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NCT03297684

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

Status unknown Last updated 18 February 2022
What this trial tests

trial testing Aflibercept Injection [Eylea] in Diabetic Macular Edema in 40 participants. Status unknown.

Timeline
11 April 2018
Primary endpoint
31 December 2022
31 December 2022

Quick facts

Lead sponsorAdvanced Eye Research Associates
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment40
Start date11 April 2018
Primary completion31 December 2022
Estimated completion31 December 2022
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Advanced Eye Research Associates

Who can join

Adults 18 to 89, any sex, with Diabetic Macular Edema. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Aflibercept Injection [Eylea]

Trials testing the same drug.

Other recruiting trials for Diabetic Macular Edema

Currently open trials in the same condition.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03297684.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing