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

Diabetic Macular Edema Clinical Trial

Official title:

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

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT03297684
• Other study ID #: AERA101
• Status: Active, not recruiting
• Start date: April 11, 2018
• Est. completion date: December 31, 2022

Study information

• Verified date: February 2022
• Source: Advanced Eye Research Associates
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

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.

Description:

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.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 40
• Est. completion date: December 31, 2022
• Est. primary completion date: December 31, 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 89 Years

Eligibility

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

Related Conditions & MeSH terms

• Diabetic Macular Edema
• Edema
• Macular Edema

Intervention

Drug:
• Aflibercept Injection [Eylea]
Intravitreal injection aflibercept

Locations

Country	Name	City	State
United States	Advanced Eye Centers	South Dartmouth	Massachusetts

Sponsors (1)

Lead Sponsor	Collaborator
Advanced Eye Research Associates

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Measure biomarkers in aqueous humor from individuals with DME	Identify temporal effects of treatment with intravitreal afflibercept	2 years