Assessment of Biomarker Profile in Diabetic Macular Edema With Intravitreal Aflibercept Injection



Status:Not yet recruiting
Conditions:Cardiology, Ocular
Therapuetic Areas:Cardiology / Vascular Diseases, Ophthalmology
Healthy:No
Age Range:18 - 89
Updated:10/6/2017
Start Date:December 1, 2017
End Date:March 1, 2020
Contact:Mary M Chatterton, MBA, JD
Email:mmchatterton@gmail.com
Phone:617-834-3660

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Assessment of Biomarker Profile in Diabetic Macular Edema in Response to Treatment With Intravitreal Aflibercept

To assess the biomarker profile in diabetic macular edema patients in response to
intravitreal aflibercept injection. Patients with diabetic macular edema who meet study
requirements will receive monthly intravitreal injections of aflibercept as approved by FDA
for a period of 6 months. A small quantity of fluid will be removed from the vitreous at each
injection for laboratory evaluation of biomarkers present before, during and after treatment
with aflibercept.

Study objective is to better understand the pathophysiology of diabetic macular edema (DME)
by defining the factors that participate in the disease process or may be good biomarkers for
disease progression. Study will investigate the temporal relationship between the course of
treatment with anti-VEGF therapy and levels of candidate biomarkers previously identified to
determine which biomarkers are affected by anti-VEGF therapy with aflibercept. Study will
correlate response to therapy to particular biomarkers and attempt to identify those
associated with resistance to therapy for DME. Biomarker data will be correlated with serial
clinical evaluation of disease progression. 40 subjects with clinically significant DME who
plan to undergo anti-VEGF therapy will be treated with intravitreal aflibercept monthly for 6
months. At each visit aqueous humor will be collected and stored (6 samples per patient). At
termination of study all specimens will be analyzed for biomarkers identified from previous
studies.

Inclusion Criteria:

- Current diagnosis type 1 or type 2 diabetes

- Clinical DME as assessed by OCT

- Well controlled glaucoma on medications but not on prostaglandin analogues

- Mild Age Related Macular Degeneration (AMD)

- Visual acuity between 73 and 5 ETDRS letters (20/40 -20/800 on eye chart)

- Willing and able to participate and to comply with clinic visits and procedures

- Provide signed informed consent

Exclusion Criteria:

- Unwillingness to participate or inability to understand or sign informed consent

- Poor eye fluid that would preclude adequate testing

- Prior intraocular treatment with anti-VEGF or focal laser treatment within 90 days

- Corticosteroid injections within 120 days

- Active proliferative diabetic retinopathy

- Intraocular pressure greater than 25 mm Hg

- Any previous vitrectomy surgery

- Current use of systemic anti-VEGF agents

- Shallow anterior eye chamber in eye with natural lens

- Non-diabetic related macular swelling (retinal vein occlusion)

- History of ocular disease

- Systemic disease other than diabetes mellitus

- Pregnant or breast feeding women

- Sexually active men or women of childbearing potential who are unwilling to practice
adequate birth control during study
We found this trial at
1
site
500 Faunce Corner Road
South Dartmouth, Massachusetts 02747
Phone: 508-717-0270
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mi
from
South Dartmouth, MA
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