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Active, not recruiting Phase 1/2

EC-104 Intravitreal Implant for the Treatment of Diabetic Macular Edema

NCT06536491 · tracked via the Priya Life Science USA tracker
Sponsor
Eclipse Life Sciences, Inc
Phase
Phase 1/2
Started
2024-08-19
Last updated
2026-09-15

Condition(s) studied

Diabetic Macular Edema

Investigational drug(s) / intervention(s)

EC-104 high doseEC-104 low doseDexamethasone intravitreal implant →

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

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Males or females who are at least 18 years of age at the time of informed consent 2. Willing and able to provide signed informed consent (participant or legally authorized representative) prior to any study-related procedures and to comply with all study visits and cooperate with all examinations 3. Diagnosis of diabetes mellitus (Type 1 or Type 2), with history of diabetic macular edema (DME) \< = years duration prior to Screening Visit 1 4. Currently monitored hemoglobin A1c values ≤ 10.0 while under the care of a qualified medical provider for diabetes mellitus management, unless provider allows value variance Inclusion criteria for the study eye (all of the below criteria must be met in the same eye): 5. Early Treatment Diabetic Retinopathy Study BCVA score ≤ 70 letters (Snellen equivalent 20/40 or worse) and ≥ 20 letters (Snellen equivalent 20/400) in at least 1 eye Exclusion Criteria: 1. Previous or current diagnosis of any form of glaucoma (defined as cup-to-disc ratio \> 0.7) or ocular hypertension (documented intraocular pressure (IOP) \> 21 mm Hg without glaucomatous disc damage) requiring medical or surgical intervention 2. History of steroid-induced IOP elevation \> 25 mm Hg 3. Presence of active proliferative diabetic retinopathy, defined as active neovascularization of disc (NVD), neovascularization elsewhere (NVE), neovascularization of iris (NVI), neovascularization of angle (NVA), or vitreous hemorrhage in the setting of active NVD or NVE

Primary outcome measure(s)

  • Ocular and Systemic Safety — Through Week 24
    Incidence of Adverse events

Trial sites (1)

FacilityCityRegionStatus
Retina Associates of Florida, LLC Tampa Florida
Official registry record

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