EC-104 Intravitreal Implant for the Treatment of Diabetic Macular Edema
Condition(s) studied
Investigational drug(s) / intervention(s)
EC-104 high dose: Intravitreal injection
EC-104 low dose: Intravitreal injection
Dexamethasone intravitreal implant: Marketed product intravitreal injection
Study summary
This is a prospective, randomized, subject- and evaluator-masked, Phase 2, multicenter study comparing the safety and efficacy of EC-104-6M high-dose (fluocinolone acetonide \[FA\] 0.14 mg) implant and EC-104-4M low-dose (FA 0.092 mg) implant to Ozurdex® (dexamethasone intravitreal (IVT) implant, 0.7 mg) in subjects with diabetic retinopathy (DR) and center-involving diabetic macular edema (DME), with prior suboptimal clinical response to IVT anti-VEGF therapy who have been previously treated with locally administered corticosteroids without a clinically significant rise in intraocular pressure (IOP).
Eligibility
Primary outcome measure(s)
- Ocular and Systemic Safety — Through Week 24
Incidence of Adverse events
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Retina Associates of Florida, LLC | Tampa | Florida |
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06536491 on ClinicalTrials.gov ↗ ← All trials in the USA