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Terminated Phase 3 Interventional Results available

A Phase 3 Safety and Efficacy Study of Fovista® (E10030) Intravitreous Administration in Combination With Lucentis® Compared to Lucentis® Monotherapy

ClinicalTrials.gov ID: NCT01944839

Public ClinicalTrials.gov record NCT01944839. 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, 9:38 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 Phase 3 Randomized, Double-masked, Controlled Trial to Establish the Safety and Efficacy of Intravitreous Administration of Fovista® (Anti PDGF-B Pegylated Aptamer) Administered in Combination With Lucentis® Compared to Lucentis® Monotherapy in Subjects With Subfoveal Neovascular Age-related Macular Degeneration.

Study identification

NCT ID
NCT01944839
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Ophthotech Corporation
Industry
Enrollment
619 participants

Conditions and interventions

Interventions

  • E10030 Drug
  • ranibizumab Drug
  • E10030 sham intravitreal injection Drug

Drug

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
Jul 31, 2013
Primary completion
Nov 30, 2016
Completion
Nov 30, 2016
Last update posted
Oct 29, 2024

2013 – 2016

United States locations

U.S. sites
50
U.S. states
30
U.S. cities
47
Facility City State ZIP Site status
Not listed Phoenix Arizona 85014
Not listed Bakersfield California 93309
Not listed Beverly Hills California 90211
Not listed Los Angeles California 90095
Not listed San Francisco California 94107
Not listed Santa Barbara California 93103
Not listed Colorado Springs Colorado 80909
Not listed Bridgeport Connecticut 06606
Not listed New London Connecticut 06320
Not listed Altamonte Springs Florida 32701
Not listed Fort Myers Florida 33907
Not listed Sarasota Florida 34233
Not listed Tampa Florida 33609
Not listed Tampa Florida 33612
Not listed Winter Haven Florida 33880
Not listed Marietta Georgia 30060
Not listed Springfield Illinois 62704-2173
Not listed Indianapolis Indiana 46290
Not listed Leawood Kansas 66211
Not listed Lexington Kentucky 40509
Not listed Lexington Kentucky 40536
Not listed Louisville Kentucky 40202
Not listed New Orleans Louisiana 70121
Not listed Chevy Chase Maryland 20815
Not listed Boston Massachusetts 02111
Not listed Boston Massachusetts 02114
Not listed Jackson Michigan 49202
Not listed Southfield Michigan 48034
Not listed Rochester Minnesota 55905
Not listed St Louis Missouri 63110
Not listed Las Vegas Nevada 89135
Not listed Portsmouth New Hampshire 03801
Not listed Northfield New Jersey 08225
Not listed Albuquerque New Mexico 87109
Not listed Great Neck New York 11021
Not listed Shirley New York 11967
Not listed Cincinnati Ohio 45242
Not listed Cleveland Ohio 44195
Not listed Ashland Oregon 97520
Not listed Camp Hill Pennsylvania 17011
Not listed Philadelphia Pennsylvania 19107
Not listed Pittsburgh Pennsylvania 15212
Not listed Ladson South Carolina 29456
Not listed Nashville Tennessee 37232
Not listed Abilene Texas 79606
Not listed Austin Texas 78705
Not listed Tyler Texas 75701
Not listed Salt Lake City Utah 84132
Not listed Fairfax Virginia 22031
Not listed Madison Wisconsin 53705

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 65 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01944839, 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 29, 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 NCT01944839 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →