverside California 92505
Novartis Investigative Site Santa Ana California 92705
Novartis Investigative Site Fort Lauderdale Florida 33309
Novartis Investigative Site Fort Myers Florida 33912-7125
Novartis Investigative Site Orlando Florida 32789
Novartis Investigative Site Pinellas Park Florida 33782
Novartis Investigative Site Winter Haven Florida 33880
Novartis Investigative Site Springfield Illinois 62704
Novartis Investigative Site Indianapolis Indiana 46280
Novartis Investigative Site West Des Moines Iowa 50266
Novartis Investigative Site Minneapolis Minnesota 55435
Novartis Investigative Site Hickory North Carolina 28602
Novartis Investigative Site Portland Oregon 97210
Novartis Investigative Site Springfield Oregon 97477
Novartis Investigative Site Germantown Tennessee 38138
Novartis Investigative Site Austin Texas 78705
Novartis Investigative Site Bellaire Texas 77401
Novartis Investigative Site Fort Worth Texas 76104
Novartis Investigative Site Houston Texas 77025
Novartis Investigative Site Houston Texas 77030
Novartis Investigative Site San Antonio Texas 78240

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 94 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04005352, 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 Oct 8, 2024 · Synced Jul 22, 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 NCT04005352 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →