Clinical Trials Directory

Trials / Completed

CompletedNCT00211484

Treatment of Conditions With Open Label-Anecortave Acetate Sterile Suspension ( 15mg.) Where Lesions do Not Meet Acceptable Criteria for Standard Care.

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
5 (actual)
Sponsor
Manhattan Eye, Ear & Throat Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers

Summary

A compassionate method of treatment is offered to patients where lesions do not meet acceptable criteria for standard therapy. Visudyne (Photodynamic Therapy) and laser photocoagulation treatment (a treatment using heat from a fine point laser beam) have not been found to be effective in treating the lesions these patients have. Anecortave acetate is an experimental drug that is being tested to prevent the growth of blood vessels under the retina in patients with age-related macular degeneration (AMD).

Detailed description

Patients will receive a sub-Tenon injection of 15mg of Anecortave acetate in their study eye with the use of a counter pressure device. Patients will then be followed for up to 24 months. The patients will have the option of extending their participation in the study for an additional 24 months. Statistical analysis will include comparison of patient follow-up visual acuity and angiographic data.

Conditions

Interventions

TypeNameDescription
DRUGAnecortave Acetate

Timeline

Start date
2003-05-01
Completion
2007-03-01
First posted
2005-09-21
Last updated
2007-05-07

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00211484. Inclusion in this directory is not an endorsement.