Viewing Study NCT00346866


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Study NCT ID: NCT00346866
Status: COMPLETED
Last Update Posted: 2008-08-05
First Post: 2006-06-28
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Anecortave Acetate Versus Placebo in AMD Patients Following PDT
Sponsor: Alcon Research
Organization:

Study Overview

Official Title: Anecortave Acetate Versus Placebo in AMD Patients Following PDT
Status: COMPLETED
Status Verified Date: 2008-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study was to evaluate the efficacy of anecortave acetate for depot suspension (30 mg and 15 mg) plus PDT versus PDT alone with respect to maintenance of visual acuity in patients with wet AMD.
Detailed Description: None

Study Oversight

Has Oversight DMC:
Is a FDA Regulated Drug?:
Is a FDA Regulated Device?:
Is an Unapproved Device?:
Is a PPSD?:
Is a US Export?:
Is an FDA AA801 Violation?: