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Completed Phase 3 Interventional Results available

Efficacy/Safety of Verteporfin Photodynamic Therapy and Ranibizumab Compared With Ranibizumab in Patients With Subfoveal Choroidal Neovascularization

ClinicalTrials.gov ID: NCT00436553

Public ClinicalTrials.gov record NCT00436553. 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, 11:02 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 24-month Randomized, Double-masked, Controlled, Multicenter, Phase IIIB Study Assessing Safety and Efficacy of Verteporfin Photodynamic Therapy Administered in Conjunction With Ranibizumab Versus Ranibizumab Monotherapy in Patients With Subfoveal Choroidal Neovascularization Secondary to Age-related Macular Degeneration

Study identification

NCT ID
NCT00436553
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis
Industry
Enrollment
321 participants

Conditions and interventions

Interventions

  • Verteporfin Photodynamic Therapy Drug
  • Ranibizumab Drug
  • Verteporfin Placebo Drug
  • Ranibizumab Placebo 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
Jan 31, 2007
Primary completion
Sep 30, 2009
Completion
Sep 30, 2009
Last update posted
Apr 18, 2011

2007 – 2009

United States locations

U.S. sites
36
U.S. states
20
U.S. cities
36
Facility City State ZIP Site status
Novartis Investigative Site Tucson Arizona 85704
Novartis Investigative Site Beverly Hills California 90211
Novartis Investigative Site Oakland California 94609
Novartis Investigative Site Pasadena California 91105-3153
Novartis Investigative Site Sacramento California 95819
West Coast Retina Medical Group Inc. - 185 Berry St. Suite 130 San Francisco California 94107
Novartis Investigative Site Santa Ana California 92705
Novartis Investigative Site Denver Colorado 80210
Novartis Investigative Site ‘Aiea Hawaii 96701
Novartis Investigative Site Iowa City Iowa 52242
Novartis Investigative Site Wichita Kansas 67214
Novartis Investigative Site Lexington Kentucky 40509
Novartis Investigative Site Paducah Kentucky 42001
Novartis Investigative Site Baltimore Maryland 21205
Novartis Investigative Site Grand Rapids Michigan 49252
Novartis Investigative SIte Royal Oak Michigan 48073
Novartis Investigative Site Williamsburg Michigan 49690
Novartis Investigative Site Independence Missouri 64055
Novartis Investigative Site St Louis Missouri 63110
Novartis Investigative Site Toms River New Jersey 08755
Novartis Investigative Site Lynbrook New York 11563
Novartis Investigative Site Rochester New York 14620
Novartis Investigative Site Beachwood Ohio 44122
Novartis Investigative Site Cincinnati Ohio 45242
Novartis Investigative Site Cleveland Ohio 44195
Novartis Investigative Site Pittsburgh Pennsylvania 15213
Novartis Investigative Site West Mifflin Pennsylvania 15122
Novartis Investigative Site West Columbia South Carolina 29169
Novartis Investigative Site Rapid City South Dakota 57701
Novartis Investigative Site Kingsport Tennessee 37660
Novartis Investigative Site Knoxville Tennessee 37909
Novartis Investigative Site Austin Texas 78705
Novartis Investigative Site Houston Texas 77030
Novartis Investigative Site Fairfax Virginia 22031
Novartis Investigative Site Richmond Virginia 23226
Novartis Investigative Site Milwaukee Wisconsin 53226

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 7 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00436553, 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 Apr 18, 2011 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00436553 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →