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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00058994
Other study ID # C-02-29
Secondary ID
Status Completed
Phase Phase 3
First received April 15, 2003
Last updated November 28, 2012
Start date March 2003
Est. completion date November 2006

Study information

Verified date August 2008
Source Alcon Research
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

The purpose of this study is to demonstrate that anecortave acetate is superior to placebo in maintenance of visual acuity at the 12- and 24-month visits.


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date November 2006
Est. primary completion date November 2006
Accepts healthy volunteers No
Gender Both
Age group 50 Years and older
Eligibility Patients at least 50 years of age, of any race, and either sex with a clinical diagnosis of exudative AMD and a primary or recurrent subfoveal CNV lesion in the study eye.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Intervention

Drug:
anecortave acetate


Locations

Country Name City State
United States South America Fort Worth Texas

Sponsors (1)

Lead Sponsor Collaborator
Alcon Research

Country where clinical trial is conducted

United States, 

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