Treatment With Intravitreal Aflibercept Injection For Proliferative Diabetic Retinopathy, The A.C.T Study

- Single center, open label pilot study using 2.0mg intravitreal aflibercept injection.
(IAI)

- 20 subjects with active PDR to be randomized into 2 groups, i.e. groups A and B.

- Subjects in both arms will be followed-up every 4 weeks until week 52.

- The primary endpoint of the study will be at week 52.

Inclusion Criteria:

Subjects will be enrolled if the following criteria are met:

- Ability to provide written informed consent and comply with study assessments for the
full duration of the study

- Age 18 years and older

- Retinal neovascularization secondary to diabetic retinopathy

- Best corrected visual acuity in the study eye better than 20/320 using an ETDRS chart

- In the event that either eye of a potential subject meets enrollment criteria, the
worse sighted eye will be enrolled into the study. Only one eye can be enrolled in
the study.

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