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NCT07449923 · ClinicalTrials.gov registry record · Phase 3
CAPRI: A Phase 3 Randomized, Double-Masked Study Comparing the Efficacy of EYP-1901 Against Aflibercept in DME
A Phase 3 study of Diabetic Macular Edema and Diabetic Macular Edema (DME), sponsored by EyePoint Pharmaceuticals.
- Recruiting
- Registry status
- Phase 3
- Development phase
- 240
- Enrollment target
- 12
- Study locations
NCT07449923 is a Phase 3 study of Diabetic Macular Edema and Diabetic Macular Edema (DME) that is actively recruiting participants, run by EyePoint Pharmaceuticals. The registered enrollment target is 240 participants, below the 3,791-participant average among 63 other Diabetic Macular Edema trials with a reported enrollment target (94% lower). The trial reports 12 study locations across 11 states.
The verdict
NCT07449923, a Phase 3 study of Diabetic Macular Edema and Diabetic Macular Edema (DME), is actively recruiting participants, sponsored by EyePoint Pharmaceuticals.
- RECRUITING
- Registry status
- Phase 3
- Development phase
- 240 participants
- Enrollment target
- 12
- Study locations
Study Summary
This is a phase 3 randomized, double -masked study comparing the efficacy of EYP-1901 against Aflibercept.
Conditions Studied
Interventions
- DRUG EYP-1901
- DRUG Aflibercept (2.0 mg)
Study Locations (12)
Florida
- Retina Specialty Institute - Pensacola
- Retina Vitreous Associates of Florida - Saint Petersburg - St. Petersburg
Arizona
- Phoenix Retina Clinical Trials, LLC - North Phoenix - Phoenix
California
- Retinal Consultants Medical Group - Modesto - Modesto
Colorado
- Retina Specialists of Colorado - Arvada - Arvada
Connecticut
- Coastal Eye Surgeons, LLC - Greenwich
Indiana
- Associated Vitreoretinal & Uveitis Consultants - Carmel - Carmel
Maryland
- Mid Atlantic Retina Specialists - Hagerstown - Hagerstown
North Carolina
- Graystone Eye - Hickory Office - Hickory
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 240 participants |
| Start Date | 2026-02-09 |
| Est. Completion | 2028-08 |
| Phase | Phase 3 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07449923
The ClinicalTrials.gov registry entry for NCT07449923 describes a study currently listed as recruiting, categorized as Phase 3. The registered enrollment target is 240 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 3,791-participant average among 63 other Diabetic Macular Edema trials with a reported enrollment target (94% lower). The listed sponsor is EyePoint Pharmaceuticals, which has 16 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Diabetic Macular Edema appearing as the primary indexed condition, and to 2 interventions - of which EYP-1901 is the first listed.
NCT07449923 reports 12 study locations spanning 11 distinct geographic areas - top geographies include Florida, Arizona, California.
Frequently Asked Questions
What is clinical trial NCT07449923 about?
NCT07449923 is a clinical study titled "CAPRI: A Phase 3 Randomized, Double-Masked Study Comparing the Efficacy of EYP-1901 Against Aflibercept in DME". This is a phase 3 randomized, double -masked study comparing the efficacy of EYP-1901 against Aflibercept.
What is the current status of trial NCT07449923?
This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 240 participants. The study started on 2026-02-09. Estimated completion is 2028-08.
What conditions does trial NCT07449923 study?
This clinical trial studies the following conditions: Diabetic Macular Edema, Diabetic Macular Edema (DME), DME.
What interventions are being tested in trial NCT07449923?
The interventions under investigation include: EYP-1901 (DRUG), Aflibercept (2.0 mg) (DRUG).
Who is sponsoring clinical trial NCT07449923?
This trial is sponsored by EyePoint Pharmaceuticals, which has 16 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07449923 being conducted?
This trial has 12 study locations across Arizona, California, Colorado, Connecticut, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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