Treatment With Intravitreal Aflibercept Injection For Proliferative Diabetic Retinopathy, The A.C.T Study
Treatment With Intravitreal Aflibercept Injection For Proliferative Diabetic Retinopathy, The A.C.T Study
To assess the safety of intravitreal aflibercept injection in the treatment of proliferative diabetic retinopathy (PDR) by evaluating the incidence and severity of adverse events.
Inclusion Criteria:
Subjects will be enrolled if the following criteria are met:
Exclusion Criteria:
Pregnant or breast-feeding women Sexually active men* or women of childbearing potential** who are unwilling to practice adequate contraception during the study and for at least 30 days after the last administration of study drug for women and at least 90 days after the last administration for men (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];; vasectomy; condom plus contraceptive sponge, foam, or jelly, or diaphragm plus contraceptive sponge, foam, or jelly)
*Contraception is not required for men with documented vasectomy.
** Pregnancy testing and contraception are not required for women with documented hysterectomy.
HbA1C >10 within approximately 90 days of Screening visit
Participation in a study of an investigational drug or device within 30 days prior to potential enrollment into the study
Prior treatment with systemic anti-VEGF agents
Presence of any substantial ocular disease (other than diabetic retinopathy) that may compromise vision in the study eye and /or confound interpretation of the data; e.g. substantial cataracts, advanced glaucoma, optic neuritis, optic neuropathy or atrophy, marked macular atrophy, ocular vascular occlusion, history of retinal detachment, uveitis, viral or other forms of chorioretinitis, etc.
Prior treatment with anti-VEGF therapy in the study eye within 90 days of baseline
Prior treatment with PRP within 60 days
Prior treatment with IAI.
Prior treatment with triamcinolone in the study eye within 180 days of baseline.
Prior treatment with dexamethasone in the study eye within 30 days prior to baseline.
Intraocular surgery (including cataract surgery) in the study eye within 60 days preceding baseline
History of vitrectomy surgery in the study eye.
Active intraocular inflammation (grade trace or above) 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
Uncontrolled glaucoma in the study eye (defined as IOP ≥ 25 mmHg despite treatment with anti-glaucoma medication)
History of cerebral vascular accident, myocardial infarction, transient ischemic attacks within 180 days of study enrollment.
History of allergy to fluorescein, topical antibiotic, povidone iodine (Betadine) or aflibercept.
Presence of vitreous hemorrhage that completely obstructs the view of the optic nerve (amount of vitreous hemorrhage will also be gated by 20/320 criteria)
Presence of TRD in the study eye.
Presence of pre-retinal fibrosis (not including epiretinal membrane)
Unwilling to discontinue sperm bank donation for any period of time after IAI treatment