EAGLE: Evaluating Genotypes Using Intravitreal Aflibercept Injection

Completed · Phase 4

Conditions studied: Macular Degeneration, Wet Macular Degeneration

In brief

Clinical and genetic evaluation of individuals treated with intravitreal aflibercept injection (Eylea) for neovascular age-related macular degeneration (wet AMD)

Key facts

Study ID

NCT02689518

Run by

University of California, San Diego

People needed

50

Starts

2014-04-01

Expected to finish

2019-11-12

Last updated by the study team

2021-03-25

Who can join

Age: 50 and older, up to 90. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Age ≥ 50 years
• Naïve neovascular wet-AMD (has not received treatment before)
• Willing and able to comply with clinic visits and study-related procedures
• Provide signed informed consent

You may not qualify if…

• Previous therapy in study eye for AMD or other retinal disease which may be used in the treatment of AMD
• Previous subfoveal focal laser photocoagulation involving the foveal center in the study eye
• History of vitrectomy, submacular surgery, or other surgical intervention for AMD in the study eye
• Any concurrent intraocular condition in the study eye (e.g. diabetic retinopathy or glaucoma) that, in the opinion of the investigator, could either 4.1 require medical or surgical intervention during the study period to prevent or treat visual loss that might result from that condition, or 4.2 if allowed to progress untreated, could likely contribute to loss of at least 2 Snellen equivalent lines of best corrected visual acuity over the 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, ACIOL, or unstable 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)
• Any other condition that the investigator believes would pose a significant hazard to the patient if the investigational therapy were initiated *Contraception is not required for men with documented vasectomy. **Postmenopausal women must be amenorrheic for at least 12 months in order not to be considered of child bearing potential. Pregnancy testing and contraception are not required for women with documented hysterectomy or tubal ligation.

Where it is running

• Shiley Eye Center — La Jolla, California, United States

Full record on ClinicalTrials.gov

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