EAGLE: Evaluating Genotypes Using Intravitreal Aflibercept Injection

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University of California San Diego

Status and phase

Completed
Phase 4

Conditions

Macular Degeneration
Wet Macular Degeneration

Treatments

Drug: Intravitreal aflibercept injection

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT02689518
EAGLE

Details and patient eligibility

About

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

Full description

Clinical and genetic assessment of treatment response in patients with age-related macular degeneration using intravitreal aflibercept injection. This study seeks to determine if different genetic polymorphisms of vascular endothelial growth factor A (VEGF-A) and HtrA serine peptidase 1(HTRA1) and other genes correlate to the response to intravitreal aflibercept injection therapy.

Enrollment

50 patients

Sex

All

Ages

50 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

  1. Previous therapy in study eye for AMD or other retinal disease which may be used in the treatment of AMD
  2. Previous subfoveal focal laser photocoagulation involving the foveal center in the study eye
  3. History of vitrectomy, submacular surgery, or other surgical intervention for AMD in the study eye
  4. 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
  5. Active intraocular inflammation (grade trace or above) in the study eye, or history of idiopathic or autoimmune-associated uveitis in either eye
  6. Current vitreous hemorrhage in the study eye
  7. History of rhegmatogenous retinal detachment or macular hole (Stage 3 or 4) in the study eye
  8. Active infectious conjunctivitis, keratitis, scleritis, or endophthalmitis in either eye
  9. Aphakia, ACIOL, or unstable PCIOL
  10. Uncontrolled glaucoma in the study eye (defined as intraocular pressure ≥30 mmHg despite treatment with anti-glaucoma medication)
  11. Pregnant or breast-feeding women
  12. 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)
  13. 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.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

50 participants in 1 patient group

Treatment - On-Label
Other group
Description:
On-label intravitreal aflibercept (Eylea) injection 2 mg (0.05 mL) administered every 4 weeks for the first 3 months, followed by 2 mg (0.05 mL) intravitreal injection once every 8 weeks (2 months) with the option to treat monthly based on retreatment criteria for a total duration of 12 months
Treatment:
Drug: Intravitreal aflibercept injection

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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