Repeated Eye Injections of Aflibercept for Treatment of Wet Age Related Macular Degeneration

Completed · Not applicable

Conditions studied: Age-Related Macular Degeneration, Macular Degeneration

In brief

To evaluate the visual outcome and number of injections required during an optical coherence tomography (OCT)-guided treat and extend regimen with intravitreal aflibercept for treatment of subfoveal neovascular age-related macular degeneration (NVAMD).

Key facts

Study ID

NCT01773954

Run by

MidAtlantic Retina

People needed

40

Starts

2013-02-01

Expected to finish

2016-03-01

Last updated by the study team

2018-05-02

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients older than 55 years with treatment naïve, active subfoveal NVAMD demonstrating macular fluid on optical coherence tomography (OCT) and leakage on fluorescein angiography (FA).
• Only one eye for each patient demonstrating a pre-treatment acuity of 20/25 - 20/320 is eligible
• Patients cannot have concurrent progressive retinal disease in the study eye.
• Willing and able to comply with clinic visits and study-related procedures
• Provide signed informed consent

You may not qualify if…

• Prior treatment for NVAMD in the study eye,
• Prior experimental treatment of NVAMD in either eye
• Prior treatment with systemic anti-VEGF (vascular endothelial growth factor) agents
• Prior treatment with verteporfin, plaque brachytherapy, or external-beam radiation therapy, or transpupillary thermotherapy in the study eye
• Previous subfoveal focal laser photocoagulation involving the foveal center in the study eye
• History of vitreo surgical intervention in the study eye. Cataract surgery is permitted.
• Concurrent eye disease in the study eye that could compromise visual acuity (e.g. diabetic retinopathy, advanced glaucoma)
• Any concurrent intraocular condition in the study eye (e.g. diabetic retinopathy or glaucoma) that, in the opinion of the investigator, could either
• require medical or surgical intervention during the 52 weeks study period to prevent or treat visual loss that might result from that condition, or
• allowed to progress untreated, could likely contribute to loss of at least 2 Snellen equivalent lines of best corrected visual acuity over the 52 weeks study period
• Active intraocular inflammation (grade trace or above) in the study eye, or history of idiopathic or autoimmune-associated uveitis in either eye
• Current vitreous hemorrhage in the study eye
• History of rhegmatogenous retinal detachment or macular hole (Stage 3 or 4) in the study eye
• Active infectious conjunctivitis, keratitis, scleritis, or endophthalmitis in either eye
• Aphakia, Anterior Chamber Intraocular Lens (ACIOL), or unstable Posterior Chamber Intraocular Lens (PCIOL).
• Uncontrolled glaucoma in the study eye (defined as intraocular pressure ≥30 mmHg despite treatment with anti-glaucoma medication)
• Pregnant or breast-feeding women
• Sexually active men* or women of childbearing potential** who are unwilling to practice adequate contraception during the study (adequate contraceptive measures include stable use of oral contraceptives or other prescription pharmaceutical contraceptives for 2 or more menstrual cycles prior to screening; intrauterine device [IUD]; bilateral tubal ligation; vasectomy; condom plus contraceptive sponge, foam, or jelly, or diaphragm plus contraceptive sponge, foam, or jelly)

Where it is running

• Mid Atlantic Retina- Cherry Hill — Cherry Hill, New Jersey, United States
• Mid Atlantic Retina- Huntingdon Valley — Huntingdon Valley, Pennsylvania, United States
• Mid Atlantic Retina- Wills Eye Institute — Philadelphia, Pennsylvania, United States

Full record on ClinicalTrials.gov

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