Clinical Trials Directory

Trials / No Longer Available

No Longer AvailableNCT01714115

Use of Eylea for the Treatment of an Optic Nerve Hemangioma

Status
No Longer Available
Phase
Study type
Expanded Access
Enrollment
Sponsor
Vitreous -Retina- Macula Consultants of New York · Academic / Other
Sex
Male
Age
18 Years
Healthy volunteers

Summary

This is a single patient investigative treatment study. The patient was diagnosed with a retinal tumor in one eye. In the last 2 years, the patient has been treated with all available and conventional therapies, including intraocular injections of Avastin and Lucentis, steroids, and photodynamic therapy. Any positive results were short-term, and caused an eventual decline in central vision. Aflibercept has been shown to be effective against the growth of new vessels, secondary to macular degeneration. This study proposes that it may also be more effective in treating this particular patient and case. The study treatment plan is for 6 months initially, with the intention to continue treatment.

Detailed description

The treatment plan will be to administer aflibercept 2.0 mg intravitreally every two to four weeks for at least six consecutive injections. Prior to initiation of therapy and at each study visit, a full ophthalmic examination, best-corrected visual acuity, and a complete review of systems to monitor for any toxicity will be performed. In addition, the investigators will perform fluorescein and indocyanine green angiography at baseline and obtain color fundus photographs as well as spectral domain OCT images to properly document the extent and degree of activity of the vascular tumor at baseline and at all study visits.

Conditions

Interventions

TypeNameDescription
DRUGAflibercept2.0 mg Intravitreal Injection, every 2 to 4 weeks

Timeline

First posted
2012-10-25
Last updated
2017-08-08

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01714115. Inclusion in this directory is not an endorsement.