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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00346866
Other study ID # C-00-07
Secondary ID
Status Completed
Phase Phase 2
First received June 28, 2006
Last updated August 4, 2008
Start date May 2000
Est. completion date December 2001

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 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.


Recruitment information / eligibility

Status Completed
Enrollment 136
Est. completion date December 2001
Est. primary completion date December 2001
Accepts healthy volunteers No
Gender Both
Age group 50 Years and older
Eligibility Inclusion Criteria:

- AMD disease

Exclusion Criteria:

- Age

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
anecortave acetate


Locations

Country Name City State
United States Facility Beachwood Ohio

Sponsors (1)

Lead Sponsor Collaborator
Alcon Research

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Mean change from the baseline in logMAR visual acuity score at Month 6
Secondary % patients who maintained vision, number of months of angiographic evidence of needing PDT re-treatment, and mean lesion sizes for the total choroidal neovascularization (CNV) and the classic component to the total CNV.
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