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Completed Phase 2 Interventional

Safety and Efficacy Study of Small Interfering Ribonucleic Acid (RNA) Molecule (Cand5) to Treat Wet Age-Related Macular Degeneration

ClinicalTrials.gov ID: NCT00259753

Public ClinicalTrials.gov record NCT00259753. 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, 11:55 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 II, Randomized, Double-Masked, Controlled, Dose Comparison Study of Cand5 for Intravitreal Injection for the Treatment of Subfoveal Choroidal Neovascularization Associated With Wet Age-Related Macular Degeneration

Study identification

NCT ID
NCT00259753
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
OPKO Health, Inc.
Industry
Enrollment
120 participants

Conditions and interventions

Interventions

  • Bevasiranib 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
Jun 30, 2005
Primary completion
Nov 30, 2007
Completion
Nov 30, 2007
Last update posted
Aug 4, 2008

2005 – 2007

United States locations

U.S. sites
23
U.S. states
14
U.S. cities
22
Facility City State ZIP Site status
Acuity Participating Site Phoenix Arizona 85014
Retina Centers PC Tucson Arizona 85704
Sall Research Medical Center Artesia California 90701
Bay Area Retina Associates Walnut Creek California 94598
Florida Eye Microsurgical Institute, Inc. Boynton Beach Florida 33426
Retina Specialist Towson Maryland 21204
Vitreo-Retinal Associates PC Grand Rapids Michigan 49525
Associated Retinal Consultants Grand Rapids Michigan 49546
Associated Retinal Consultants, P.C. Royal Oak Michigan 48073
VitreoRetinal Surgery, P.A. Edina Minnesota 55435
Eye Foundation of Kansas City, UMKC School of Medicine Kansas City Missouri 64108
Retina-Vitreous Center Lakewood New Jersey 08701
Retina-Vitreous Consultants Livingston New Jersey 07039
OCLI Lynbrook New York 11563
LuEsther T. Mertz Retinal Research Center New York New York 10021
Southeast Clinical Research Charlotte North Carolina 28210
Retina Associates of Cleveland Beachwood Ohio 44122
Retina Associates of Cleveland, Inc. Lakewood Ohio 44107
Black Hills Eye Institute Rapid City South Dakota 57701
Retina Reseach Center Austin Texas 78705
Ophthalmology Associates Fort Worth Texas 76102
Vitreoretinal Consultants Houston TX Houston Texas 77030
Medical College of Wisconsin Eye Institute 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.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00259753, 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 Aug 4, 2008 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00259753 live on ClinicalTrials.gov.

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