drugset / Trial / NCT03126786

Suprachoroidal CLS-TA With Intravitreal Aflibercept Versus Aflibercept Alone in Subject With Diabetic Macular Edema

NCT03126786

Phase 2 Completed 71 enrolled Clearside Biomedical, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this trial is to evaluate the safety and efficacy of suprachoroidal CLS-TA used with intravitreal aflibercept in subjects with DME.

Timeline

Start
2017-07-11
Primary completion
2018-04-17
Completion
2018-04-17

Drugs

EvaluationDrugModalityDoseRoute
Comparator Aflibercept Protein / enzyme biologic 2 mg Intravitreal
Comparator CLS-TA Unknown 4 mg Subcutaneous