Safety and Efficacy Study of rAAV.sFlt-1 in Patients With Exudative Age-Related Macular Degeneration (AMD)

Lions Eye Institute, Perth, Western Australia

Status and phase

Completed

Phase 2

Phase 1

Conditions

Retinal Neovascularization

Age-related Maculopathy

Macular Degeneration

Age-related Maculopathies

Retinal Degeneration

Maculopathies,Age-related

Maculopathy,Age-related

Eye Diseases

Treatments

Biological: rAAV.sFlt-1

Other: Control (ranibizumab alone)

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT01494805

2008-135

Details and patient eligibility

About

The study will involve approximately 40 subjects aged 55 or above who have exudative age-related macular degeneration (wet AMD). Patients will be randomized to receive one of two doses of rAAV.sFlt-1 or assigned to the control group.

Full description

A new treatment for exudative age-related macular degeneration (wet AMD) is being investigated. The purpose of this Phase I/II clinical research study is to examine the baseline safety and efficacy of an experimental study drug to treat a complication of the disease which leads to vision loss. The name of the study drug is rAAV.sFlt-1.

This experimental study uses a non-pathogenic virus to express a therapeutic protein within the eye. The therapeutic diminishes the growth of abnormal blood vessels under the retina. The duration of effect is thought to be long-term (years) following a single administration.

The clinical research study will look at the baseline safety and efficacy of a single injection of rAAV.sFlt-1 injected directly into the eye.

Approximately forty (40) subjects will participate in Australia. The primary endpoint of the study is at one month, with extended follow up for 3 years.

Enrollment

40 patients

Sex

All

Ages

55+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Age greater than or equal to 55 years;
Subfoveal CNV secondary to AMD and with best corrected visual acuity of 3/60 - 6/9 with 6/60 or better in the other eye;
Fluorescein angiogram of the study eye must show evidence of a leaking subfoveal choroidal neovascular lesion, or CNV currently under active management with anti-VEGF therapy;
Must be a candidate for anti-VEGF intravitreal injections;
No previous retinal treatment of photodynamic therapy or laser;
Able to provide informed consent;
Able to comply with protocol requirements, including follow-up visits.

Exclusion criteria

Liver enzymes > 2 X upper limit of normal;
Any prior treatment for AMD in the study / control eye, excluding anti-VEGF injections;
Extensive sub-foveal scarring, extensive geographic atrophy, or thick subretinal blood in the study eye as determined by the investigator;
Significant retinal disease other than sub-foveal CNV AMD;